| geneid | 114827 |
|---|---|
| ensemblid | ENSG00000142621.21 |
| hgncid | 29408 |
| symbol | FHAD1 |
| name | forkhead associated phosphopeptide binding domain 1 |
| refseq_nuc | NM_001391957.1 |
| refseq_prot | NP_001378886.1 |
| ensembl_nuc | ENST00000688493.1 |
| ensembl_prot | ENSP00000509124.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 15247223 |
| end | 15398328 |
| strand | + |
| ver | v1.2 |
| region | chr1:15247223-15398328 |
| region5000 | chr1:15242223-15403328 |
| regionname0 | FHAD1_chr1_15247223_15398328 |
| regionname5000 | FHAD1_chr1_15242223_15403328 |
| 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 | 1479 | 75 | 10 | 15 | 29 | 3 | 16 | 19 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002 | 0/0 | 1479 | 33 | 9 | 3 | 14 | 2 | 5 | 10 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003 | 0/0 | 1479 | 22 | 3 | 5 | 12 | 0 | 2 | 7 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0004 | 0/0 | 1479 | 21 | 4 | 4 | 12 | 0 | 1 | 7 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0005 | 0/0 | 1479 | 15 | 2 | 4 | 2 | 3 | 4 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0006 | 0/0 | 1479 | 9 | 0 | 1 | 7 | 0 | 1 | 5 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0007 | 0/0 | 1479 | 9 | 7 | 2 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0008 | 0/0 | 1479 | 8 | 1 | 0 | 6 | 0 | 1 | 6 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0009 | 0/0 | 1479 | 8 | 1 | 4 | 1 | 0 | 2 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0010 | 0/0 | 1479 | 5 | 0 | 4 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0011 | 0/0 | 1479 | 5 | 0 | 0 | 5 | 0 | 0 | 2 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0012 | 0/0 | 1479 | 5 | 2 | 2 | 0 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0013 | 0/0 | 1479 | 4 | 0 | 1 | 1 | 0 | 2 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0014 | 0/0 | 1479 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0015 | 0/0 | 1479 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0016 | 0/0 | 1479 | 3 | 2 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0017 | 0/0 | 1479 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0018 | 0/0 | 1479 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0019 | 0/0 | 1479 | 3 | 1 | 0 | 2 | 0 | 0 | 2 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0020 | 0/0 | 1479 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0021 | 0/0 | 1479 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0022 | 0/0 | 1479 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0023 | 0/0 | 1479 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0024 | 0/0 | 1479 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0025 | 0/0 | 1479 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0026 | 0/0 | 1479 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0027 | 0/0 | 1479 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0028 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0029 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0030 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0031 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0032 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0033 | 0/0 | 1479 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0034 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0035 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0036 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0037 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0038 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0039 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0040 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0041 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0042 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0043 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0044 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0045 | 0/0 | 1479 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0046 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0047 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0048 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0049 | 0/0 | 1435 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0050 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0051 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0052 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0053 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0054 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0055 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0056 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0057 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0058 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0059 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0060 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0061 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0062 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0063 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0064 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0065 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0066 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0067 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0068 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 4440 | 26 | 3 | 7 | 12 | 0 | 4 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0002 | 1/0 | 4440 | 23 | 2 | 2 | 12 | 1 | 5 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0003 | 0/0 | 4440 | 15 | 2 | 1 | 9 | 1 | 2 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0004 | 0/0 | 4440 | 15 | 0 | 4 | 10 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0005 | 0/0 | 4440 | 8 | 1 | 2 | 1 | 3 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0006 | 0/0 | 4440 | 8 | 1 | 0 | 6 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0007 | 0/0 | 4440 | 6 | 0 | 1 | 4 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0008 | 0/0 | 4440 | 5 | 0 | 0 | 2 | 0 | 3 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0009 | 0/0 | 4440 | 5 | 0 | 0 | 5 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0010 | 0/0 | 4440 | 4 | 1 | 0 | 1 | 2 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0011 | 0/0 | 4440 | 4 | 1 | 0 | 1 | 0 | 2 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0012 | 0/0 | 4440 | 4 | 4 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0013 | 0/1 | 4440 | 4 | 0 | 2 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0014 | 0/0 | 4440 | 4 | 0 | 1 | 2 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0015 | 0/0 | 4440 | 3 | 0 | 3 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0016 | 0/0 | 4440 | 3 | 0 | 1 | 1 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0017 | 0/0 | 4440 | 3 | 3 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0018 | 0/0 | 4440 | 3 | 3 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0019 | 0/0 | 4440 | 3 | 1 | 0 | 1 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0020 | 0/0 | 4440 | 3 | 3 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0021 | 0/0 | 4440 | 3 | 0 | 1 | 1 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0022 | 0/0 | 4440 | 3 | 1 | 0 | 2 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0023 | 0/0 | 4440 | 3 | 0 | 0 | 3 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0024 | 0/0 | 4440 | 3 | 0 | 0 | 3 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0025 | 0/0 | 4440 | 2 | 0 | 0 | 2 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0026 | 0/0 | 4440 | 2 | 0 | 2 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0027 | 0/0 | 4440 | 2 | 2 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0028 | 0/0 | 4440 | 2 | 0 | 2 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0029 | 0/0 | 4440 | 2 | 0 | 1 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0030 | 0/0 | 4440 | 2 | 0 | 0 | 0 | 0 | 2 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0031 | 0/0 | 4440 | 2 | 2 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0032 | 0/0 | 4440 | 2 | 2 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0033 | 0/0 | 4440 | 2 | 2 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0034 | 0/0 | 4440 | 2 | 0 | 0 | 2 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0035 | 0/0 | 4440 | 2 | 1 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0036 | 0/0 | 4440 | 2 | 0 | 1 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0037 | 0/0 | 4440 | 2 | 0 | 2 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0038 | 0/0 | 4440 | 2 | 2 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0039 | 0/0 | 4440 | 2 | 0 | 0 | 0 | 0 | 2 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0040 | 0/0 | 4440 | 2 | 1 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0041 | 0/0 | 4440 | 2 | 0 | 2 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0042 | 0/0 | 4440 | 2 | 0 | 2 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0043 | 0/0 | 4440 | 2 | 0 | 2 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0044 | 0/0 | 4440 | 2 | 0 | 0 | 1 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0045 | 0/0 | 4440 | 2 | 0 | 0 | 2 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0046 | 0/0 | 4440 | 2 | 0 | 0 | 2 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0047 | 0/0 | 4440 | 2 | 0 | 0 | 2 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0048 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0049 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0050 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0051 | 0/0 | 4440 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0052 | 0/0 | 4463 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0053 | 0/0 | 4440 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0054 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0055 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0056 | 0/0 | 4440 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0057 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0058 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0059 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0060 | 0/0 | 4440 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0061 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0062 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0063 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0064 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0065 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0066 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0067 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0068 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0069 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0070 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0071 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0072 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0073 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0074 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0075 | 0/0 | 4440 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0076 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0077 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0078 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0079 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0080 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0081 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0082 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0083 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0084 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0085 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0086 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0087 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0088 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0089 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0090 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0091 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0092 | 0/0 | 4440 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0093 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0094 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0095 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0096 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0097 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0098 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0099 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0100 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0101 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0102 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0103 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0104 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0105 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0106 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0107 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0108 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0109 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0110 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0111 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0112 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0113 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0114 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0115 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0116 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0117 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0118 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0119 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0120 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0121 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0122 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0123 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0124 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0125 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0126 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0127 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0128 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0129 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0130 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0131 | 0/0 | 4440 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0132 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0133 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| c0134 | 0/0 | 4440 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| 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 | 1/0 | 1103 | 41 | 1 | 12 | 16 | 3 | 8 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0002 | 0/0 | 1105 | 21 | 1 | 3 | 15 | 0 | 2 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0003 | 0/0 | 1102 | 21 | 4 | 5 | 11 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0004 | 0/0 | 1103 | 19 | 1 | 2 | 12 | 1 | 3 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0005 | 0/0 | 1103 | 17 | 0 | 3 | 10 | 0 | 4 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0006 | 0/0 | 1102 | 16 | 3 | 2 | 10 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0007 | 0/0 | 1103 | 16 | 14 | 2 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0008 | 0/0 | 1105 | 14 | 1 | 0 | 10 | 0 | 3 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0009 | 0/0 | 1103 | 13 | 1 | 2 | 8 | 0 | 2 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0010 | 0/0 | 1105 | 8 | 0 | 1 | 0 | 2 | 5 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0011 | 0/1 | 1102 | 8 | 2 | 3 | 0 | 0 | 2 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0012 | 0/0 | 1104 | 8 | 2 | 1 | 2 | 0 | 3 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0013 | 0/0 | 1104 | 7 | 2 | 4 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0014 | 0/0 | 1103 | 7 | 4 | 3 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0015 | 0/0 | 1104 | 6 | 1 | 3 | 1 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0016 | 0/0 | 1103 | 5 | 5 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0017 | 0/0 | 1103 | 4 | 0 | 2 | 1 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0018 | 0/0 | 1104 | 4 | 4 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0019 | 0/0 | 1104 | 4 | 4 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0020 | 0/0 | 1101 | 3 | 0 | 2 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0021 | 0/0 | 1103 | 3 | 3 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0022 | 0/0 | 1103 | 3 | 3 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0023 | 0/0 | 1103 | 2 | 2 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0024 | 0/0 | 1103 | 2 | 2 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0025 | 0/0 | 1103 | 2 | 0 | 0 | 0 | 0 | 2 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0026 | 0/0 | 1103 | 2 | 2 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0027 | 0/0 | 1104 | 2 | 2 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0028 | 0/0 | 1105 | 2 | 0 | 0 | 1 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0029 | 0/0 | 1104 | 2 | 1 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0030 | 0/0 | 1105 | 2 | 1 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0031 | 0/0 | 1103 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0032 | 0/0 | 1105 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0033 | 0/0 | 1103 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0034 | 0/0 | 1102 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0035 | 0/0 | 1103 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0036 | 0/0 | 1102 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0037 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0038 | 0/0 | 1105 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0039 | 0/0 | 1103 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0040 | 0/0 | 1103 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0041 | 0/0 | 1103 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0042 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0043 | 0/0 | 1103 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0044 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0045 | 0/0 | 1102 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0046 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0047 | 0/0 | 1103 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0048 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0049 | 0/0 | 1103 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0050 | 0/0 | 1102 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0051 | 0/0 | 1103 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0052 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0053 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0054 | 0/0 | 1103 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0055 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0056 | 0/0 | 1102 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0057 | 0/0 | 1105 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0058 | 0/0 | 1102 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0059 | 0/0 | 1103 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| t0060 | 0/0 | 1105 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0117 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0266 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4440 | 26 | 3 | 7 | 12 | 0 | 4 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0002 | 1/0 | 4440 | 23 | 2 | 2 | 12 | 1 | 5 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0008 | 0/0 | 4440 | 5 | 0 | 0 | 2 | 0 | 3 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0010 | 0/0 | 4440 | 4 | 1 | 0 | 1 | 2 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0013 | 0/1 | 4440 | 4 | 0 | 2 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0015 | 0/0 | 4440 | 3 | 0 | 3 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0032 | 0/0 | 4440 | 2 | 2 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0036 | 0/0 | 4440 | 2 | 0 | 1 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0039 | 0/0 | 4440 | 2 | 0 | 0 | 0 | 0 | 2 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0090 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0092 | 0/0 | 4440 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0102 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0108 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0003 | 0/0 | 4440 | 15 | 2 | 1 | 9 | 1 | 2 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0007 | 0/0 | 4440 | 6 | 0 | 1 | 4 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0018 | 0/0 | 4440 | 3 | 3 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0019 | 0/0 | 4440 | 3 | 1 | 0 | 1 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0035 | 0/0 | 4440 | 2 | 1 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0053 | 0/0 | 4440 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0080 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0081 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0134 | 0/0 | 4440 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0006 | 0/0 | 4440 | 8 | 1 | 0 | 6 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0009 | 0/0 | 4440 | 5 | 0 | 0 | 5 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0026 | 0/0 | 4440 | 2 | 0 | 2 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0037 | 0/0 | 4440 | 2 | 0 | 2 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0055 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0056 | 0/0 | 4440 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0085 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0086 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0098 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0004c0004 | 0/0 | 4440 | 15 | 0 | 4 | 10 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0004c0038 | 0/0 | 4440 | 2 | 2 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0004c0057 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0004c0058 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0004c0087 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0004c0096 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0005c0005 | 0/0 | 4440 | 8 | 1 | 2 | 1 | 3 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0005c0016 | 0/0 | 4440 | 3 | 0 | 1 | 1 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0005c0030 | 0/0 | 4440 | 2 | 0 | 0 | 0 | 0 | 2 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0005c0070 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0005c0072 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0006c0014 | 0/0 | 4440 | 4 | 0 | 1 | 2 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0006c0024 | 0/0 | 4440 | 3 | 0 | 0 | 3 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0006c0045 | 0/0 | 4440 | 2 | 0 | 0 | 2 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0007c0012 | 0/0 | 4440 | 4 | 4 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0007c0033 | 0/0 | 4440 | 2 | 2 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0007c0059 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0007c0082 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0007c0101 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0008c0044 | 0/0 | 4440 | 2 | 0 | 0 | 1 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0008c0047 | 0/0 | 4440 | 2 | 0 | 0 | 2 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0008c0122 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0008c0123 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0008c0125 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0008c0132 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0009c0011 | 0/0 | 4440 | 4 | 1 | 0 | 1 | 0 | 2 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0009c0028 | 0/0 | 4440 | 2 | 0 | 2 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0009c0050 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0009c0071 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0010c0029 | 0/0 | 4440 | 2 | 0 | 1 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0010c0043 | 0/0 | 4440 | 2 | 0 | 2 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0010c0074 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0011c0025 | 0/0 | 4440 | 2 | 0 | 0 | 2 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0011c0034 | 0/0 | 4440 | 2 | 0 | 0 | 2 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0011c0099 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0012c0041 | 0/0 | 4440 | 2 | 0 | 2 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0012c0051 | 0/0 | 4440 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0012c0079 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0012c0097 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0013c0021 | 0/0 | 4440 | 3 | 0 | 1 | 1 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0013c0060 | 0/0 | 4440 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0014c0110 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0014c0112 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0014c0118 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0015c0023 | 0/0 | 4440 | 3 | 0 | 0 | 3 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0016c0040 | 0/0 | 4440 | 2 | 1 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0016c0107 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0017c0017 | 0/0 | 4440 | 3 | 3 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0018c0020 | 0/0 | 4440 | 3 | 3 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0019c0022 | 0/0 | 4440 | 3 | 1 | 0 | 2 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0020c0111 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0020c0116 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0021c0113 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0021c0117 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0022c0046 | 0/0 | 4440 | 2 | 0 | 0 | 2 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0023c0127 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0023c0130 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0024c0027 | 0/0 | 4440 | 2 | 2 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0025c0042 | 0/0 | 4440 | 2 | 0 | 2 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0026c0031 | 0/0 | 4440 | 2 | 2 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0027c0054 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0027c0094 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0028c0109 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0029c0114 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0030c0115 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0031c0119 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0032c0120 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0033c0131 | 0/0 | 4440 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0034c0133 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0035c0124 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0036c0121 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0037c0128 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0038c0129 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0039c0126 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0040c0077 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0041c0076 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0042c0069 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0043c0068 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0044c0073 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0045c0075 | 0/0 | 4440 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0046c0078 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0047c0089 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0048c0091 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0049c0052 | 0/0 | 4463 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0050c0093 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0051c0100 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0052c0088 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0053c0095 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0054c0084 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0055c0083 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0056c0103 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0057c0105 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0058c0106 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0059c0104 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0060c0065 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0061c0066 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0062c0062 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0063c0067 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0064c0063 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0065c0064 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0066c0061 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0067c0049 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0068c0048 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 5544 | 9 | 1 | 1 | 7 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0001t0008 | 0/0 | 5544 | 5 | 0 | 0 | 4 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0001t0010 | 0/0 | 5544 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0001t0012 | 0/0 | 5543 | 3 | 0 | 1 | 0 | 0 | 2 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0001t0013 | 0/0 | 5543 | 5 | 1 | 3 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0001t0014 | 0/0 | 5542 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0001t0015 | 0/0 | 5543 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0001t0057 | 0/0 | 5544 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0002t0001 | 1/0 | 5542 | 18 | 0 | 2 | 10 | 1 | 4 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0002t0009 | 0/0 | 5542 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0002t0018 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0002t0031 | 0/0 | 5542 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0002t0044 | 0/0 | 5543 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0002t0049 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0008t0002 | 0/0 | 5544 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0008t0008 | 0/0 | 5544 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0008t0012 | 0/0 | 5543 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0008t0025 | 0/0 | 5542 | 2 | 0 | 0 | 0 | 0 | 2 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0010t0001 | 0/0 | 5542 | 3 | 1 | 0 | 0 | 2 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0010t0009 | 0/0 | 5542 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0013t0001 | 0/0 | 5542 | 3 | 0 | 2 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0013t0011 | 0/1 | 5541 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0015t0001 | 0/0 | 5542 | 3 | 0 | 3 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0032t0014 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0032t0023 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0036t0002 | 0/0 | 5544 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0036t0008 | 0/0 | 5544 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0039t0001 | 0/0 | 5542 | 2 | 0 | 0 | 0 | 0 | 2 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0090t0048 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0092t0002 | 0/0 | 5544 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0102t0012 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0001c0108t0001 | 0/0 | 5542 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0003t0003 | 0/0 | 5541 | 2 | 0 | 1 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0003t0004 | 0/0 | 5542 | 2 | 0 | 0 | 0 | 1 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0003t0005 | 0/0 | 5542 | 3 | 0 | 0 | 2 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0003t0006 | 0/0 | 5541 | 6 | 1 | 0 | 5 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0003t0014 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0003t0053 | 0/0 | 5543 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0007t0003 | 0/0 | 5541 | 2 | 0 | 0 | 2 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0007t0005 | 0/0 | 5542 | 2 | 0 | 0 | 2 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0007t0006 | 0/0 | 5541 | 2 | 0 | 1 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0018t0007 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0018t0018 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0018t0021 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0019t0004 | 0/0 | 5542 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0019t0006 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0019t0027 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0035t0006 | 0/0 | 5541 | 2 | 1 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0053t0020 | 0/0 | 5540 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0080t0019 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0081t0058 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0002c0134t0003 | 0/0 | 5541 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0006t0002 | 0/0 | 5544 | 5 | 0 | 0 | 5 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0006t0008 | 0/0 | 5544 | 2 | 0 | 0 | 1 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0006t0013 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0009t0001 | 0/0 | 5542 | 3 | 0 | 0 | 3 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0009t0009 | 0/0 | 5542 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0009t0028 | 0/0 | 5544 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0026t0001 | 0/0 | 5542 | 2 | 0 | 2 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0037t0001 | 0/0 | 5542 | 2 | 0 | 2 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0055t0012 | 0/0 | 5543 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0056t0001 | 0/0 | 5542 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0085t0055 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0086t0009 | 0/0 | 5542 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0003c0098t0029 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0004c0004t0004 | 0/0 | 5542 | 10 | 0 | 2 | 8 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0004c0004t0005 | 0/0 | 5542 | 3 | 0 | 0 | 2 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0004c0004t0007 | 0/0 | 5542 | 2 | 0 | 2 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0004c0038t0007 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0004c0038t0014 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0004c0057t0005 | 0/0 | 5542 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0004c0058t0006 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0004c0087t0046 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0004c0096t0002 | 0/0 | 5544 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0005c0005t0010 | 0/0 | 5544 | 3 | 0 | 0 | 0 | 2 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0005c0005t0015 | 0/0 | 5543 | 5 | 1 | 2 | 1 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0005c0016t0028 | 0/0 | 5544 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0005c0016t0032 | 0/0 | 5544 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0005c0016t0033 | 0/0 | 5542 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0005c0030t0010 | 0/0 | 5544 | 2 | 0 | 0 | 0 | 0 | 2 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0005c0070t0035 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0005c0072t0010 | 0/0 | 5544 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0006c0014t0003 | 0/0 | 5541 | 2 | 0 | 0 | 2 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0006c0014t0005 | 0/0 | 5542 | 2 | 0 | 1 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0006c0024t0003 | 0/0 | 5541 | 2 | 0 | 0 | 2 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0006c0024t0005 | 0/0 | 5542 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0006c0045t0003 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0006c0045t0004 | 0/0 | 5542 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0007c0012t0016 | 0/0 | 5542 | 2 | 2 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0007c0012t0026 | 0/0 | 5542 | 2 | 2 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0007c0033t0007 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0007c0033t0014 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0007c0059t0014 | 0/0 | 5542 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0007c0082t0016 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0007c0101t0014 | 0/0 | 5542 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0008c0044t0009 | 0/0 | 5542 | 2 | 0 | 0 | 1 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0008c0047t0009 | 0/0 | 5542 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0008c0047t0059 | 0/0 | 5542 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0008c0122t0009 | 0/0 | 5542 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0008c0123t0012 | 0/0 | 5543 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0008c0125t0012 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0008c0132t0060 | 0/0 | 5544 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0009c0011t0011 | 0/0 | 5541 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0009c0011t0017 | 0/0 | 5542 | 2 | 0 | 0 | 1 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0009c0011t0019 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0009c0028t0011 | 0/0 | 5541 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0009c0028t0020 | 0/0 | 5540 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0009c0050t0020 | 0/0 | 5540 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0009c0071t0017 | 0/0 | 5542 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0010c0029t0017 | 0/0 | 5542 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0010c0029t0036 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0010c0043t0005 | 0/0 | 5542 | 2 | 0 | 2 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0010c0074t0011 | 0/0 | 5541 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0011c0025t0003 | 0/0 | 5541 | 2 | 0 | 0 | 2 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0011c0034t0006 | 0/0 | 5541 | 2 | 0 | 0 | 2 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0011c0099t0006 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0012c0041t0003 | 0/0 | 5541 | 2 | 0 | 2 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0012c0051t0011 | 0/0 | 5541 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0012c0079t0027 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0012c0097t0003 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0013c0021t0002 | 0/0 | 5544 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0013c0021t0008 | 0/0 | 5544 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0013c0021t0013 | 0/0 | 5543 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0013c0060t0001 | 0/0 | 5542 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0014c0110t0008 | 0/0 | 5544 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0014c0112t0007 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0014c0118t0007 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0015c0023t0008 | 0/0 | 5544 | 3 | 0 | 0 | 3 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0016c0040t0005 | 0/0 | 5542 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0016c0040t0021 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0016c0107t0003 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0017c0017t0007 | 0/0 | 5542 | 3 | 3 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0018c0020t0022 | 0/0 | 5542 | 3 | 3 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0019c0022t0004 | 0/0 | 5542 | 2 | 0 | 0 | 2 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0019c0022t0018 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0020c0111t0030 | 0/0 | 5544 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0020c0116t0052 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0021c0113t0016 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0021c0117t0016 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0022c0046t0009 | 0/0 | 5542 | 2 | 0 | 0 | 2 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0023c0127t0019 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0023c0130t0007 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0024c0027t0024 | 0/0 | 5542 | 2 | 2 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0025c0042t0003 | 0/0 | 5541 | 2 | 0 | 2 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0026c0031t0003 | 0/0 | 5541 | 2 | 2 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0027c0054t0009 | 0/0 | 5542 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0027c0094t0001 | 0/0 | 5542 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0028c0109t0007 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0029c0114t0056 | 0/0 | 5541 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0030c0115t0054 | 0/0 | 5542 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0031c0119t0009 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0032c0120t0034 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0033c0131t0005 | 0/0 | 5542 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0034c0133t0003 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0035c0124t0029 | 0/0 | 5543 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0036c0121t0007 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0037c0128t0007 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0038c0129t0007 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0039c0126t0019 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0040c0077t0037 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0041c0076t0038 | 0/0 | 5544 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0042c0069t0023 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0043c0068t0011 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0044c0073t0011 | 0/0 | 5541 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0045c0075t0010 | 0/0 | 5544 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0046c0078t0007 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0047c0089t0050 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0048c0091t0009 | 0/0 | 5542 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0049c0052t0004 | 0/0 | 5565 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0050c0093t0018 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0051c0100t0001 | 0/0 | 5542 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0052c0088t0021 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0053c0095t0006 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0054c0084t0047 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0055c0083t0002 | 0/0 | 5544 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0056c0103t0051 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0057c0105t0004 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0058c0106t0004 | 0/0 | 5542 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0059c0104t0045 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0060c0065t0043 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0061c0066t0040 | 0/0 | 5542 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0062c0062t0011 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0063c0067t0039 | 0/0 | 5542 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0064c0063t0030 | 0/0 | 5544 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0065c0064t0041 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0066c0061t0042 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0067c0049t0005 | 0/0 | 5542 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| a0068c0048t0002 | 0/0 | 5544 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | copy fasta | chr1 | 15242223 | 15403328 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0008g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0008g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0008g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0008g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0008g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0010g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0012g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0012g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0012g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0013g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0013g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0013g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0013g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0013g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0014g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0015g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0001t0057g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0001g0117 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0009g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0018g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0031g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0044g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0002t0049g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0008t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0008t0008g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0008t0012g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0008t0025g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0008t0025g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0010t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0010t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0010t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0010t0009g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0013t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0013t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0013t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0013t0011g0266 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0015t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0015t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0015t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0032t0014g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0032t0023g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0036t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0036t0008g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0039t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0039t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0090t0048g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0092t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0102t0012g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0001c0108t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0003t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0003t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0003t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0003t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0003t0005g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0003t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0003t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0003t0006g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0003t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0003t0006g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0003t0006g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0003t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0003t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0003t0014g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0003t0053g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0007t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0007t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0007t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0007t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0007t0006g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0007t0006g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0018t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0018t0018g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0018t0021g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0019t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0019t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0019t0027g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0035t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0035t0006g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0053t0020g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0080t0019g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0081t0058g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0002c0134t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0006t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0006t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0006t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0006t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0006t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0006t0008g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0006t0008g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0006t0013g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0009t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0009t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0009t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0009t0009g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0009t0028g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0026t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0026t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0037t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0037t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0055t0012g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0056t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0085t0055g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0086t0009g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0003c0098t0029g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0004t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0004t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0004t0004g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0004t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0004t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0004t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0004t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0004t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0004t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0004t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0004t0005g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0004t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0004t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0004t0007g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0004t0007g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0038t0007g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0038t0014g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0057t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0058t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0087t0046g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0004c0096t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0005c0005t0010g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0005c0005t0010g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0005c0005t0010g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0005c0005t0015g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0005c0005t0015g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0005c0005t0015g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0005c0005t0015g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0005c0005t0015g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0005c0016t0028g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0005c0016t0032g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0005c0016t0033g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0005c0030t0010g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0005c0030t0010g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0005c0070t0035g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0005c0072t0010g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0006c0014t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0006c0014t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0006c0014t0005g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0006c0014t0005g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0006c0024t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0006c0024t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0006c0024t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0006c0045t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0006c0045t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0007c0012t0016g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0007c0012t0016g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0007c0012t0026g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0007c0012t0026g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0007c0033t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0007c0033t0014g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0007c0059t0014g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0007c0082t0016g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0007c0101t0014g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0008c0044t0009g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0008c0044t0009g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0008c0047t0009g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0008c0047t0059g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0008c0122t0009g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0008c0123t0012g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0008c0125t0012g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0008c0132t0060g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0009c0011t0011g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0009c0011t0017g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0009c0011t0017g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0009c0011t0019g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0009c0028t0011g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0009c0028t0020g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0009c0050t0020g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0009c0071t0017g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0010c0029t0017g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0010c0029t0036g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0010c0043t0005g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0010c0043t0005g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0010c0074t0011g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0011c0025t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0011c0025t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0011c0034t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0011c0034t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0011c0099t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0012c0041t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0012c0041t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0012c0051t0011g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0012c0079t0027g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0012c0097t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0013c0021t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0013c0021t0008g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0013c0021t0013g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0013c0060t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0014c0110t0008g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0014c0112t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0014c0118t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0015c0023t0008g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0015c0023t0008g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0015c0023t0008g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0016c0040t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0016c0040t0021g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0016c0107t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0017c0017t0007g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0017c0017t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0017c0017t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0018c0020t0022g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0018c0020t0022g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0018c0020t0022g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0019c0022t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0019c0022t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0019c0022t0018g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0020c0111t0030g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0020c0116t0052g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0021c0113t0016g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0021c0117t0016g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0022c0046t0009g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0022c0046t0009g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0023c0127t0019g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0023c0130t0007g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0024c0027t0024g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0024c0027t0024g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0025c0042t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0025c0042t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0026c0031t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0026c0031t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0027c0054t0009g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0027c0094t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0028c0109t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0029c0114t0056g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0030c0115t0054g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0031c0119t0009g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0032c0120t0034g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0033c0131t0005g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0034c0133t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0035c0124t0029g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0036c0121t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0037c0128t0007g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0038c0129t0007g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0039c0126t0019g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0040c0077t0037g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0041c0076t0038g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0042c0069t0023g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0043c0068t0011g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0044c0073t0011g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0045c0075t0010g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0046c0078t0007g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0047c0089t0050g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0048c0091t0009g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0049c0052t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0050c0093t0018g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0051c0100t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0052c0088t0021g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0053c0095t0006g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0054c0084t0047g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0055c0083t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0056c0103t0051g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0057c0105t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0058c0106t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0059c0104t0045g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0060c0065t0043g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0061c0066t0040g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0062c0062t0011g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0063c0067t0039g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0064c0063t0030g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0065c0064t0041g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0066c0061t0042g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0067c0049t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| a0068c0048t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | CHS | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG00423 | hp2 | a0004 | c0004 | t0004 | g0168 | EAS | CHS | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG00438 | hp1 | a0011 | c0025 | t0003 | g0211 | EAS | CHS | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG00438 | hp2 | a0004 | c0004 | t0004 | g0074 | EAS | CHS | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG00544 | hp1 | a0011 | c0025 | t0003 | g0208 | EAS | CHS | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG00544 | hp2 | a0003 | c0006 | t0002 | g0018 | EAS | CHS | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG00558 | hp1 | a0011 | c0099 | t0006 | g0087 | EAS | CHS | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | CHS | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG00609 | hp1 | a0009 | c0011 | t0017 | g0294 | EAS | CHS | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG00609 | hp2 | a0003 | c0006 | t0002 | g0122 | EAS | CHS | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG00621 | hp1 | a0005 | c0016 | t0032 | g0260 | EAS | CHS | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG00621 | hp2 | a0003 | c0009 | t0001 | g0075 | EAS | CHS | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG00642 | hp1 | a0005 | c0005 | t0015 | g0275 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG00642 | hp2 | a0006 | c0014 | t0005 | g0255 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG00673 | hp1 | a0006 | c0024 | t0005 | g0227 | EAS | CHS | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | CHS | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG00735 | hp1 | a0005 | c0072 | t0010 | g0270 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG00735 | hp2 | a0007 | c0059 | t0014 | g0167 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG00738 | hp1 | a0009 | c0028 | t0020 | g0159 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG00738 | hp2 | a0007 | c0101 | t0014 | g0119 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01069 | hp1 | a0025 | c0042 | t0003 | g0010 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01069 | hp2 | a0051 | c0100 | t0001 | g0091 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01070 | hp1 | a0003 | c0086 | t0009 | g0142 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01070 | hp2 | a0004 | c0004 | t0007 | g0002 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01071 | hp1 | a0004 | c0004 | t0007 | g0001 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01071 | hp2 | a0025 | c0042 | t0003 | g0011 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01074 | hp1 | a0009 | c0050 | t0020 | g0114 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01074 | hp2 | a0009 | c0028 | t0011 | g0290 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01081 | hp1 | a0001 | c0013 | t0001 | g0051 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01081 | hp2 | a0009 | c0071 | t0017 | g0291 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01099 | hp1 | a0063 | c0067 | t0039 | g0004 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01099 | hp2 | a0002 | c0035 | t0006 | g0031 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01106 | hp1 | a0061 | c0066 | t0040 | g0003 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01106 | hp2 | a0013 | c0021 | t0013 | g0056 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01109 | hp1 | a0010 | c0074 | t0011 | g0261 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01109 | hp2 | a0064 | c0063 | t0030 | g0195 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01167 | hp1 | a0029 | c0114 | t0056 | g0199 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01167 | hp2 | a0004 | c0004 | t0004 | g0029 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01169 | hp1 | a0001 | c0001 | t0013 | g0028 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01169 | hp2 | a0004 | c0004 | t0004 | g0030 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01192 | hp1 | a0003 | c0026 | t0001 | g0021 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01192 | hp2 | a0001 | c0001 | t0012 | g0128 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01243 | hp1 | a0001 | c0015 | t0001 | g0110 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01243 | hp2 | a0030 | c0115 | t0054 | g0203 | AMR | PUR | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01255 | hp1 | a0010 | c0029 | t0017 | g0276 | AMR | CLM | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01255 | hp2 | a0012 | c0041 | t0003 | g0125 | AMR | CLM | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01256 | hp1 | a0003 | c0037 | t0001 | g0094 | AMR | CLM | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01256 | hp2 | a0001 | c0001 | t0013 | g0092 | AMR | CLM | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01258 | hp1 | a0001 | c0001 | t0013 | g0072 | AMR | CLM | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01258 | hp2 | a0044 | c0073 | t0011 | g0273 | AMR | CLM | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01261 | hp1 | a0012 | c0041 | t0003 | g0124 | AMR | CLM | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01261 | hp2 | a0010 | c0043 | t0005 | g0013 | AMR | CLM | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01361 | hp1 | a0005 | c0005 | t0015 | g0280 | AMR | CLM | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | CLM | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01433 | hp1 | a0010 | c0043 | t0005 | g0012 | AMR | CLM | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01433 | hp2 | a0001 | c0001 | t0015 | g0267 | AMR | CLM | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01496 | hp1 | a0068 | c0048 | t0002 | g0039 | AMR | CLM | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01496 | hp2 | a0001 | c0015 | t0001 | g0109 | AMR | CLM | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01515 | hp1 | a0002 | c0007 | t0006 | g0115 | EUR | IBS | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01515 | hp2 | a0005 | c0005 | t0010 | g0274 | EUR | IBS | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01516 | hp1 | a0001 | c0010 | t0001 | g0097 | EUR | IBS | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01516 | hp2 | a0002 | c0003 | t0004 | g0044 | EUR | IBS | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01517 | hp1 | a0001 | c0010 | t0001 | g0098 | EUR | IBS | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01517 | hp2 | a0005 | c0005 | t0010 | g0277 | EUR | IBS | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01884 | hp1 | a0024 | c0027 | t0024 | g0288 | AFR | ACB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01884 | hp2 | a0004 | c0038 | t0007 | g0143 | AFR | ACB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01928 | hp1 | a0001 | c0015 | t0001 | g0111 | AMR | PEL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01928 | hp2 | a0001 | c0036 | t0002 | g0055 | AMR | PEL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0078 | AMR | PEL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01952 | hp2 | a0002 | c0003 | t0003 | g0133 | AMR | PEL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01975 | hp1 | a0002 | c0007 | t0006 | g0108 | AMR | PEL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01978 | hp1 | a0001 | c0001 | t0014 | g0052 | AMR | PEL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01978 | hp2 | a0003 | c0026 | t0001 | g0106 | AMR | PEL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02015 | hp1 | a0001 | c0001 | t0008 | g0149 | EAS | KHV | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02015 | hp2 | a0002 | c0007 | t0005 | g0210 | EAS | KHV | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02040 | hp1 | a0010 | c0029 | t0036 | g0269 | EAS | KHV | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02040 | hp2 | a0003 | c0009 | t0001 | g0035 | EAS | KHV | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02055 | hp1 | a0002 | c0003 | t0014 | g0151 | AFR | ACB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02055 | hp2 | a0026 | c0031 | t0003 | g0252 | AFR | ACB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02056 | hp1 | a0006 | c0045 | t0004 | g0170 | EAS | KHV | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02056 | hp2 | a0001 | c0008 | t0008 | g0204 | EAS | KHV | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | KHV | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02083 | hp1 | a0027 | c0054 | t0009 | g0206 | EAS | KHV | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02083 | hp2 | a0001 | c0001 | t0008 | g0175 | EAS | KHV | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02132 | hp1 | a0022 | c0046 | t0009 | g0222 | EAS | KHV | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02132 | hp2 | a0016 | c0040 | t0005 | g0137 | EAS | KHV | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02135 | hp1 | a0004 | c0096 | t0002 | g0033 | EAS | KHV | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02135 | hp2 | a0001 | c0010 | t0009 | g0207 | EAS | KHV | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02145 | hp1 | a0016 | c0107 | t0003 | g0145 | AFR | ACB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02145 | hp2 | a0001 | c0002 | t0049 | g0101 | AFR | ACB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02155 | hp1 | a0002 | c0003 | t0006 | g0062 | EAS | CDX | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02155 | hp2 | a0004 | c0004 | t0004 | g0073 | EAS | CDX | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02165 | hp1 | a0027 | c0094 | t0001 | g0082 | EAS | CDX | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02165 | hp2 | a0001 | c0013 | t0001 | g0045 | EAS | CDX | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02257 | hp1 | a0042 | c0069 | t0023 | g0293 | AFR | ACB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02257 | hp2 | a0001 | c0102 | t0012 | g0146 | AFR | ACB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02258 | hp1 | a0066 | c0061 | t0042 | g0007 | AFR | ACB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02258 | hp2 | a0026 | c0031 | t0003 | g0253 | AFR | ACB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02280 | hp1 | a0001 | c0001 | t0057 | g0250 | AFR | ACB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02280 | hp2 | a0046 | c0078 | t0007 | g0232 | AFR | ACB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02293 | hp1 | a0048 | c0091 | t0009 | g0132 | AMR | PEL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02293 | hp2 | a0001 | c0013 | t0001 | g0053 | AMR | PEL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02451 | hp1 | a0057 | c0105 | t0004 | g0059 | AFR | ACB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02451 | hp2 | a0020 | c0116 | t0052 | g0200 | AFR | ACB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02523 | hp1 | a0003 | c0006 | t0008 | g0171 | EAS | KHV | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02523 | hp2 | a0002 | c0003 | t0006 | g0064 | EAS | KHV | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02572 | hp1 | a0014 | c0110 | t0008 | g0254 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02572 | hp2 | a0002 | c0019 | t0027 | g0244 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02602 | hp1 | a0003 | c0006 | t0008 | g0134 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02602 | hp2 | a0002 | c0003 | t0004 | g0017 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02615 | hp1 | a0007 | c0012 | t0016 | g0256 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02615 | hp2 | a0016 | c0040 | t0021 | g0249 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02622 | hp1 | a0001 | c0032 | t0014 | g0152 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02622 | hp2 | a0038 | c0129 | t0007 | g0235 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02630 | hp1 | a0002 | c0018 | t0007 | g0140 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02630 | hp2 | a0062 | c0062 | t0011 | g0285 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02683 | hp1 | a0012 | c0051 | t0011 | g0284 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02683 | hp2 | a0001 | c0001 | t0012 | g0126 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02698 | hp1 | a0005 | c0030 | t0010 | g0265 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02698 | hp2 | a0008 | c0044 | t0009 | g0223 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02717 | hp1 | a0001 | c0032 | t0023 | g0282 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02717 | hp2 | a0001 | c0010 | t0001 | g0182 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02723 | hp1 | a0002 | c0018 | t0021 | g0247 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02723 | hp2 | a0012 | c0079 | t0027 | g0248 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02738 | hp1 | a0006 | c0014 | t0005 | g0220 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0102 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02886 | hp1 | a0012 | c0097 | t0003 | g0141 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02886 | hp2 | a0031 | c0119 | t0009 | g0257 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02896 | hp1 | a0002 | c0080 | t0019 | g0181 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02896 | hp2 | a0007 | c0012 | t0026 | g0245 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02897 | hp1 | a0007 | c0012 | t0026 | g0246 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02897 | hp2 | a0005 | c0070 | t0035 | g0287 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02922 | hp1 | a0007 | c0082 | t0016 | g0180 | AFR | ESN | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02922 | hp2 | a0047 | c0089 | t0050 | g0105 | AFR | ESN | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02965 | hp1 | a0007 | c0033 | t0014 | g0068 | AFR | ESN | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02965 | hp2 | a0018 | c0020 | t0022 | g0241 | AFR | ESN | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02970 | hp1 | a0056 | c0103 | t0051 | g0243 | AFR | ESN | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02970 | hp2 | a0032 | c0120 | t0034 | g0259 | AFR | ESN | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02976 | hp1 | a0001 | c0002 | t0018 | g0156 | AFR | ESN | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02976 | hp2 | a0024 | c0027 | t0024 | g0258 | AFR | ESN | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03017 | hp1 | a0001 | c0036 | t0008 | g0163 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03017 | hp2 | a0001 | c0039 | t0001 | g0036 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03041 | hp1 | a0018 | c0020 | t0022 | g0239 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03041 | hp2 | a0050 | c0093 | t0018 | g0020 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03130 | hp1 | a0043 | c0068 | t0011 | g0292 | AFR | ESN | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03130 | hp2 | a0002 | c0003 | t0006 | g0157 | AFR | ESN | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03139 | hp1 | a0001 | c0001 | t0013 | g0104 | AFR | ESN | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03139 | hp2 | a0004 | c0058 | t0006 | g0183 | AFR | ESN | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03195 | hp1 | a0017 | c0017 | t0007 | g0008 | AFR | ESN | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03195 | hp2 | a0020 | c0111 | t0030 | g0179 | AFR | ESN | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03209 | hp1 | a0017 | c0017 | t0007 | g0148 | AFR | MSL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03209 | hp2 | a0004 | c0038 | t0014 | g0155 | AFR | MSL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03225 | hp1 | a0001 | c0090 | t0048 | g0158 | AFR | MSL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03225 | hp2 | a0021 | c0113 | t0016 | g0194 | AFR | MSL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03453 | hp1 | a0037 | c0128 | t0007 | g0233 | AFR | MSL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03453 | hp2 | a0036 | c0121 | t0007 | g0201 | AFR | MSL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03486 | hp1 | a0003 | c0085 | t0055 | g0139 | AFR | MSL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03486 | hp2 | a0002 | c0081 | t0058 | g0251 | AFR | MSL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03490 | hp1 | a0013 | c0021 | t0002 | g0084 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03490 | hp2 | a0001 | c0008 | t0025 | g0112 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0038 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03491 | hp2 | a0001 | c0039 | t0001 | g0037 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03492 | hp1 | a0001 | c0008 | t0025 | g0113 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0077 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03516 | hp1 | a0007 | c0033 | t0007 | g0138 | AFR | ESN | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03516 | hp2 | a0028 | c0109 | t0007 | g0197 | AFR | ESN | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03540 | hp1 | a0040 | c0077 | t0037 | g0262 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03540 | hp2 | a0007 | c0012 | t0016 | g0187 | AFR | GWD | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03579 | hp1 | a0004 | c0087 | t0046 | g0121 | AFR | MSL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03579 | hp2 | a0014 | c0118 | t0007 | g0198 | AFR | MSL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03654 | hp1 | a0001 | c0002 | t0009 | g0162 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03654 | hp2 | a0001 | c0001 | t0010 | g0281 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03688 | hp1 | a0001 | c0008 | t0012 | g0205 | SAS | STU | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03688 | hp2 | a0004 | c0004 | t0005 | g0164 | SAS | STU | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03704 | hp1 | a0049 | c0052 | t0004 | g0120 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03704 | hp2 | a0009 | c0011 | t0011 | g0272 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03710 | hp1 | a0002 | c0019 | t0004 | g0118 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03710 | hp2 | a0001 | c0001 | t0008 | g0160 | SAS | PJL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03834 | hp1 | a0045 | c0075 | t0010 | g0278 | SAS | BEB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03834 | hp2 | a0001 | c0092 | t0002 | g0100 | SAS | BEB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03927 | hp1 | a0003 | c0056 | t0001 | g0107 | SAS | BEB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03927 | hp2 | a0009 | c0011 | t0017 | g0263 | SAS | BEB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG04115 | hp1 | a0002 | c0053 | t0020 | g0096 | SAS | STU | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG04115 | hp2 | a0013 | c0060 | t0001 | g0166 | SAS | STU | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG04184 | hp1 | a0005 | c0030 | t0010 | g0264 | SAS | BEB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG04184 | hp2 | a0005 | c0016 | t0028 | g0009 | SAS | BEB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG04199 | hp1 | a0002 | c0003 | t0005 | g0135 | SAS | STU | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG04199 | hp2 | a0033 | c0131 | t0005 | g0219 | SAS | STU | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG04204 | hp1 | a0002 | c0134 | t0003 | g0209 | SAS | STU | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG04204 | hp2 | a0001 | c0001 | t0012 | g0161 | SAS | STU | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18612 | hp1 | a0004 | c0004 | t0005 | g0173 | EAS | CHB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18612 | hp2 | a0002 | c0019 | t0006 | g0066 | EAS | CHB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18906 | hp1 | a0060 | c0065 | t0043 | g0005 | AFR | YRI | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18906 | hp2 | a0023 | c0130 | t0007 | g0238 | AFR | YRI | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18943 | hp1 | a0006 | c0014 | t0003 | g0214 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18943 | hp2 | a0001 | c0001 | t0013 | g0048 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18944 | hp1 | a0011 | c0034 | t0006 | g0085 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18944 | hp2 | a0003 | c0009 | t0001 | g0043 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18950 | hp1 | a0004 | c0004 | t0005 | g0174 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18950 | hp2 | a0034 | c0133 | t0003 | g0216 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18956 | hp2 | a0002 | c0007 | t0003 | g0186 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18960 | hp2 | a0015 | c0023 | t0008 | g0130 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18964 | hp1 | a0001 | c0001 | t0008 | g0127 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18964 | hp2 | a0002 | c0007 | t0003 | g0190 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18966 | hp1 | a0008 | c0122 | t0009 | g0215 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18966 | hp2 | a0003 | c0006 | t0002 | g0103 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18968 | hp1 | a0003 | c0009 | t0009 | g0178 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18968 | hp2 | a0001 | c0001 | t0008 | g0129 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18970 | hp2 | a0002 | c0003 | t0005 | g0177 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18971 | hp1 | a0002 | c0003 | t0005 | g0172 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18971 | hp2 | a0055 | c0083 | t0002 | g0047 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18977 | hp1 | a0053 | c0095 | t0006 | g0016 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18977 | hp2 | a0015 | c0023 | t0008 | g0123 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18978 | hp1 | a0003 | c0009 | t0028 | g0191 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18978 | hp2 | a0004 | c0004 | t0004 | g0024 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18981 | hp1 | a0058 | c0106 | t0004 | g0042 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18981 | hp2 | a0013 | c0021 | t0008 | g0136 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18982 | hp1 | a0006 | c0014 | t0003 | g0224 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18982 | hp2 | a0008 | c0123 | t0012 | g0228 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18983 | hp1 | a0005 | c0005 | t0015 | g0283 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18983 | hp2 | a0022 | c0046 | t0009 | g0193 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18984 | hp1 | a0002 | c0003 | t0006 | g0089 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18984 | hp2 | a0008 | c0047 | t0059 | g0230 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18986 | hp2 | a0002 | c0003 | t0006 | g0083 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18991 | hp1 | a0006 | c0024 | t0003 | g0226 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18992 | hp1 | a0019 | c0022 | t0004 | g0022 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18992 | hp2 | a0002 | c0007 | t0005 | g0212 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18994 | hp1 | a0004 | c0004 | t0004 | g0027 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19000 | hp1 | a0003 | c0006 | t0002 | g0090 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19000 | hp2 | a0002 | c0003 | t0003 | g0192 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19002 | hp1 | a0003 | c0006 | t0002 | g0046 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19002 | hp2 | a0006 | c0045 | t0003 | g0225 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19003 | hp1 | a0067 | c0049 | t0005 | g0236 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19005 | hp1 | a0004 | c0004 | t0004 | g0086 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19005 | hp2 | a0011 | c0034 | t0006 | g0034 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19007 | hp1 | a0001 | c0002 | t0031 | g0088 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19009 | hp1 | a0001 | c0008 | t0002 | g0095 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19009 | hp2 | a0001 | c0108 | t0001 | g0165 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19030 | hp1 | a0003 | c0098 | t0029 | g0237 | AFR | LWK | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19030 | hp2 | a0052 | c0088 | t0021 | g0242 | AFR | LWK | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19043 | hp1 | a0008 | c0125 | t0012 | g0196 | AFR | LWK | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19043 | hp2 | a0041 | c0076 | t0038 | g0289 | AFR | LWK | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19055 | hp1 | a0019 | c0022 | t0004 | g0071 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19056 | hp1 | a0001 | c0002 | t0044 | g0169 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19056 | hp2 | a0002 | c0003 | t0006 | g0069 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19064 | hp1 | a0006 | c0024 | t0003 | g0231 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19064 | hp2 | a0004 | c0004 | t0004 | g0067 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19066 | hp1 | a0035 | c0124 | t0029 | g0217 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19077 | hp1 | a0008 | c0047 | t0009 | g0221 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19077 | hp2 | a0015 | c0023 | t0008 | g0131 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19080 | hp2 | a0004 | c0057 | t0005 | g0189 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19081 | hp1 | a0008 | c0132 | t0060 | g0229 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19081 | hp2 | a0008 | c0044 | t0009 | g0218 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19090 | hp1 | a0003 | c0055 | t0012 | g0213 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19090 | hp2 | a0002 | c0003 | t0053 | g0176 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19240 | hp1 | a0002 | c0018 | t0018 | g0153 | AFR | YRI | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA19240 | hp2 | a0002 | c0035 | t0006 | g0026 | AFR | YRI | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0080 | EUR | TSI | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA20752 | hp2 | a0005 | c0005 | t0015 | g0268 | EUR | TSI | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0019 | SAS | GIH | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA20905 | hp2 | a0005 | c0005 | t0010 | g0279 | SAS | GIH | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01123 | hp1 | a0005 | c0016 | t0033 | g0271 | AMR | CLM | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG01123 | hp2 | a0003 | c0037 | t0001 | g0032 | AMR | CLM | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02109 | hp1 | a0005 | c0005 | t0015 | g0286 | AFR | ACB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02109 | hp2 | a0054 | c0084 | t0047 | g0154 | AFR | ACB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02486 | hp1 | a0009 | c0011 | t0019 | g0144 | AFR | ACB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02486 | hp2 | a0017 | c0017 | t0007 | g0147 | AFR | ACB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02559 | hp1 | a0059 | c0104 | t0045 | g0014 | AFR | ACB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG02559 | hp2 | a0003 | c0006 | t0013 | g0060 | AFR | ACB | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03471 | hp1 | a0023 | c0127 | t0019 | g0184 | AFR | MSL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG03471 | hp2 | a0018 | c0020 | t0022 | g0240 | AFR | MSL | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG06807 | hp1 | a0039 | c0126 | t0019 | g0185 | AFR | USA | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| HG06807 | hp2 | a0014 | c0112 | t0007 | g0202 | AFR | USA | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18955 | hp1 | a0004 | c0004 | t0004 | g0116 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | USA | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA20300 | hp2 | a0065 | c0064 | t0041 | g0006 | AFR | USA | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA21309 | hp1 | a0019 | c0022 | t0018 | g0015 | AFR | LWK | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| NA21309 | hp2 | a0021 | c0117 | t0016 | g0234 | AFR | LWK | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0013 | t0011 | g0266 | REF | REF | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0117 | REF | REF | FHAD1_chr1_15242223_15403328 | FHAD1 | chr1 | 15242223 | 15403328 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:15272335
|
G | A | 1 | a0068 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.106G>A | p.Asp36Asn | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/34 | 293/5542 | 106/4440 | 36/1479 | chr1 | 15272335 | ||
| chr1:15272425
|
G | A | 1 | a0067 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.196G>A | p.Glu66Lys | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/34 | 383/5542 | 196/4440 | 66/1479 | chr1 | 15272425 | ||
| chr1:15272525
|
C | T | 19 | a0006a0008a0014others(16): Show | 40 | HG00642.hp2 HG00673.hp1 HG01167.hp1 others(37): Show |
missense_variant | MODERATE | c.296C>T | p.Pro99Leu | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/34 | 483/5542 | 296/4440 | 99/1479 | chr1 | 15272525 | ||
| chr1:15289636
|
G | A | 7 | a0060a0061a0062others(4): Show | 7 | HG01099.hp1 HG01106.hp1 HG01109.hp2 others(4): Show |
missense_variant | MODERATE | c.538G>A | p.Asp180Asn | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/34 | 725/5542 | 538/4440 | 180/1479 | chr1 | 15289636 | ||
| chr1:15289643
|
G | A | 19 | a0005a0009a0010others(16): Show | 50 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(47): Show |
missense_variant | MODERATE | c.545G>A | p.Arg182His | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/34 | 732/5542 | 545/4440 | 182/1479 | chr1 | 15289643 | ||
| chr1:15301280
|
G | A | 12 | a0015a0016a0022others(9): Show | 19 | HG01884.hp1 HG02055.hp2 HG02132.hp1 others(16): Show |
missense_variant | MODERATE | c.754G>A | p.Val252Ile | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/34 | 941/5542 | 754/4440 | 252/1479 | chr1 | 15301280 | ||
| chr1:15301410
|
A | C | 1 | a0045 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.884A>C | p.Lys295Thr | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/34 | 1071/5542 | 884/4440 | 295/1479 | chr1 | 15301410 | ||
| chr1:15313085
|
A | G | 10 | a0013a0019a0023others(7): Show | 16 | HG01106.hp2 HG02451.hp1 HG02559.hp1 others(13): Show |
missense_variant | MODERATE | c.1068A>G | p.Ile356Met | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/34 | 1255/5542 | 1068/4440 | 356/1479 | chr1 | 15313085 | ||
| chr1:15324518
|
G | C | 1 | a0032 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.1432G>C | p.Glu478Gln | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/34 | 1619/5542 | 1432/4440 | 478/1479 | chr1 | 15324518 | ||
| chr1:15327059
|
C | G | 2 | a0018a0056 | 4 | HG02965.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.1474C>G | p.Leu492Val | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 12/34 | 1661/5542 | 1474/4440 | 492/1479 | chr1 | 15327059 | ||
| chr1:15327105
|
C | T | 1 | a0017 | 3 | HG02486.hp2 HG03195.hp1 HG03209.hp1 |
missense_variant | MODERATE | c.1520C>T | p.Ala507Val | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 12/34 | 1707/5542 | 1520/4440 | 507/1479 | chr1 | 15327105 | ||
| chr1:15327134
|
G | A | 1 | a0055 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.1549G>A | p.Asp517Asn | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 12/34 | 1736/5542 | 1549/4440 | 517/1479 | chr1 | 15327134 | ||
| chr1:15339529
|
T | G | 1 | a0039 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1955T>G | p.Met652Arg | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/34 | 2142/5542 | 1955/4440 | 652/1479 | chr1 | 15339529 | ||
| chr1:15341823
|
G | A | 9 | a0012a0026a0036others(6): Show | 14 | HG01109.hp2 HG01255.hp2 HG01261.hp1 others(11): Show |
missense_variant | MODERATE | c.2065G>A | p.Glu689Lys | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/34 | 2252/5542 | 2065/4440 | 689/1479 | chr1 | 15341823 | ||
| chr1:15360563
|
A | G | 19 | a0003a0004a0010others(16): Show | 67 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(64): Show |
missense_variant | MODERATE | c.2822A>G | p.Glu941Gly | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 22/34 | 3009/5542 | 2822/4440 | 941/1479 | chr1 | 15360563 | ||
| chr1:15360674
|
A | G | 2 | a0025a0062 | 3 | HG01069.hp1 HG01071.hp2 HG02630.hp2 |
missense_variant | MODERATE | c.2933A>G | p.Glu978Gly | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 22/34 | 3120/5542 | 2933/4440 | 978/1479 | chr1 | 15360674 | ||
| chr1:15360698
|
A | G | 3 | a0039a0057a0066 | 3 | HG02258.hp1 HG02451.hp1 HG06807.hp1 |
missense_variant | MODERATE | c.2957A>G | p.Asp986Gly | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 22/34 | 3144/5542 | 2957/4440 | 986/1479 | chr1 | 15360698 | ||
| chr1:15367576
|
G | A | 3 | a0029a0047a0060 | 3 | HG01167.hp1 HG02922.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.3268G>A | p.Val1090Ile | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/34 | 3455/5542 | 3268/4440 | 1090/1479 | chr1 | 15367576 | ||
| chr1:15369450
|
C | T | 1 | a0027 | 2 | HG02083.hp1 HG02165.hp1 |
missense_variant | MODERATE | c.3395C>T | p.Thr1132Ile | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/34 | 3582/5542 | 3395/4440 | 1132/1479 | chr1 | 15369450 | ||
| chr1:15374620
|
C | T | 6 | a0007a0017a0021others(3): Show | 17 | HG00735.hp2 HG00738.hp2 HG02257.hp1 others(14): Show |
missense_variant | MODERATE | c.3566C>T | p.Ala1189Val | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/34 | 3753/5542 | 3566/4440 | 1189/1479 | chr1 | 15374620 | ||
| chr1:15374622
|
C | T | 1 | a0059 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.3568C>T | p.Arg1190Cys | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/34 | 3755/5542 | 3568/4440 | 1190/1479 | chr1 | 15374622 | ||
| chr1:15375693
|
C | T | 1 | a0052 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.3668C>T | p.Pro1223Leu | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/34 | 3855/5542 | 3668/4440 | 1223/1479 | chr1 | 15375693 | ||
| chr1:15375729
|
C | A | 1 | a0059 | 1 | HG02559.hp1 | missense_variant&splice_region_variant | MODERATE | c.3704C>A | p.Ala1235Glu | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/34 | 3891/5542 | 3704/4440 | 1235/1479 | chr1 | 15375729 | ||
| chr1:15381279
|
A | G | 1 | a0051 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.3850A>G | p.Met1284Val | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 30/34 | 4037/5542 | 3850/4440 | 1284/1479 | chr1 | 15381279 | ||
| chr1:15381357
|
G | A | 4 | a0024a0030a0054others(1): Show | 5 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(2): Show |
missense_variant | MODERATE | c.3928G>A | p.Asp1310Asn | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 30/34 | 4115/5542 | 3928/4440 | 1310/1479 | chr1 | 15381357 | ||
| chr1:15382044
|
A | G | 46 | a0002a0004a0006others(43): Show | 148 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(145): Show |
missense_variant | MODERATE | c.4039A>G | p.Ile1347Val | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/34 | 4226/5542 | 4039/4440 | 1347/1479 | chr1 | 15382044 | ||
| chr1:15382095
|
G | C | 1 | a0048 | 1 | HG02293.hp1 | missense_variant | MODERATE | c.4090G>C | p.Glu1364Gln | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/34 | 4277/5542 | 4090/4440 | 1364/1479 | chr1 | 15382095 | ||
| chr1:15382156
|
A | G | 1 | a0050 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.4151A>G | p.Gln1384Arg | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/34 | 4338/5542 | 4151/4440 | 1384/1479 | chr1 | 15382156 | ||
| chr1:15391209
|
G | GAGACGAG others(16): Show |
1 | a0049 | 1 | HG03704.hp1 | frameshift_variant&stop_gained | HIGH | c.4270_4292dupAGACGA others(17): Show |
p.Lys1432fs | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/34 | 4480/5542 | 4293/4440 | 1431/1479 | INFO_REALIGN_3_PRIME | chr1 | 15391209 | |
| chr1:15397315
|
T | A | 3 | a0011a0034a0053 | 7 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(4): Show |
missense_variant | MODERATE | c.4342T>A | p.Ser1448Thr | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 34/34 | 4529/5542 | 4342/4440 | 1448/1479 | chr1 | 15397315 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:15272424
|
C | T | 1 | a0002c0134 | 1 | HG04204.hp1 | synonymous_variant | LOW | c.195C>T | p.Asn65Asn | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/34 | 382/5542 | 195/4440 | 65/1479 | chr1 | 15272424 | ||
| chr1:15272529
|
G | A | 19 | a0001c0008a0001c0010a0001c0015others(16): Show | 35 | HG00438.hp1 HG00544.hp1 HG00735.hp2 others(32): Show |
splice_region_variant&synonymous_variant | LOW | c.300G>A | p.Pro100Pro | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/34 | 487/5542 | 300/4440 | 100/1479 | chr1 | 15272529 | ||
| chr1:15289626
|
C | T | 2 | a0010c0043a0025c0042 | 4 | HG01069.hp1 HG01071.hp2 HG01261.hp2 others(1): Show |
synonymous_variant | LOW | c.528C>T | p.Phe176Phe | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/34 | 715/5542 | 528/4440 | 176/1479 | chr1 | 15289626 | ||
| chr1:15289653
|
C | T | 1 | a0012c0041 | 2 | HG01255.hp2 HG01261.hp1 |
synonymous_variant | LOW | c.555C>T | p.Pro185Pro | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/34 | 742/5542 | 555/4440 | 185/1479 | chr1 | 15289653 | ||
| chr1:15296718
|
A | G | 12 | a0001c0108a0006c0024a0008c0047others(9): Show | 19 | HG00673.hp1 HG02132.hp1 HG02132.hp2 others(16): Show |
synonymous_variant | LOW | c.603A>G | p.Ser201Ser | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/34 | 790/5542 | 603/4440 | 201/1479 | chr1 | 15296718 | ||
| chr1:15316416
|
T | C | 10 | a0002c0080a0002c0081a0007c0082others(7): Show | 13 | HG01069.hp1 HG01071.hp2 HG02258.hp1 others(10): Show |
synonymous_variant | LOW | c.1209T>C | p.Ala403Ala | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 9/34 | 1396/5542 | 1209/4440 | 403/1479 | chr1 | 15316416 | ||
| chr1:15324523
|
C | T | 1 | a0033c0131 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.1437C>T | p.Ser479Ser | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/34 | 1624/5542 | 1437/4440 | 479/1479 | chr1 | 15324523 | ||
| chr1:15327067
|
C | T | 21 | a0001c0013a0001c0015a0001c0036others(18): Show | 35 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(32): Show |
synonymous_variant | LOW | c.1482C>T | p.His494His | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 12/34 | 1669/5542 | 1482/4440 | 494/1479 | chr1 | 15327067 | ||
| chr1:15329519
|
C | T | 1 | a0014c0118 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.1884C>T | p.Ile628Ile | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/34 | 2071/5542 | 1884/4440 | 628/1479 | chr1 | 15329519 | ||
| chr1:15341780
|
G | A | 58 | a0001c0013a0001c0015a0001c0032others(55): Show | 80 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(77): Show |
synonymous_variant | LOW | c.2022G>A | p.Gln674Gln | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/34 | 2209/5542 | 2022/4440 | 674/1479 | chr1 | 15341780 | ||
| chr1:15341876
|
G | A | 3 | a0014c0110a0025c0042a0062c0062 | 4 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(1): Show |
synonymous_variant | LOW | c.2118G>A | p.Thr706Thr | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/34 | 2305/5542 | 2118/4440 | 706/1479 | chr1 | 15341876 | ||
| chr1:15345475
|
G | A | 1 | a0003c0098 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.2298G>A | p.Glu766Glu | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/34 | 2485/5542 | 2298/4440 | 766/1479 | chr1 | 15345475 | ||
| chr1:15349098
|
G | A | 1 | a0012c0079 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.2403G>A | p.Ser801Ser | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/34 | 2590/5542 | 2403/4440 | 801/1479 | chr1 | 15349098 | ||
| chr1:15352897
|
G | A | 4 | a0012c0079a0016c0107a0023c0127others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG03471.hp1 others(1): Show |
synonymous_variant | LOW | c.2475G>A | p.Ala825Ala | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/34 | 2662/5542 | 2475/4440 | 825/1479 | chr1 | 15352897 | ||
| chr1:15369442
|
G | A | 1 | a0008c0122 | 1 | NA18966.hp1 | synonymous_variant | LOW | c.3387G>A | p.Thr1129Thr | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/34 | 3574/5542 | 3387/4440 | 1129/1479 | chr1 | 15369442 | ||
| chr1:15375634
|
A | G | 10 | a0002c0035a0002c0053a0002c0081others(7): Show | 13 | HG00738.hp1 HG01074.hp2 HG01099.hp2 others(10): Show |
synonymous_variant | LOW | c.3609A>G | p.Leu1203Leu | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/34 | 3796/5542 | 3609/4440 | 1203/1479 | chr1 | 15375634 | ||
| chr1:15380787
|
T | C | 5 | a0001c0090a0003c0085a0040c0077others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG03225.hp1 others(2): Show |
synonymous_variant | LOW | c.3792T>C | p.Ser1264Ser | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 29/34 | 3979/5542 | 3792/4440 | 1264/1479 | chr1 | 15380787 | ||
| chr1:15382061
|
G | A | 1 | a0005c0072 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.4056G>A | p.Ser1352Ser | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/34 | 4243/5542 | 4056/4440 | 1352/1479 | chr1 | 15382061 | ||
| chr1:15382100
|
C | T | 1 | a0001c0092 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.4095C>T | p.Ala1365Ala | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/34 | 4282/5542 | 4095/4440 | 1365/1479 | chr1 | 15382100 | ||
| chr1:15397347
|
G | A | 23 | a0001c0001a0001c0008a0001c0036others(20): Show | 72 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(69): Show |
synonymous_variant | LOW | c.4374G>A | p.Leu1458Leu | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 34/34 | 4561/5542 | 4374/4440 | 1458/1479 | chr1 | 15397347 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:15247245
|
A | G | 2 | a0008c0047t0059a0008c0132t0060 | 2 | NA18984.hp2 NA19081.hp1 |
5_prime_UTR_variant | MODIFIER | c.-165A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/34 | 4540 | chr1 | 15247245 | |||||
| chr1:15247258
|
G | C | 1 | a0001c0002t0031 | 1 | NA19007.hp1 | 5_prime_UTR_variant | MODIFIER | c.-152G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/34 | 4527 | chr1 | 15247258 | |||||
| chr1:15247262
|
G | A | 28 | a0001c0001t0010a0001c0001t0015a0001c0013t0011others(25): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
5_prime_UTR_variant | MODIFIER | c.-148G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/34 | 4523 | chr1 | 15247262 | |||||
| chr1:15247263
|
C | T | 2 | a0001c0001t0057a0002c0081t0058 | 2 | HG02280.hp1 HG03486.hp2 |
5_prime_UTR_variant | MODIFIER | c.-147C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/34 | 4522 | chr1 | 15247263 | |||||
| chr1:15247272
|
G | A | 5 | a0060c0065t0043a0061c0066t0040a0063c0067t0039others(2): Show | 5 | HG01099.hp1 HG01106.hp1 HG02258.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-138G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/34 | 4513 | chr1 | 15247272 | |||||
| chr1:15247273
|
G | A | 28 | a0001c0001t0010a0001c0001t0015a0001c0013t0011others(25): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
5_prime_UTR_variant | MODIFIER | c.-137G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/34 | 4512 | chr1 | 15247273 | |||||
| chr1:15247279
|
A | G | 119 | a0001c0001t0008a0001c0001t0010a0001c0001t0012others(116): Show | 161 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(158): Show |
5_prime_UTR_variant | MODIFIER | c.-131A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/34 | 4506 | chr1 | 15247279 | |||||
| chr1:15247365
|
G | A | 1 | a0063c0067t0039 | 1 | HG01099.hp1 | 5_prime_UTR_variant | MODIFIER | c.-45G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/34 | 4420 | chr1 | 15247365 | |||||
| chr1:15247391
|
G | C | 8 | a0002c0018t0021a0002c0019t0027a0007c0012t0026others(5): Show | 11 | HG02572.hp2 HG02615.hp2 HG02723.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-19G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/34 | 4394 | chr1 | 15247391 | |||||
| chr1:15397434
|
C | T | 1 | a0001c0008t0025 | 2 | HG03490.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*21C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 34/34 | 21 | chr1 | 15397434 | |||||
| chr1:15397507
|
A | G | 81 | a0001c0002t0018a0001c0002t0049a0001c0013t0011others(78): Show | 119 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*94A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 34/34 | 94 | chr1 | 15397507 | |||||
| chr1:15397537
|
A | G | 154 | a0001c0001t0002a0001c0001t0008a0001c0001t0010others(151): Show | 230 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*124A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 34/34 | 124 | chr1 | 15397537 | |||||
| chr1:15397580
|
T | C | 1 | a0004c0087t0046 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*167T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 34/34 | 167 | chr1 | 15397580 | |||||
| chr1:15397799
|
G | A | 1 | a0020c0116t0052 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*386G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 34/34 | 386 | chr1 | 15397799 | |||||
| chr1:15397932
|
A | G | 15 | a0001c0002t0018a0001c0002t0049a0002c0018t0018others(12): Show | 15 | HG01167.hp1 HG02145.hp2 HG02486.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*519A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 34/34 | 519 | chr1 | 15397932 | |||||
| chr1:15397956
|
A | C | 4 | a0001c0090t0048a0003c0085t0055a0040c0077t0037others(1): Show | 4 | HG02258.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*543A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 34/34 | 543 | chr1 | 15397956 | |||||
| chr1:15398054
|
C | T | 6 | a0007c0012t0016a0007c0012t0026a0007c0082t0016others(3): Show | 8 | HG02615.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*641C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 34/34 | 641 | chr1 | 15398054 | |||||
| chr1:15398127
|
T | TA | 16 | a0001c0002t0018a0001c0002t0044a0002c0018t0018others(13): Show | 16 | HG01109.hp2 HG02486.hp1 HG02572.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*729dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 34/34 | 730 | INFO_REALIGN_3_PRIME | chr1 | 15398127 | ||||
| chr1:15398127
|
TA | T | 38 | a0001c0013t0011a0002c0003t0003a0002c0003t0006others(35): Show | 55 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*729delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 34/34 | 729 | INFO_REALIGN_3_PRIME | chr1 | 15398127 | ||||
| chr1:15398205
|
A | G | 15 | a0001c0002t0018a0001c0002t0049a0002c0018t0018others(12): Show | 15 | HG01167.hp1 HG02145.hp2 HG02486.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*792A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 34/34 | 792 | chr1 | 15398205 | |||||
| chr1:15398251
|
T | C | 4 | a0001c0090t0048a0003c0085t0055a0040c0077t0037others(1): Show | 4 | HG02258.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*838T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 34/34 | 838 | chr1 | 15398251 | |||||
| chr1:15398276
|
C | CA | 30 | a0001c0001t0012a0001c0001t0013a0001c0001t0015others(27): Show | 41 | HG00642.hp1 HG01106.hp2 HG01109.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*881dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 34/34 | 882 | INFO_REALIGN_3_PRIME | chr1 | 15398276 | ||||
| chr1:15398276
|
C | CAA | 24 | a0001c0001t0002a0001c0001t0008a0001c0001t0010others(21): Show | 46 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*880_*881dupAA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 34/34 | 882 | INFO_REALIGN_3_PRIME | chr1 | 15398276 | ||||
| chr1:15398276
|
CA | C | 8 | a0002c0053t0020a0009c0028t0020a0009c0050t0020others(5): Show | 8 | HG00738.hp1 HG01074.hp1 HG01167.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*881delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 34/34 | 881 | INFO_REALIGN_3_PRIME | chr1 | 15398276 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:15247454
|
A | C | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-15+59A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15247454 | ||||||
| chr1:15247546
|
C | T | 1 | a0031c0119t0009g0257 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-15+151C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15247546 | ||||||
| chr1:15247580
|
C | T | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-15+185C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15247580 | ||||||
| chr1:15247685
|
A | C | 1 | a0007c0012t0016g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-15+290A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15247685 | ||||||
| chr1:15247742
|
C | G | 1 | a0006c0014t0005g0255 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-15+347C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15247742 | ||||||
| chr1:15247826
|
C | T | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-15+431C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15247826 | ||||||
| chr1:15248049
|
G | T | 1 | a0014c0110t0008g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-15+654G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15248049 | ||||||
| chr1:15248051
|
C | CT | 70 | a0001c0001t0057g0250a0001c0002t0001g0188a0001c0008t0008g0204others(67): Show | 70 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.-15+670dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | INFO_REALIGN_3_PRIME | chr1 | 15248051 | |||||
| chr1:15248225
|
G | C | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-15+830G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15248225 | ||||||
| chr1:15248397
|
C | CT | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-15+1003dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | INFO_REALIGN_3_PRIME | chr1 | 15248397 | |||||
| chr1:15248505
|
C | A | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-15+1110C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15248505 | ||||||
| chr1:15248517
|
A | C | 1 | a0007c0012t0016g0187 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-15+1122A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15248517 | ||||||
| chr1:15248579
|
C | CT | 29 | a0001c0001t0057g0250a0001c0010t0001g0182a0002c0007t0003g0186others(26): Show | 29 | HG00642.hp2 HG02055.hp2 HG02258.hp2 others(26): Show |
intron_variant | MODIFIER | c.-15+1200dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | INFO_REALIGN_3_PRIME | chr1 | 15248579 | |||||
| chr1:15248579
|
C | T | 36 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(33): Show | 36 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.-15+1184C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15248579 | ||||||
| chr1:15248734
|
A | T | 121 | a0001c0001t0008g0175a0001c0001t0010g0281a0001c0001t0015g0267others(118): Show | 121 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.-15+1339A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15248734 | ||||||
| chr1:15248790
|
G | A | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-15+1395G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15248790 | ||||||
| chr1:15248811
|
C | T | 1 | a0006c0045t0004g0170 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-15+1416C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15248811 | ||||||
| chr1:15248853
|
G | T | 1 | a0009c0011t0017g0294 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-15+1458G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15248853 | ||||||
| chr1:15248856
|
A | G | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-15+1461A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15248856 | ||||||
| chr1:15248948
|
C | G | 1 | a0001c0002t0044g0169 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-15+1553C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15248948 | ||||||
| chr1:15248987
|
G | A | 2 | a0002c0007t0003g0190a0004c0057t0005g0189 | 2 | NA18964.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.-15+1592G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15248987 | ||||||
| chr1:15249084
|
G | C | 10 | a0001c0001t0008g0175a0002c0003t0003g0192a0002c0003t0005g0172others(7): Show | 10 | HG02083.hp2 HG02523.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-15+1689G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15249084 | ||||||
| chr1:15249221
|
A | G | 1 | a0004c0004t0004g0168 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-15+1826A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15249221 | ||||||
| chr1:15249290
|
TA | T | 109 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0001t0057g0250others(106): Show | 109 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.-15+1910delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | INFO_REALIGN_3_PRIME | chr1 | 15249290 | |||||
| chr1:15249316
|
C | T | 36 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(33): Show | 36 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.-15+1921C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15249316 | ||||||
| chr1:15249486
|
T | C | 3 | a0021c0117t0016g0234a0037c0128t0007g0233a0038c0129t0007g0235 | 3 | HG02622.hp2 HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-15+2091T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15249486 | ||||||
| chr1:15249561
|
T | C | 2 | a0004c0004t0007g0001a0004c0004t0007g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-15+2166T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15249561 | ||||||
| chr1:15249609
|
A | G | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-2162A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15249609 | ||||||
| chr1:15249644
|
A | T | 5 | a0001c0001t0008g0160a0001c0001t0012g0161a0001c0002t0009g0162others(2): Show | 5 | HG03017.hp1 HG03654.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-2127A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15249644 | ||||||
| chr1:15249743
|
C | T | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-2028C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15249743 | ||||||
| chr1:15249746
|
C | G | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-2025C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15249746 | ||||||
| chr1:15249774
|
C | T | 1 | a0009c0028t0020g0159 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-14-1997C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15249774 | ||||||
| chr1:15249775
|
C | A | 5 | a0060c0065t0043g0005a0061c0066t0040g0003a0063c0067t0039g0004others(2): Show | 5 | HG01099.hp1 HG01106.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-1996C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15249775 | ||||||
| chr1:15249815
|
C | T | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-1956C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15249815 | ||||||
| chr1:15249865
|
G | A | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-1906G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15249865 | ||||||
| chr1:15249909
|
G | A | 1 | a0005c0016t0032g0260 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-14-1862G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15249909 | ||||||
| chr1:15249945
|
G | A | 47 | a0001c0008t0008g0204a0001c0008t0012g0205a0001c0010t0009g0207others(44): Show | 47 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.-14-1826G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15249945 | ||||||
| chr1:15250068
|
A | C | 5 | a0001c0001t0057g0250a0002c0081t0058g0251a0026c0031t0003g0252others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-1703A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15250068 | ||||||
| chr1:15250082
|
C | T | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-1689C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15250082 | ||||||
| chr1:15250093
|
C | T | 8 | a0001c0002t0018g0156a0001c0032t0014g0152a0001c0090t0048g0158others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14-1678C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15250093 | ||||||
| chr1:15250126
|
C | T | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-1645C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15250126 | ||||||
| chr1:15250129
|
A | G | 1 | a0001c0002t0001g0150 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-14-1642A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15250129 | ||||||
| chr1:15250139
|
A | C | 1 | a0001c0001t0008g0149 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-14-1632A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15250139 | ||||||
| chr1:15250170
|
T | A | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-1601T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15250170 | ||||||
| chr1:15250287
|
T | C | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-1484T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15250287 | ||||||
| chr1:15250292
|
T | C | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-1479T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15250292 | ||||||
| chr1:15250526
|
A | G | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-1245A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15250526 | ||||||
| chr1:15250529
|
A | G | 7 | a0001c0102t0012g0146a0004c0004t0007g0001a0004c0004t0007g0002others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14-1242A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15250529 | ||||||
| chr1:15250550
|
A | T | 45 | a0001c0008t0008g0204a0001c0008t0012g0205a0001c0010t0009g0207others(42): Show | 45 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.-14-1221A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15250550 | ||||||
| chr1:15250624
|
A | G | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-1147A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15250624 | ||||||
| chr1:15250782
|
C | T | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-989C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15250782 | ||||||
| chr1:15250877
|
T | C | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-894T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15250877 | ||||||
| chr1:15250961
|
G | C | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-810G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15250961 | ||||||
| chr1:15250984
|
A | G | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-787A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15250984 | ||||||
| chr1:15251119
|
C | T | 70 | a0001c0001t0057g0250a0001c0008t0008g0204a0001c0008t0012g0205others(67): Show | 70 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.-14-652C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15251119 | ||||||
| chr1:15251144
|
G | A | 35 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(32): Show | 35 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-14-627G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15251144 | ||||||
| chr1:15251218
|
T | C | 1 | a0007c0012t0016g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-14-553T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15251218 | ||||||
| chr1:15251284
|
AACAAAAA others(4): Show |
A | 6 | a0002c0018t0007g0140a0003c0085t0055g0139a0003c0086t0009g0142others(3): Show | 6 | HG01070.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-486_-14-476del others(11): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15251284 | ||||||
| chr1:15251286
|
C | A | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-485C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15251286 | ||||||
| chr1:15251287
|
A | AC | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-484_-14-483ins others(1): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15251287 | ||||||
| chr1:15251294
|
AC | A | 31 | a0001c0001t0008g0160a0001c0001t0008g0175a0001c0001t0012g0161others(28): Show | 31 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.-14-475delC | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | INFO_REALIGN_3_PRIME | chr1 | 15251294 | |||||
| chr1:15251294
|
ACC | A | 70 | a0001c0001t0057g0250a0001c0008t0008g0204a0001c0008t0012g0205others(67): Show | 70 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.-14-476_-14-475del others(2): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15251294 | ||||||
| chr1:15251295
|
C | A | 38 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(35): Show | 38 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.-14-476C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15251295 | ||||||
| chr1:15251406
|
T | C | 1 | a0022c0046t0009g0193 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-14-365T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15251406 | ||||||
| chr1:15251434
|
C | T | 19 | a0006c0014t0003g0214a0006c0014t0003g0224a0006c0014t0005g0220others(16): Show | 19 | HG00673.hp1 HG02132.hp1 HG02698.hp2 others(16): Show |
intron_variant | MODIFIER | c.-14-337C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15251434 | ||||||
| chr1:15251535
|
TTTGA | T | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-233_-14-230del others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | INFO_REALIGN_3_PRIME | chr1 | 15251535 | |||||
| chr1:15251598
|
A | G | 11 | a0002c0018t0021g0247a0002c0019t0027g0244a0007c0012t0026g0245others(8): Show | 11 | HG02572.hp2 HG02615.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.-14-173A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15251598 | ||||||
| chr1:15251618
|
C | T | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-153C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15251618 | ||||||
| chr1:15251626
|
T | C | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-145T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15251626 | ||||||
| chr1:15251675
|
G | C | 2 | a0019c0022t0018g0015a0059c0104t0045g0014 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-14-96G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15251675 | ||||||
| chr1:15251699
|
T | C | 145 | a0001c0001t0008g0160a0001c0001t0008g0175a0001c0001t0010g0281others(142): Show | 145 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.-14-72T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 1/33 | chr1 | 15251699 | ||||||
| chr1:15252017
|
A | G | 40 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0008g0149others(37): Show | 40 | HG01069.hp1 HG01070.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.93+140A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15252017 | ||||||
| chr1:15252068
|
G | A | 1 | a0006c0014t0003g0214 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.93+191G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15252068 | ||||||
| chr1:15252320
|
C | T | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.93+443C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15252320 | ||||||
| chr1:15252408
|
A | G | 71 | a0001c0001t0057g0250a0001c0008t0008g0204a0001c0008t0012g0205others(68): Show | 71 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.93+531A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15252408 | ||||||
| chr1:15252471
|
A | G | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.93+594A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15252471 | ||||||
| chr1:15252476
|
A | G | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.93+599A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15252476 | ||||||
| chr1:15252519
|
T | C | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.93+642T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15252519 | ||||||
| chr1:15252535
|
C | G | 6 | a0002c0018t0007g0140a0003c0085t0055g0139a0003c0086t0009g0142others(3): Show | 6 | HG01070.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.93+658C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15252535 | ||||||
| chr1:15252537
|
G | GGACTA | 6 | a0002c0018t0007g0140a0003c0085t0055g0139a0003c0086t0009g0142others(3): Show | 6 | HG01070.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.93+660_93+661insGA others(3): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15252537 | ||||||
| chr1:15252538
|
T | G | 6 | a0002c0018t0007g0140a0003c0085t0055g0139a0003c0086t0009g0142others(3): Show | 6 | HG01070.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.93+661T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15252538 | ||||||
| chr1:15252840
|
A | G | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.93+963A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15252840 | ||||||
| chr1:15252874
|
G | A | 37 | a0001c0001t0010g0281a0001c0001t0015g0267a0001c0013t0011g0266others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.93+997G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15252874 | ||||||
| chr1:15253006
|
C | T | 63 | a0001c0008t0008g0204a0001c0008t0012g0205a0001c0010t0009g0207others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.93+1129C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253006 | ||||||
| chr1:15253101
|
C | G | 1 | a0003c0006t0002g0122 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.93+1224C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253101 | ||||||
| chr1:15253148
|
C | CTG | 35 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0012g0126others(32): Show | 35 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.93+1307_93+1308dup others(2): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15253148 | |||||
| chr1:15253148
|
C | CTGTG | 19 | a0001c0001t0008g0175a0001c0001t0012g0161a0001c0002t0009g0162others(16): Show | 19 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.93+1305_93+1308dup others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15253148 | |||||
| chr1:15253148
|
C | CTGTGTG | 10 | a0002c0003t0005g0177a0002c0003t0053g0176a0002c0080t0019g0181others(7): Show | 10 | HG02486.hp2 HG02896.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.93+1303_93+1308dup others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15253148 | |||||
| chr1:15253148
|
C | CTGTGTGT others(3): Show |
1 | a0001c0001t0008g0149 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.93+1299_93+1308dup others(10): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15253148 | |||||
| chr1:15253148
|
CTG | C | 116 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(113): Show | 116 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.93+1307_93+1308del others(2): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15253148 | |||||
| chr1:15253148
|
CTGTG | C | 20 | a0001c0002t0001g0019a0002c0003t0004g0017a0003c0006t0002g0018others(17): Show | 20 | HG00544.hp2 HG00642.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.93+1305_93+1308del others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15253148 | |||||
| chr1:15253148
|
CTGTGTG | C | 13 | a0002c0018t0021g0247a0002c0019t0027g0244a0007c0012t0026g0245others(10): Show | 13 | HG00738.hp1 HG02572.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.93+1303_93+1308del others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15253148 | |||||
| chr1:15253148
|
CTGTGTGT others(7): Show |
C | 1 | a0008c0122t0009g0215 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.93+1295_93+1308del others(14): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15253148 | |||||
| chr1:15253186
|
C | G | 30 | a0001c0001t0010g0281a0001c0032t0023g0282a0005c0005t0010g0274others(27): Show | 30 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.93+1309C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253186 | ||||||
| chr1:15253187
|
A | T | 30 | a0001c0001t0010g0281a0001c0032t0023g0282a0005c0005t0010g0274others(27): Show | 30 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.93+1310A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253187 | ||||||
| chr1:15253189
|
A | T | 30 | a0001c0001t0010g0281a0001c0032t0023g0282a0005c0005t0010g0274others(27): Show | 30 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.93+1312A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253189 | ||||||
| chr1:15253190
|
G | C | 23 | a0001c0001t0010g0281a0001c0032t0023g0282a0005c0005t0010g0274others(20): Show | 23 | HG00609.hp1 HG00642.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.93+1313G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253190 | ||||||
| chr1:15253190
|
G | GTC | 5 | a0005c0016t0032g0260a0009c0028t0011g0290a0009c0071t0017g0291others(2): Show | 5 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+1313_93+1314ins others(2): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253190 | ||||||
| chr1:15253192
|
A | G | 30 | a0001c0001t0010g0281a0001c0032t0023g0282a0005c0005t0010g0274others(27): Show | 30 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.93+1315A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253192 | ||||||
| chr1:15253192
|
AAGAG | A | 7 | a0001c0001t0015g0267a0001c0013t0011g0266a0005c0030t0010g0264others(4): Show | 7 | HG01109.hp1 HG01433.hp2 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.93+1324_93+1327del others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15253192 | |||||
| chr1:15253196
|
G | A | 30 | a0001c0001t0010g0281a0001c0032t0023g0282a0005c0005t0010g0274others(27): Show | 30 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.93+1319G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253196 | ||||||
| chr1:15253225
|
A | G | 2 | a0017c0017t0007g0147a0017c0017t0007g0148 | 2 | HG02486.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.93+1348A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253225 | ||||||
| chr1:15253251
|
C | A | 257 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(254): Show | 257 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(254): Show |
intron_variant | MODIFIER | c.93+1374C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253251 | ||||||
| chr1:15253283
|
C | T | 185 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(182): Show | 185 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(182): Show |
intron_variant | MODIFIER | c.93+1406C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253283 | ||||||
| chr1:15253306
|
C | T | 256 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(253): Show | 256 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(253): Show |
intron_variant | MODIFIER | c.93+1429C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253306 | ||||||
| chr1:15253342
|
C | A | 10 | a0002c0018t0021g0247a0002c0019t0027g0244a0007c0012t0026g0245others(7): Show | 10 | HG02572.hp2 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.93+1465C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253342 | ||||||
| chr1:15253387
|
C | A | 1 | a0019c0022t0018g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.93+1510C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253387 | ||||||
| chr1:15253436
|
A | G | 1 | a0001c0092t0002g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.93+1559A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253436 | ||||||
| chr1:15253445
|
A | T | 1 | a0001c0001t0002g0099 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.93+1568A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253445 | ||||||
| chr1:15253526
|
G | A | 7 | a0002c0019t0027g0244a0016c0040t0021g0249a0018c0020t0022g0239others(4): Show | 7 | HG02572.hp2 HG02615.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+1649G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253526 | ||||||
| chr1:15253561
|
T | G | 256 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(253): Show | 256 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(253): Show |
intron_variant | MODIFIER | c.93+1684T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253561 | ||||||
| chr1:15253734
|
T | C | 25 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0008g0160others(22): Show | 25 | HG01069.hp1 HG01071.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.93+1857T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253734 | ||||||
| chr1:15253765
|
A | T | 1 | a0004c0004t0004g0116 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.93+1888A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253765 | ||||||
| chr1:15253804
|
T | C | 118 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(115): Show | 118 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.93+1927T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253804 | ||||||
| chr1:15253838
|
G | T | 261 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(258): Show | 261 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(258): Show |
intron_variant | MODIFIER | c.93+1961G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253838 | ||||||
| chr1:15253875
|
C | T | 6 | a0002c0018t0007g0140a0003c0085t0055g0139a0003c0086t0009g0142others(3): Show | 6 | HG01070.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.93+1998C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253875 | ||||||
| chr1:15253935
|
G | A | 2 | a0001c0010t0001g0182a0004c0058t0006g0183 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.93+2058G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253935 | ||||||
| chr1:15253947
|
T | A | 1 | a0007c0012t0016g0187 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.93+2070T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15253947 | ||||||
| chr1:15254063
|
G | A | 1 | a0002c0003t0004g0017 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.93+2186G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254063 | ||||||
| chr1:15254248
|
T | C | 1 | a0011c0025t0003g0211 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.93+2371T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254248 | ||||||
| chr1:15254271
|
G | A | 256 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(253): Show | 256 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(253): Show |
intron_variant | MODIFIER | c.93+2394G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254271 | ||||||
| chr1:15254390
|
G | A | 1 | a0017c0017t0007g0008 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.93+2513G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254390 | ||||||
| chr1:15254391
|
G | A | 256 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(253): Show | 256 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(253): Show |
intron_variant | MODIFIER | c.93+2514G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254391 | ||||||
| chr1:15254454
|
G | A | 2 | a0008c0044t0009g0218a0035c0124t0029g0217 | 2 | NA19066.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.93+2577G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254454 | ||||||
| chr1:15254506
|
C | T | 24 | a0001c0001t0008g0160a0001c0001t0012g0161a0001c0002t0009g0162others(21): Show | 24 | HG01069.hp1 HG01070.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.93+2629C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254506 | ||||||
| chr1:15254508
|
G | GGGT | 256 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(253): Show | 256 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(253): Show |
intron_variant | MODIFIER | c.93+2631_93+2632ins others(3): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254508 | ||||||
| chr1:15254537
|
G | A | 1 | a0005c0005t0015g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.93+2660G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254537 | ||||||
| chr1:15254560
|
G | C | 256 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(253): Show | 256 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(253): Show |
intron_variant | MODIFIER | c.93+2683G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254560 | ||||||
| chr1:15254567
|
A | G | 2 | a0017c0017t0007g0147a0017c0017t0007g0148 | 2 | HG02486.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.93+2690A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254567 | ||||||
| chr1:15254578
|
T | C | 256 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(253): Show | 256 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(253): Show |
intron_variant | MODIFIER | c.93+2701T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254578 | ||||||
| chr1:15254629
|
C | G | 1 | a0003c0037t0001g0094 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.93+2752C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254629 | ||||||
| chr1:15254631
|
G | A | 256 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(253): Show | 256 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(253): Show |
intron_variant | MODIFIER | c.93+2754G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254631 | ||||||
| chr1:15254638
|
G | C | 11 | a0001c0001t0008g0149a0001c0001t0008g0175a0002c0003t0003g0192others(8): Show | 11 | HG02015.hp1 HG02083.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.93+2761G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254638 | ||||||
| chr1:15254719
|
A | G | 7 | a0001c0001t0057g0250a0002c0081t0058g0251a0003c0098t0029g0237others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.93+2842A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254719 | ||||||
| chr1:15254765
|
C | A | 63 | a0001c0008t0008g0204a0001c0008t0012g0205a0001c0010t0009g0207others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.93+2888C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254765 | ||||||
| chr1:15254828
|
G | C | 186 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(183): Show | 186 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.93+2951G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254828 | ||||||
| chr1:15254877
|
G | T | 2 | a0042c0069t0023g0293a0043c0068t0011g0292 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.93+3000G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254877 | ||||||
| chr1:15254910
|
C | T | 186 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(183): Show | 186 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.93+3033C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254910 | ||||||
| chr1:15254915
|
A | G | 186 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(183): Show | 186 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.93+3038A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15254915 | ||||||
| chr1:15255037
|
C | T | 186 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(183): Show | 186 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.93+3160C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15255037 | ||||||
| chr1:15255120
|
T | TAAAAAAA others(3): Show |
25 | a0001c0001t0002g0093a0001c0001t0008g0127a0001c0001t0008g0129others(22): Show | 25 | HG01069.hp2 HG01070.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.93+3249_93+3250ins others(10): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15255120 | |||||
| chr1:15255120
|
T | TAAAAAAA others(4): Show |
161 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(158): Show | 161 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.93+3249_93+3250ins others(11): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15255120 | |||||
| chr1:15255132
|
C | A | 186 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(183): Show | 186 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.93+3255C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15255132 | ||||||
| chr1:15255270
|
T | G | 1 | a0033c0131t0005g0219 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.93+3393T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15255270 | ||||||
| chr1:15255298
|
C | T | 2 | a0001c0010t0001g0097a0001c0010t0001g0098 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.93+3421C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15255298 | ||||||
| chr1:15255337
|
T | C | 70 | a0001c0001t0057g0250a0001c0008t0008g0204a0001c0008t0012g0205others(67): Show | 70 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.93+3460T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15255337 | ||||||
| chr1:15255383
|
T | A | 5 | a0005c0016t0028g0009a0010c0043t0005g0012a0010c0043t0005g0013others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+3506T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15255383 | ||||||
| chr1:15255504
|
T | C | 1 | a0010c0029t0036g0269 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.93+3627T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15255504 | ||||||
| chr1:15255527
|
G | A | 166 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(163): Show | 166 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.93+3650G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15255527 | ||||||
| chr1:15255575
|
C | T | 186 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(183): Show | 186 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.93+3698C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15255575 | ||||||
| chr1:15255679
|
T | G | 1 | a0006c0014t0003g0214 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.93+3802T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15255679 | ||||||
| chr1:15255681
|
C | CA | 186 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(183): Show | 186 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.93+3804_93+3805ins others(1): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15255681 | ||||||
| chr1:15255681
|
C | T | 1 | a0023c0130t0007g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.93+3804C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15255681 | ||||||
| chr1:15255682
|
G | A | 186 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(183): Show | 186 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.93+3805G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15255682 | ||||||
| chr1:15255944
|
AG | A | 5 | a0001c0102t0012g0146a0004c0004t0007g0001a0004c0004t0007g0002others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.93+4069delG | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15255944 | |||||
| chr1:15255973
|
CTGCCTTG | C | 94 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(91): Show | 94 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.93+4100_93+4106del others(7): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15255973 | |||||
| chr1:15256201
|
A | G | 52 | a0001c0008t0008g0204a0001c0008t0012g0205a0001c0010t0009g0207others(49): Show | 52 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.93+4324A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15256201 | ||||||
| chr1:15256315
|
T | A | 2 | a0001c0002t0001g0023a0019c0022t0004g0022 | 2 | NA18992.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.93+4438T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15256315 | ||||||
| chr1:15256329
|
G | C | 7 | a0001c0102t0012g0146a0004c0004t0007g0001a0004c0004t0007g0002others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.93+4452G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15256329 | ||||||
| chr1:15256390
|
C | T | 11 | a0001c0001t0008g0149a0001c0001t0008g0175a0002c0003t0003g0192others(8): Show | 11 | HG02015.hp1 HG02083.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.93+4513C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15256390 | ||||||
| chr1:15256509
|
C | T | 1 | a0012c0079t0027g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.93+4632C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15256509 | ||||||
| chr1:15256645
|
C | CA | 22 | a0002c0007t0003g0186a0002c0018t0021g0247a0003c0098t0029g0237others(19): Show | 22 | HG00609.hp1 HG00735.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.93+4795dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15256645 | |||||
| chr1:15256645
|
CA | C | 15 | a0001c0001t0008g0160a0001c0002t0001g0025a0001c0002t0009g0162others(12): Show | 15 | HG01081.hp2 HG01106.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.93+4795delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15256645 | |||||
| chr1:15256645
|
CAA | C | 120 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(117): Show | 120 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.93+4794_93+4795del others(2): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15256645 | |||||
| chr1:15256645
|
CAAA | C | 12 | a0001c0001t0002g0093a0001c0001t0008g0149a0001c0001t0008g0175others(9): Show | 12 | HG02015.hp1 HG02083.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.93+4793_93+4795del others(3): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15256645 | |||||
| chr1:15256645
|
CAAAAAAA others(3): Show |
C | 4 | a0005c0005t0015g0286a0005c0070t0035g0287a0040c0077t0037g0262others(1): Show | 4 | HG02109.hp1 HG02897.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.93+4786_93+4795del others(10): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15256645 | |||||
| chr1:15256645
|
CAAAAAAA others(4): Show |
C | 1 | a0015c0023t0008g0123 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.93+4785_93+4795del others(11): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15256645 | |||||
| chr1:15256645
|
CAAAAAAA others(5): Show |
C | 14 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0012g0126others(11): Show | 14 | HG01192.hp2 HG01255.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.93+4784_93+4795del others(12): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15256645 | |||||
| chr1:15256645
|
CAAAAAAA others(8): Show |
C | 23 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(20): Show | 23 | HG00735.hp2 HG00738.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.93+4781_93+4795del others(15): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15256645 | |||||
| chr1:15256645
|
CAAAAAAA others(9): Show |
C | 1 | a0002c0053t0020g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.93+4780_93+4795del others(16): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15256645 | |||||
| chr1:15256676
|
T | C | 5 | a0005c0016t0028g0009a0010c0043t0005g0012a0010c0043t0005g0013others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+4799T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15256676 | ||||||
| chr1:15256720
|
A | G | 2 | a0017c0017t0007g0147a0017c0017t0007g0148 | 2 | HG02486.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.93+4843A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15256720 | ||||||
| chr1:15256773
|
A | G | 256 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(253): Show | 256 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(253): Show |
intron_variant | MODIFIER | c.93+4896A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15256773 | ||||||
| chr1:15256945
|
T | C | 256 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(253): Show | 256 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(253): Show |
intron_variant | MODIFIER | c.93+5068T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15256945 | ||||||
| chr1:15257092
|
T | C | 1 | a0007c0012t0016g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.93+5215T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15257092 | ||||||
| chr1:15257115
|
T | C | 256 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(253): Show | 256 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(253): Show |
intron_variant | MODIFIER | c.93+5238T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15257115 | ||||||
| chr1:15257148
|
G | A | 24 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.93+5271G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15257148 | ||||||
| chr1:15257196
|
T | C | 6 | a0001c0001t0057g0250a0002c0081t0058g0251a0007c0012t0016g0256others(3): Show | 6 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.93+5319T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15257196 | ||||||
| chr1:15257199
|
G | A | 4 | a0002c0080t0019g0181a0007c0012t0016g0187a0007c0082t0016g0180others(1): Show | 4 | HG02896.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+5322G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15257199 | ||||||
| chr1:15257323
|
C | T | 186 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(183): Show | 186 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.93+5446C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15257323 | ||||||
| chr1:15257349
|
A | G | 1 | a0012c0079t0027g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.93+5472A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15257349 | ||||||
| chr1:15257583
|
C | T | 186 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(183): Show | 186 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.93+5706C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15257583 | ||||||
| chr1:15257851
|
G | C | 16 | a0001c0001t0008g0149a0001c0001t0008g0175a0002c0003t0003g0192others(13): Show | 16 | HG01099.hp1 HG01106.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.93+5974G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15257851 | ||||||
| chr1:15257989
|
G | A | 2 | a0001c0090t0048g0158a0002c0003t0006g0157 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.93+6112G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15257989 | ||||||
| chr1:15258268
|
C | CA | 4 | a0002c0080t0019g0181a0007c0012t0016g0187a0007c0082t0016g0180others(1): Show | 4 | HG02896.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+6391_93+6392ins others(1): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15258268 | ||||||
| chr1:15258268
|
C | T | 1 | a0005c0016t0028g0009 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.93+6391C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15258268 | ||||||
| chr1:15258282
|
A | T | 11 | a0001c0001t0008g0149a0001c0001t0008g0175a0002c0003t0003g0192others(8): Show | 11 | HG02015.hp1 HG02083.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.93+6405A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15258282 | ||||||
| chr1:15258313
|
A | G | 2 | a0017c0017t0007g0147a0017c0017t0007g0148 | 2 | HG02486.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.93+6436A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15258313 | ||||||
| chr1:15258337
|
C | T | 5 | a0006c0014t0005g0255a0021c0117t0016g0234a0023c0130t0007g0238others(2): Show | 5 | HG00642.hp2 HG02622.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.93+6460C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15258337 | ||||||
| chr1:15258345
|
C | T | 3 | a0003c0086t0009g0142a0004c0038t0007g0143a0012c0097t0003g0141 | 3 | HG01070.hp1 HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.93+6468C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15258345 | ||||||
| chr1:15258407
|
C | T | 3 | a0001c0002t0001g0025a0001c0002t0031g0088a0002c0003t0006g0089 | 3 | HG02071.hp1 NA18984.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.93+6530C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15258407 | ||||||
| chr1:15258582
|
C | CT | 11 | a0001c0002t0018g0156a0002c0007t0005g0210a0002c0080t0019g0181others(8): Show | 11 | HG00558.hp1 HG02015.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.93+6706dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15258582 | |||||
| chr1:15258582
|
CTCT | C | 11 | a0001c0001t0008g0149a0001c0001t0008g0175a0002c0003t0003g0192others(8): Show | 11 | HG02015.hp1 HG02083.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.93+6707_93+6709del others(3): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15258582 | |||||
| chr1:15258583
|
TC | T | 25 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(22): Show | 25 | HG00735.hp2 HG00738.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.93+6707delC | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15258583 | ||||||
| chr1:15258584
|
C | T | 237 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(234): Show | 237 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.93+6707C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15258584 | ||||||
| chr1:15258714
|
C | T | 1 | a0004c0058t0006g0183 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.93+6837C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15258714 | ||||||
| chr1:15258731
|
A | C | 1 | a0009c0050t0020g0114 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.93+6854A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15258731 | ||||||
| chr1:15258752
|
A | AT | 256 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(253): Show | 256 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(253): Show |
intron_variant | MODIFIER | c.93+6882dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15258752 | |||||
| chr1:15258830
|
C | T | 4 | a0002c0080t0019g0181a0007c0012t0016g0187a0007c0082t0016g0180others(1): Show | 4 | HG02896.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+6953C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15258830 | ||||||
| chr1:15258867
|
T | G | 70 | a0001c0001t0057g0250a0001c0008t0008g0204a0001c0008t0012g0205others(67): Show | 70 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.93+6990T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15258867 | ||||||
| chr1:15258974
|
T | C | 2 | a0002c0035t0006g0026a0050c0093t0018g0020 | 2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.93+7097T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15258974 | ||||||
| chr1:15258984
|
A | T | 2 | a0023c0127t0019g0184a0039c0126t0019g0185 | 2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.93+7107A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15258984 | ||||||
| chr1:15259088
|
G | A | 1 | a0004c0004t0004g0027 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.93+7211G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15259088 | ||||||
| chr1:15259097
|
G | T | 186 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(183): Show | 186 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.93+7220G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15259097 | ||||||
| chr1:15259117
|
T | G | 25 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(22): Show | 25 | HG00735.hp2 HG00738.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.93+7240T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15259117 | ||||||
| chr1:15259149
|
T | A | 70 | a0001c0001t0057g0250a0001c0008t0008g0204a0001c0008t0012g0205others(67): Show | 70 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.93+7272T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15259149 | ||||||
| chr1:15259205
|
A | G | 5 | a0001c0001t0008g0160a0001c0001t0012g0161a0001c0002t0009g0162others(2): Show | 5 | HG03017.hp1 HG03654.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+7328A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15259205 | ||||||
| chr1:15259602
|
G | A | 3 | a0026c0031t0003g0252a0026c0031t0003g0253a0046c0078t0007g0232 | 3 | HG02055.hp2 HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.93+7725G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15259602 | ||||||
| chr1:15259649
|
C | A | 69 | a0001c0001t0057g0250a0001c0008t0008g0204a0001c0008t0012g0205others(66): Show | 69 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.93+7772C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15259649 | ||||||
| chr1:15259706
|
C | T | 1 | a0013c0021t0002g0084 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.93+7829C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15259706 | ||||||
| chr1:15259768
|
G | A | 3 | a0003c0086t0009g0142a0004c0038t0007g0143a0012c0097t0003g0141 | 3 | HG01070.hp1 HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.93+7891G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15259768 | ||||||
| chr1:15259782
|
A | G | 257 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(254): Show | 257 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(254): Show |
intron_variant | MODIFIER | c.93+7905A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15259782 | ||||||
| chr1:15259796
|
G | A | 1 | a0032c0120t0034g0259 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.93+7919G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15259796 | ||||||
| chr1:15259910
|
C | A | 5 | a0060c0065t0043g0005a0061c0066t0040g0003a0063c0067t0039g0004others(2): Show | 5 | HG01099.hp1 HG01106.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.93+8033C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15259910 | ||||||
| chr1:15260116
|
C | T | 25 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(22): Show | 25 | HG00735.hp2 HG00738.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.93+8239C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15260116 | ||||||
| chr1:15260326
|
C | T | 1 | a0017c0017t0007g0008 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.93+8449C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15260326 | ||||||
| chr1:15260335
|
G | A | 128 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(125): Show | 128 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.93+8458G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15260335 | ||||||
| chr1:15260382
|
C | T | 94 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(91): Show | 94 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.93+8505C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15260382 | ||||||
| chr1:15260383
|
G | T | 1 | a0007c0059t0014g0167 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.93+8506G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15260383 | ||||||
| chr1:15260437
|
G | A | 3 | a0004c0004t0004g0086a0011c0034t0006g0085a0011c0099t0006g0087 | 3 | HG00558.hp1 NA18944.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.93+8560G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15260437 | ||||||
| chr1:15260502
|
G | A | 1 | a0003c0026t0001g0106 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.93+8625G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15260502 | ||||||
| chr1:15260583
|
A | G | 6 | a0001c0001t0057g0250a0002c0081t0058g0251a0007c0012t0016g0256others(3): Show | 6 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.93+8706A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15260583 | ||||||
| chr1:15260599
|
T | C | 186 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(183): Show | 186 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.93+8722T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15260599 | ||||||
| chr1:15260658
|
G | A | 20 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0012g0126others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.93+8781G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15260658 | ||||||
| chr1:15260852
|
G | C | 72 | a0001c0001t0057g0250a0001c0008t0008g0204a0001c0008t0012g0205others(69): Show | 72 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.93+8975G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15260852 | ||||||
| chr1:15260922
|
A | C | 4 | a0001c0001t0002g0081a0001c0001t0002g0093a0002c0003t0006g0083others(1): Show | 4 | HG02165.hp1 NA18955.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+9045A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15260922 | ||||||
| chr1:15261049
|
A | G | 1 | a0001c0002t0001g0080 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.93+9172A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15261049 | ||||||
| chr1:15261081
|
G | A | 4 | a0005c0005t0015g0286a0005c0070t0035g0287a0040c0077t0037g0262others(1): Show | 4 | HG02109.hp1 HG02897.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.93+9204G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15261081 | ||||||
| chr1:15261431
|
G | A | 1 | a0001c0001t0013g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.93+9554G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15261431 | ||||||
| chr1:15261684
|
T | C | 173 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(170): Show | 173 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.93+9807T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15261684 | ||||||
| chr1:15261687
|
T | C | 5 | a0001c0001t0008g0160a0001c0001t0012g0161a0001c0002t0009g0162others(2): Show | 5 | HG03017.hp1 HG03654.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+9810T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15261687 | ||||||
| chr1:15261694
|
C | T | 71 | a0001c0001t0057g0250a0001c0008t0008g0204a0001c0008t0012g0205others(68): Show | 71 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.93+9817C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15261694 | ||||||
| chr1:15261695
|
T | C | 1 | a0032c0120t0034g0259 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.93+9818T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15261695 | ||||||
| chr1:15261885
|
G | A | 7 | a0001c0001t0057g0250a0002c0081t0058g0251a0003c0098t0029g0237others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.93+10008G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15261885 | ||||||
| chr1:15261890
|
T | C | 273 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(270): Show | 273 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(270): Show |
intron_variant | MODIFIER | c.93+10013T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15261890 | ||||||
| chr1:15262000
|
C | T | 1 | a0007c0012t0016g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.93+10123C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15262000 | ||||||
| chr1:15262020
|
C | T | 23 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(20): Show | 23 | HG00735.hp2 HG00738.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.93+10143C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15262020 | ||||||
| chr1:15262211
|
A | C | 2 | a0019c0022t0018g0015a0059c0104t0045g0014 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.94-10112A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15262211 | ||||||
| chr1:15262263
|
T | C | 71 | a0001c0001t0057g0250a0001c0008t0008g0204a0001c0008t0012g0205others(68): Show | 71 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.94-10060T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15262263 | ||||||
| chr1:15262310
|
T | C | 4 | a0001c0001t0008g0160a0001c0002t0009g0162a0001c0036t0008g0163others(1): Show | 4 | HG03017.hp1 HG03654.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-10013T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15262310 | ||||||
| chr1:15262337
|
T | C | 1 | a0009c0011t0017g0294 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.94-9986T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15262337 | ||||||
| chr1:15262460
|
C | T | 3 | a0002c0080t0019g0181a0007c0012t0016g0187a0007c0082t0016g0180 | 3 | HG02896.hp1 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.94-9863C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15262460 | ||||||
| chr1:15262494
|
C | T | 23 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(20): Show | 23 | HG00735.hp2 HG00738.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.94-9829C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15262494 | ||||||
| chr1:15262669
|
A | G | 1 | a0008c0122t0009g0215 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.94-9654A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15262669 | ||||||
| chr1:15262678
|
G | A | 5 | a0005c0016t0028g0009a0010c0043t0005g0012a0010c0043t0005g0013others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-9645G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15262678 | ||||||
| chr1:15262726
|
A | G | 257 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(254): Show | 257 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(254): Show |
intron_variant | MODIFIER | c.94-9597A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15262726 | ||||||
| chr1:15262839
|
G | C | 64 | a0001c0001t0057g0250a0001c0008t0008g0204a0001c0008t0012g0205others(61): Show | 64 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.94-9484G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15262839 | ||||||
| chr1:15262904
|
A | G | 5 | a0060c0065t0043g0005a0061c0066t0040g0003a0063c0067t0039g0004others(2): Show | 5 | HG01099.hp1 HG01106.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-9419A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15262904 | ||||||
| chr1:15262952
|
G | A | 2 | a0004c0004t0004g0029a0004c0004t0004g0030 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.94-9371G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15262952 | ||||||
| chr1:15263033
|
T | G | 3 | a0004c0004t0004g0086a0011c0034t0006g0085a0011c0099t0006g0087 | 3 | HG00558.hp1 NA18944.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.94-9290T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15263033 | ||||||
| chr1:15263390
|
G | A | 46 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0008g0149others(43): Show | 46 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.94-8933G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15263390 | ||||||
| chr1:15263415
|
T | C | 1 | a0003c0037t0001g0094 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.94-8908T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15263415 | ||||||
| chr1:15263510
|
C | CT | 48 | a0001c0001t0002g0093a0001c0001t0002g0099a0001c0001t0008g0160others(45): Show | 48 | HG00621.hp1 HG00621.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.94-8788dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15263510 | |||||
| chr1:15263510
|
C | CTT | 7 | a0001c0001t0012g0161a0001c0008t0025g0113a0001c0010t0001g0182others(4): Show | 7 | HG01106.hp1 HG01261.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.94-8789_94-8788dup others(2): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15263510 | |||||
| chr1:15263510
|
CT | C | 44 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0008g0149others(41): Show | 44 | HG00609.hp1 HG01070.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.94-8788delT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15263510 | |||||
| chr1:15263510
|
CTTTTTTT others(3): Show |
C | 53 | a0001c0008t0008g0204a0001c0008t0012g0205a0001c0010t0009g0207others(50): Show | 53 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.94-8797_94-8788del others(10): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15263510 | |||||
| chr1:15263510
|
CTTTTTTT others(4): Show |
C | 2 | a0002c0007t0003g0190a0004c0057t0005g0189 | 2 | NA18964.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.94-8798_94-8788del others(11): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15263510 | |||||
| chr1:15263543
|
A | G | 1 | a0052c0088t0021g0242 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.94-8780A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15263543 | ||||||
| chr1:15263561
|
G | A | 102 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(99): Show | 102 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.94-8762G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15263561 | ||||||
| chr1:15263591
|
G | A | 1 | a0064c0063t0030g0195 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.94-8732G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15263591 | ||||||
| chr1:15263622
|
T | C | 5 | a0005c0016t0028g0009a0010c0043t0005g0012a0010c0043t0005g0013others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-8701T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15263622 | ||||||
| chr1:15263683
|
A | G | 211 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(208): Show | 211 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.94-8640A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15263683 | ||||||
| chr1:15263695
|
G | T | 5 | a0006c0014t0005g0255a0021c0117t0016g0234a0023c0130t0007g0238others(2): Show | 5 | HG00642.hp2 HG02622.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-8628G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15263695 | ||||||
| chr1:15263767
|
C | T | 2 | a0002c0003t0005g0135a0003c0006t0008g0134 | 2 | HG02602.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.94-8556C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15263767 | ||||||
| chr1:15263864
|
C | T | 2 | a0019c0022t0018g0015a0059c0104t0045g0014 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.94-8459C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15263864 | ||||||
| chr1:15263883
|
G | C | 3 | a0002c0080t0019g0181a0007c0012t0016g0187a0007c0082t0016g0180 | 3 | HG02896.hp1 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.94-8440G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15263883 | ||||||
| chr1:15264040
|
A | T | 1 | a0005c0005t0010g0279 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.94-8283A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15264040 | ||||||
| chr1:15264371
|
T | C | 3 | a0002c0080t0019g0181a0007c0012t0016g0187a0007c0082t0016g0180 | 3 | HG02896.hp1 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.94-7952T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15264371 | ||||||
| chr1:15264542
|
G | GTA | 3 | a0026c0031t0003g0252a0026c0031t0003g0253a0046c0078t0007g0232 | 3 | HG02055.hp2 HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.94-7775_94-7774dup others(2): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15264542 | |||||
| chr1:15264548
|
A | ATG | 11 | a0001c0001t0008g0160a0001c0001t0012g0161a0001c0001t0015g0267others(8): Show | 11 | HG01433.hp2 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.94-7746_94-7745dup others(2): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15264548 | |||||
| chr1:15264548
|
A | ATGTG | 15 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0012g0126others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.94-7748_94-7745dup others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15264548 | |||||
| chr1:15264548
|
A | ATGTGTG | 9 | a0001c0001t0008g0149a0001c0001t0008g0175a0002c0003t0003g0133others(6): Show | 9 | HG01952.hp2 HG02015.hp1 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.94-7750_94-7745dup others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15264548 | |||||
| chr1:15264548
|
A | ATGTGTGT others(1): Show |
4 | a0002c0003t0005g0177a0002c0003t0053g0176a0003c0009t0009g0178others(1): Show | 4 | NA18612.hp1 NA18968.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-7752_94-7745dup others(8): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15264548 | |||||
| chr1:15264548
|
A | ATGTGTGT others(3): Show |
1 | a0003c0009t0028g0191 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.94-7754_94-7745dup others(10): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15264548 | |||||
| chr1:15264548
|
A | G | 33 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(30): Show | 33 | HG00673.hp1 HG00735.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.94-7775A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15264548 | ||||||
| chr1:15264548
|
ATG | A | 51 | a0001c0001t0002g0099a0001c0002t0044g0169a0001c0008t0008g0204others(48): Show | 51 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.94-7746_94-7745del others(2): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15264548 | |||||
| chr1:15264554
|
G | A | 1 | a0017c0017t0007g0008 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.94-7769G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15264554 | ||||||
| chr1:15264578
|
G | A | 161 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(158): Show | 161 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.94-7745G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15264578 | ||||||
| chr1:15264578
|
G | GTA | 17 | a0001c0002t0018g0156a0001c0032t0014g0152a0001c0102t0012g0146others(14): Show | 17 | HG00438.hp2 HG01070.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.94-7745_94-7744ins others(2): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15264578 | ||||||
| chr1:15264578
|
G | GTGTA | 9 | a0001c0010t0001g0182a0002c0018t0007g0140a0003c0085t0055g0139others(6): Show | 9 | HG02630.hp1 HG02717.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.94-7745_94-7744ins others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15264578 | ||||||
| chr1:15264578
|
G | GTGTGTA | 22 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(19): Show | 22 | HG00673.hp1 HG00735.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.94-7745_94-7744ins others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15264578 | ||||||
| chr1:15264578
|
G | GTGTGTGT others(3): Show |
4 | a0001c0010t0001g0097a0001c0010t0001g0098a0002c0053t0020g0096others(1): Show | 4 | HG01516.hp1 HG01517.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-7745_94-7744ins others(10): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15264578 | ||||||
| chr1:15264723
|
G | A | 214 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(211): Show | 214 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.94-7600G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15264723 | ||||||
| chr1:15264794
|
T | G | 11 | a0001c0001t0008g0149a0001c0001t0008g0175a0002c0003t0003g0192others(8): Show | 11 | HG02015.hp1 HG02083.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.94-7529T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15264794 | ||||||
| chr1:15265072
|
G | T | 1 | a0004c0004t0004g0073 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.94-7251G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15265072 | ||||||
| chr1:15265075
|
A | G | 35 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(32): Show | 35 | HG00673.hp1 HG00735.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.94-7248A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15265075 | ||||||
| chr1:15265145
|
T | C | 35 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(32): Show | 35 | HG00673.hp1 HG00735.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.94-7178T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15265145 | ||||||
| chr1:15265171
|
G | T | 1 | a0002c0134t0003g0209 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.94-7152G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15265171 | ||||||
| chr1:15265433
|
T | C | 214 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(211): Show | 214 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.94-6890T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15265433 | ||||||
| chr1:15265526
|
G | A | 5 | a0001c0001t0008g0160a0001c0001t0012g0161a0001c0002t0009g0162others(2): Show | 5 | HG03017.hp1 HG03654.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-6797G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15265526 | ||||||
| chr1:15265607
|
C | T | 9 | a0001c0001t0008g0175a0002c0003t0003g0192a0002c0003t0005g0172others(6): Show | 9 | HG02083.hp2 HG02523.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.94-6716C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15265607 | ||||||
| chr1:15265764
|
G | C | 32 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0008g0160others(29): Show | 32 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.94-6559G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15265764 | ||||||
| chr1:15265970
|
C | CA | 24 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.94-6334dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15265970 | |||||
| chr1:15265970
|
C | CAA | 7 | a0002c0003t0006g0083a0002c0018t0021g0247a0002c0035t0006g0031others(4): Show | 7 | HG01099.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-6335_94-6334dup others(2): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15265970 | |||||
| chr1:15265970
|
C | CAAA | 159 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(156): Show | 159 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.94-6336_94-6334dup others(3): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15265970 | |||||
| chr1:15265970
|
C | CAAAA | 18 | a0001c0002t0031g0088a0002c0007t0005g0212a0002c0018t0007g0140others(15): Show | 18 | HG01070.hp1 HG01884.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.94-6337_94-6334dup others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15265970 | |||||
| chr1:15265970
|
CA | C | 12 | a0001c0001t0008g0149a0001c0001t0008g0175a0002c0003t0003g0192others(9): Show | 12 | HG01070.hp2 HG01071.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.94-6334delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15265970 | |||||
| chr1:15265988
|
A | AG | 25 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0008g0160others(22): Show | 25 | HG01069.hp1 HG01071.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.94-6335_94-6334ins others(1): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15265988 | ||||||
| chr1:15265990
|
G | A | 1 | a0007c0033t0007g0138 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.94-6333G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15265990 | ||||||
| chr1:15265992
|
G | A | 1 | a0007c0033t0007g0138 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.94-6331G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15265992 | ||||||
| chr1:15266016
|
G | A | 3 | a0001c0001t0002g0099a0001c0002t0044g0169a0001c0092t0002g0100 | 3 | HG03834.hp2 NA19056.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.94-6307G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15266016 | ||||||
| chr1:15266140
|
C | T | 94 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(91): Show | 94 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.94-6183C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15266140 | ||||||
| chr1:15266320
|
G | A | 3 | a0002c0080t0019g0181a0007c0012t0016g0187a0007c0082t0016g0180 | 3 | HG02896.hp1 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.94-6003G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15266320 | ||||||
| chr1:15266409
|
C | CT | 17 | a0001c0001t0013g0104a0001c0002t0001g0079a0001c0002t0018g0156others(14): Show | 17 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.94-5900dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15266409 | |||||
| chr1:15266409
|
CT | C | 8 | a0001c0108t0001g0165a0004c0004t0007g0001a0004c0004t0007g0002others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.94-5900delT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15266409 | |||||
| chr1:15266493
|
C | G | 4 | a0001c0001t0015g0267a0001c0013t0011g0266a0005c0030t0010g0264others(1): Show | 4 | HG01433.hp2 HG02698.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-5830C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15266493 | ||||||
| chr1:15266555
|
A | G | 2 | a0006c0014t0005g0255a0023c0130t0007g0238 | 2 | HG00642.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.94-5768A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15266555 | ||||||
| chr1:15266617
|
T | C | 1 | a0032c0120t0034g0259 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.94-5706T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15266617 | ||||||
| chr1:15266641
|
A | G | 24 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.94-5682A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15266641 | ||||||
| chr1:15266752
|
C | T | 1 | a0049c0052t0004g0120 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.94-5571C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15266752 | ||||||
| chr1:15266803
|
C | A | 10 | a0002c0018t0021g0247a0002c0019t0027g0244a0007c0012t0026g0245others(7): Show | 10 | HG02572.hp2 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.94-5520C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15266803 | ||||||
| chr1:15266836
|
A | G | 6 | a0060c0065t0043g0005a0061c0066t0040g0003a0063c0067t0039g0004others(3): Show | 6 | HG01099.hp1 HG01106.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.94-5487A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15266836 | ||||||
| chr1:15266877
|
A | G | 206 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(203): Show | 206 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.94-5446A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15266877 | ||||||
| chr1:15267000
|
GTT | G | 206 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(203): Show | 206 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.94-5319_94-5318del others(2): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15267000 | |||||
| chr1:15267061
|
T | A | 260 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(257): Show | 260 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(257): Show |
intron_variant | MODIFIER | c.94-5262T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15267061 | ||||||
| chr1:15267156
|
G | A | 4 | a0002c0003t0005g0177a0002c0003t0053g0176a0003c0009t0009g0178others(1): Show | 4 | NA18968.hp1 NA18970.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-5167G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15267156 | ||||||
| chr1:15267170
|
C | T | 94 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(91): Show | 94 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.94-5153C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15267170 | ||||||
| chr1:15267224
|
T | C | 10 | a0001c0001t0008g0160a0001c0001t0012g0161a0001c0002t0009g0162others(7): Show | 10 | HG01069.hp1 HG01071.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.94-5099T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15267224 | ||||||
| chr1:15267321
|
T | C | 1 | a0031c0119t0009g0257 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.94-5002T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15267321 | ||||||
| chr1:15267470
|
A | G | 103 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(100): Show | 103 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.94-4853A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15267470 | ||||||
| chr1:15267536
|
C | T | 11 | a0001c0001t0008g0149a0001c0001t0008g0175a0002c0003t0003g0192others(8): Show | 11 | HG02015.hp1 HG02083.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.94-4787C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15267536 | ||||||
| chr1:15267549
|
C | T | 260 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(257): Show | 260 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(257): Show |
intron_variant | MODIFIER | c.94-4774C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15267549 | ||||||
| chr1:15267584
|
GTGCTTTC others(6): Show |
G | 1 | a0003c0098t0029g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.94-4738_94-4726del others(13): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15267584 | ||||||
| chr1:15267701
|
G | A | 39 | a0001c0008t0008g0204a0001c0008t0012g0205a0001c0010t0009g0207others(36): Show | 39 | HG00438.hp1 HG00544.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.94-4622G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15267701 | ||||||
| chr1:15267783
|
AAAT | A | 24 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.94-4532_94-4530del others(3): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15267783 | |||||
| chr1:15267945
|
TA | T | 137 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(134): Show | 137 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.94-4372delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15267945 | |||||
| chr1:15267950
|
A | AT | 69 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(66): Show | 69 | HG00642.hp2 HG00673.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.94-4373_94-4372ins others(1): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15267950 | ||||||
| chr1:15267950
|
A | T | 7 | a0001c0001t0057g0250a0002c0081t0058g0251a0003c0098t0029g0237others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.94-4373A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15267950 | ||||||
| chr1:15268179
|
T | A | 24 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.94-4144T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15268179 | ||||||
| chr1:15268187
|
T | A | 1 | a0008c0125t0012g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.94-4136T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15268187 | ||||||
| chr1:15268482
|
G | A | 94 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(91): Show | 94 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.94-3841G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15268482 | ||||||
| chr1:15268483
|
C | T | 206 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(203): Show | 206 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.94-3840C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15268483 | ||||||
| chr1:15268566
|
G | A | 121 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(118): Show | 121 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.94-3757G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15268566 | ||||||
| chr1:15268822
|
T | C | 25 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0008g0160others(22): Show | 25 | HG01069.hp1 HG01071.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.94-3501T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15268822 | ||||||
| chr1:15268963
|
T | C | 19 | a0001c0001t0008g0149a0001c0001t0008g0175a0002c0003t0003g0192others(16): Show | 19 | HG01070.hp1 HG01884.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.94-3360T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15268963 | ||||||
| chr1:15269001
|
C | G | 1 | a0003c0098t0029g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.94-3322C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15269001 | ||||||
| chr1:15269038
|
A | C | 55 | a0001c0008t0008g0204a0001c0008t0012g0205a0001c0010t0009g0207others(52): Show | 55 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.94-3285A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15269038 | ||||||
| chr1:15269063
|
T | C | 1 | a0002c0003t0014g0151 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.94-3260T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15269063 | ||||||
| chr1:15269101
|
A | G | 2 | a0001c0001t0013g0072a0001c0001t0013g0092 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.94-3222A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15269101 | ||||||
| chr1:15269180
|
A | T | 204 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(201): Show | 204 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.94-3143A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15269180 | ||||||
| chr1:15269188
|
C | G | 1 | a0002c0003t0003g0133 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.94-3135C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15269188 | ||||||
| chr1:15269269
|
ATCTT | A | 7 | a0001c0001t0057g0250a0002c0081t0058g0251a0003c0098t0029g0237others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.94-3049_94-3046del others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15269269 | |||||
| chr1:15269684
|
C | T | 206 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(203): Show | 206 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.94-2639C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15269684 | ||||||
| chr1:15269790
|
G | A | 206 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(203): Show | 206 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.94-2533G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15269790 | ||||||
| chr1:15269852
|
A | T | 1 | a0039c0126t0019g0185 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.94-2471A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15269852 | ||||||
| chr1:15269906
|
T | G | 1 | a0009c0028t0020g0159 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.94-2417T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15269906 | ||||||
| chr1:15269915
|
C | CT | 12 | a0001c0001t0012g0161a0002c0003t0003g0192a0005c0005t0010g0274others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.94-2390dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15269915 | |||||
| chr1:15269915
|
C | CTT | 51 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0012g0126others(48): Show | 51 | HG00673.hp1 HG00735.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.94-2391_94-2390dup others(2): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15269915 | |||||
| chr1:15269915
|
CT | C | 116 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(113): Show | 116 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.94-2390delT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15269915 | |||||
| chr1:15270013
|
T | C | 206 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(203): Show | 206 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.94-2310T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15270013 | ||||||
| chr1:15270033
|
A | C | 228 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(225): Show | 228 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(225): Show |
intron_variant | MODIFIER | c.94-2290A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15270033 | ||||||
| chr1:15270144
|
C | A | 104 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(101): Show | 104 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.94-2179C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15270144 | ||||||
| chr1:15270149
|
G | A | 104 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(101): Show | 104 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.94-2174G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15270149 | ||||||
| chr1:15270150
|
A | T | 104 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(101): Show | 104 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.94-2173A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15270150 | ||||||
| chr1:15270203
|
A | G | 206 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(203): Show | 206 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.94-2120A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15270203 | ||||||
| chr1:15270216
|
C | T | 44 | a0001c0008t0008g0204a0001c0008t0012g0205a0001c0010t0009g0207others(41): Show | 44 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.94-2107C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15270216 | ||||||
| chr1:15270403
|
G | A | 1 | a0012c0051t0011g0284 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.94-1920G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15270403 | ||||||
| chr1:15270473
|
T | C | 11 | a0001c0001t0008g0149a0001c0001t0008g0175a0002c0003t0003g0192others(8): Show | 11 | HG02015.hp1 HG02083.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.94-1850T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15270473 | ||||||
| chr1:15270838
|
G | GA | 105 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(102): Show | 105 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.94-1484dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15270838 | |||||
| chr1:15270996
|
A | G | 9 | a0001c0002t0018g0156a0001c0032t0014g0152a0001c0090t0048g0158others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.94-1327A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15270996 | ||||||
| chr1:15271018
|
A | G | 1 | a0005c0070t0035g0287 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.94-1305A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271018 | ||||||
| chr1:15271078
|
G | A | 2 | a0042c0069t0023g0293a0043c0068t0011g0292 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.94-1245G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271078 | ||||||
| chr1:15271118
|
A | G | 206 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(203): Show | 206 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.94-1205A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271118 | ||||||
| chr1:15271138
|
C | CA | 16 | a0001c0001t0002g0070a0001c0001t0002g0093a0001c0001t0002g0099others(13): Show | 16 | HG00609.hp2 HG00673.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.94-1185_94-1184ins others(1): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271138 | ||||||
| chr1:15271138
|
CGGA | C | 22 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(19): Show | 22 | HG00735.hp2 HG00738.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.94-1184_94-1182del others(3): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271138 | ||||||
| chr1:15271138
|
CGGAAA | C | 17 | a0001c0090t0048g0158a0002c0018t0021g0247a0002c0019t0027g0244others(14): Show | 17 | HG01099.hp1 HG01106.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.94-1184_94-1180del others(5): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271138 | ||||||
| chr1:15271138
|
CGGAAAA | C | 4 | a0002c0035t0006g0026a0004c0038t0014g0155a0012c0079t0027g0248others(1): Show | 4 | HG02723.hp2 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-1184_94-1179del others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271138 | ||||||
| chr1:15271139
|
G | A | 145 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(142): Show | 145 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.94-1184G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271139 | ||||||
| chr1:15271140
|
G | A | 16 | a0001c0001t0002g0070a0001c0001t0002g0093a0001c0001t0002g0099others(13): Show | 16 | HG00609.hp2 HG00673.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.94-1183G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271140 | ||||||
| chr1:15271140
|
G | GA | 15 | a0001c0001t0008g0160a0001c0036t0008g0163a0004c0004t0005g0164others(12): Show | 15 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.94-1160dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15271140 | |||||
| chr1:15271140
|
G | GAA | 92 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(89): Show | 92 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.94-1161_94-1160dup others(2): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15271140 | |||||
| chr1:15271140
|
G | GAAA | 51 | a0001c0002t0001g0025a0001c0002t0001g0079a0001c0002t0001g0102others(48): Show | 51 | HG00438.hp1 HG00544.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.94-1162_94-1160dup others(3): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15271140 | |||||
| chr1:15271140
|
G | GAAAA | 7 | a0001c0008t0008g0204a0002c0007t0005g0212a0003c0055t0012g0213others(4): Show | 7 | HG02056.hp2 NA18943.hp1 NA18991.hp1 others(4): Show |
intron_variant | MODIFIER | c.94-1163_94-1160dup others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15271140 | |||||
| chr1:15271140
|
GA | G | 32 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0008g0149others(29): Show | 32 | HG01070.hp1 HG01192.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.94-1160delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15271140 | |||||
| chr1:15271142
|
A | G | 1 | a0003c0026t0001g0106 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.94-1181A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271142 | ||||||
| chr1:15271143
|
A | G | 22 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(19): Show | 22 | HG00735.hp2 HG00738.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.94-1180A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271143 | ||||||
| chr1:15271145
|
A | G | 17 | a0001c0090t0048g0158a0002c0018t0021g0247a0002c0019t0027g0244others(14): Show | 17 | HG01099.hp1 HG01106.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.94-1178A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271145 | ||||||
| chr1:15271146
|
A | G | 4 | a0002c0035t0006g0026a0004c0038t0014g0155a0012c0079t0027g0248others(1): Show | 4 | HG02723.hp2 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-1177A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271146 | ||||||
| chr1:15271147
|
A | G | 1 | a0032c0120t0034g0259 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.94-1176A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271147 | ||||||
| chr1:15271176
|
G | A | 206 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(203): Show | 206 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.94-1147G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271176 | ||||||
| chr1:15271179
|
A | G | 293 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(290): Show | 293 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(290): Show |
intron_variant | MODIFIER | c.94-1144A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271179 | ||||||
| chr1:15271185
|
T | C | 206 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(203): Show | 206 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.94-1138T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271185 | ||||||
| chr1:15271206
|
G | C | 206 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(203): Show | 206 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.94-1117G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271206 | ||||||
| chr1:15271262
|
G | A | 206 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(203): Show | 206 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.94-1061G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271262 | ||||||
| chr1:15271295
|
G | A | 24 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(21): Show | 24 | HG00735.hp2 HG00738.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.94-1028G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271295 | ||||||
| chr1:15271530
|
A | G | 39 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(36): Show | 39 | HG00735.hp2 HG00738.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.94-793A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271530 | ||||||
| chr1:15271620
|
C | CGCATGGG others(12): Show |
206 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(203): Show | 206 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.94-691_94-690insAC others(17): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr1 | 15271620 | |||||
| chr1:15271620
|
C | T | 4 | a0015c0023t0008g0123a0015c0023t0008g0130a0015c0023t0008g0131others(1): Show | 4 | HG02132.hp2 NA18960.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-703C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271620 | ||||||
| chr1:15271643
|
A | G | 6 | a0001c0001t0057g0250a0002c0081t0058g0251a0007c0012t0016g0256others(3): Show | 6 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.94-680A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271643 | ||||||
| chr1:15271768
|
C | T | 7 | a0002c0019t0027g0244a0016c0040t0021g0249a0018c0020t0022g0239others(4): Show | 7 | HG02572.hp2 HG02615.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-555C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271768 | ||||||
| chr1:15271857
|
C | T | 1 | a0002c0007t0005g0212 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.94-466C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271857 | ||||||
| chr1:15271916
|
A | G | 1 | a0003c0006t0002g0103 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.94-407A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271916 | ||||||
| chr1:15271939
|
C | T | 1 | a0017c0017t0007g0008 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.94-384C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271939 | ||||||
| chr1:15271984
|
G | C | 1 | a0062c0062t0011g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.94-339G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15271984 | ||||||
| chr1:15272241
|
A | C | 11 | a0001c0001t0008g0149a0001c0001t0008g0175a0002c0003t0003g0192others(8): Show | 11 | HG02015.hp1 HG02083.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.94-82A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15272241 | ||||||
| chr1:15272316
|
G | A | 4 | a0001c0001t0013g0104a0001c0002t0049g0101a0007c0033t0014g0068others(1): Show | 4 | HG02145.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.94-7G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 2/33 | chr1 | 15272316 | ||||||
| chr1:15272573
|
G | A | 47 | a0001c0008t0002g0095a0001c0008t0008g0204a0001c0008t0012g0205others(44): Show | 47 | HG00438.hp1 HG00544.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.300+44G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15272573 | ||||||
| chr1:15272608
|
C | T | 1 | a0003c0006t0008g0134 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.300+79C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15272608 | ||||||
| chr1:15272664
|
G | T | 219 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(216): Show | 219 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(216): Show |
intron_variant | MODIFIER | c.300+135G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15272664 | ||||||
| chr1:15272668
|
G | C | 219 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(216): Show | 219 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(216): Show |
intron_variant | MODIFIER | c.300+139G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15272668 | ||||||
| chr1:15272787
|
T | C | 11 | a0001c0001t0008g0149a0001c0001t0008g0175a0002c0003t0003g0192others(8): Show | 11 | HG02015.hp1 HG02083.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.300+258T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15272787 | ||||||
| chr1:15272869
|
A | G | 219 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(216): Show | 219 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(216): Show |
intron_variant | MODIFIER | c.300+340A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15272869 | ||||||
| chr1:15273129
|
G | A | 49 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0008g0160others(46): Show | 49 | HG00673.hp1 HG01069.hp1 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.300+600G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15273129 | ||||||
| chr1:15273296
|
A | G | 8 | a0001c0008t0008g0204a0001c0010t0009g0207a0002c0007t0003g0186others(5): Show | 8 | HG00544.hp1 HG02056.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.300+767A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15273296 | ||||||
| chr1:15273473
|
G | A | 1 | a0006c0014t0005g0255 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.300+944G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15273473 | ||||||
| chr1:15273486
|
C | CT | 198 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(195): Show | 198 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.300+959dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15273486 | |||||
| chr1:15273553
|
T | C | 209 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(206): Show | 209 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.300+1024T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15273553 | ||||||
| chr1:15273589
|
A | G | 195 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(192): Show | 195 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.300+1060A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15273589 | ||||||
| chr1:15273671
|
T | G | 198 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(195): Show | 198 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.300+1142T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15273671 | ||||||
| chr1:15273681
|
G | T | 1 | a0019c0022t0018g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.300+1152G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15273681 | ||||||
| chr1:15273721
|
C | T | 247 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(244): Show | 247 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.300+1192C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15273721 | ||||||
| chr1:15273791
|
G | A | 4 | a0001c0001t0002g0081a0001c0001t0002g0093a0002c0003t0006g0083others(1): Show | 4 | HG02165.hp1 NA18955.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+1262G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15273791 | ||||||
| chr1:15273823
|
C | T | 10 | a0001c0002t0001g0061a0001c0002t0001g0063a0001c0002t0001g0065others(7): Show | 10 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.300+1294C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15273823 | ||||||
| chr1:15273907
|
A | C | 209 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(206): Show | 209 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.300+1378A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15273907 | ||||||
| chr1:15274057
|
T | C | 34 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(31): Show | 34 | HG00673.hp1 HG00735.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.300+1528T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15274057 | ||||||
| chr1:15274153
|
C | T | 33 | a0001c0001t0008g0149a0001c0001t0008g0175a0001c0001t0013g0104others(30): Show | 33 | HG02015.hp1 HG02055.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.300+1624C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15274153 | ||||||
| chr1:15274157
|
G | A | 3 | a0003c0006t0002g0018a0004c0004t0004g0027a0011c0034t0006g0034 | 3 | HG00544.hp2 NA18994.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.300+1628G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15274157 | ||||||
| chr1:15274303
|
T | C | 137 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(134): Show | 137 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.300+1774T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15274303 | ||||||
| chr1:15274374
|
G | T | 2 | a0017c0017t0007g0147a0017c0017t0007g0148 | 2 | HG02486.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.300+1845G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15274374 | ||||||
| chr1:15274438
|
T | C | 7 | a0001c0001t0057g0250a0002c0081t0058g0251a0003c0098t0029g0237others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.300+1909T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15274438 | ||||||
| chr1:15274452
|
C | CA | 8 | a0001c0002t0001g0102a0052c0088t0021g0242a0060c0065t0043g0005others(5): Show | 8 | HG01099.hp1 HG01106.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.300+1933dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15274452 | |||||
| chr1:15274599
|
A | G | 209 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(206): Show | 209 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.300+2070A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15274599 | ||||||
| chr1:15274611
|
CA | C | 247 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(244): Show | 247 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.300+2095delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15274611 | |||||
| chr1:15274674
|
A | T | 3 | a0002c0080t0019g0181a0007c0012t0016g0187a0007c0082t0016g0180 | 3 | HG02896.hp1 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.300+2145A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15274674 | ||||||
| chr1:15274772
|
G | A | 11 | a0001c0001t0008g0149a0001c0001t0008g0175a0002c0003t0003g0192others(8): Show | 11 | HG02015.hp1 HG02083.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.300+2243G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15274772 | ||||||
| chr1:15274968
|
C | CT | 6 | a0014c0112t0007g0202a0014c0118t0007g0198a0020c0116t0052g0200others(3): Show | 6 | HG01167.hp1 HG01243.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.300+2451dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15274968 | |||||
| chr1:15275097
|
G | A | 4 | a0002c0003t0005g0177a0002c0003t0053g0176a0003c0009t0009g0178others(1): Show | 4 | NA18968.hp1 NA18970.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+2568G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15275097 | ||||||
| chr1:15275112
|
A | G | 34 | a0001c0008t0002g0095a0001c0008t0025g0112a0001c0008t0025g0113others(31): Show | 34 | HG00673.hp1 HG00735.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.300+2583A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15275112 | ||||||
| chr1:15275205
|
G | A | 1 | a0005c0005t0010g0279 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.300+2676G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15275205 | ||||||
| chr1:15275239
|
G | A | 63 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0008g0160others(60): Show | 63 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.300+2710G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15275239 | ||||||
| chr1:15275508
|
C | T | 3 | a0001c0002t0018g0156a0004c0038t0014g0155a0054c0084t0047g0154 | 3 | HG02109.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.300+2979C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15275508 | ||||||
| chr1:15275703
|
C | T | 2 | a0001c0008t0025g0112a0001c0008t0025g0113 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.300+3174C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15275703 | ||||||
| chr1:15275767
|
G | C | 12 | a0001c0001t0008g0149a0001c0001t0008g0175a0002c0003t0003g0192others(9): Show | 12 | HG02015.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.300+3238G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15275767 | ||||||
| chr1:15275834
|
C | T | 111 | a0001c0001t0008g0149a0001c0001t0008g0175a0001c0001t0013g0072others(108): Show | 111 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(108): Show |
intron_variant | MODIFIER | c.300+3305C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15275834 | ||||||
| chr1:15275837
|
T | C | 3 | a0001c0002t0001g0038a0001c0039t0001g0036a0001c0039t0001g0037 | 3 | HG03017.hp2 HG03491.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.300+3308T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15275837 | ||||||
| chr1:15276256
|
T | C | 119 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0008g0149others(116): Show | 119 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.300+3727T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15276256 | ||||||
| chr1:15276914
|
C | T | 1 | a0020c0111t0030g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.300+4385C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15276914 | ||||||
| chr1:15276934
|
TG | T | 81 | a0001c0001t0002g0049a0001c0001t0002g0054a0001c0001t0002g0057others(78): Show | 81 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.300+4406delG | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15276934 | ||||||
| chr1:15277007
|
C | T | 7 | a0001c0002t0018g0156a0001c0032t0014g0152a0001c0102t0012g0146others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.300+4478C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15277007 | ||||||
| chr1:15277159
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.300+4630C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15277159 | ||||||
| chr1:15277189
|
C | T | 1 | a0004c0096t0002g0033 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.300+4660C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15277189 | ||||||
| chr1:15277246
|
C | T | 2 | a0001c0001t0002g0057a0001c0002t0001g0058 | 2 | NA18960.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.300+4717C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15277246 | ||||||
| chr1:15277372
|
C | T | 3 | a0002c0080t0019g0181a0007c0012t0016g0187a0007c0082t0016g0180 | 3 | HG02896.hp1 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.300+4843C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15277372 | ||||||
| chr1:15277401
|
C | T | 5 | a0005c0016t0028g0009a0010c0043t0005g0012a0010c0043t0005g0013others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+4872C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15277401 | ||||||
| chr1:15277447
|
T | C | 5 | a0005c0016t0028g0009a0010c0043t0005g0012a0010c0043t0005g0013others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+4918T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15277447 | ||||||
| chr1:15277499
|
G | A | 1 | a0021c0113t0016g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.300+4970G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15277499 | ||||||
| chr1:15277806
|
A | G | 9 | a0002c0018t0007g0140a0003c0085t0055g0139a0003c0086t0009g0142others(6): Show | 9 | HG01070.hp1 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+5277A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15277806 | ||||||
| chr1:15277830
|
T | C | 1 | a0012c0079t0027g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.300+5301T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15277830 | ||||||
| chr1:15277847
|
G | A | 1 | a0017c0017t0007g0008 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.300+5318G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15277847 | ||||||
| chr1:15278000
|
C | T | 12 | a0001c0001t0008g0149a0006c0014t0003g0224a0006c0014t0005g0220others(9): Show | 12 | HG02015.hp1 HG02056.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.300+5471C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15278000 | ||||||
| chr1:15278063
|
C | T | 3 | a0003c0006t0002g0018a0004c0004t0004g0027a0011c0034t0006g0034 | 3 | HG00544.hp2 NA18994.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.300+5534C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15278063 | ||||||
| chr1:15278064
|
A | G | 105 | a0001c0001t0002g0049a0001c0001t0002g0054a0001c0001t0002g0057others(102): Show | 105 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.300+5535A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15278064 | ||||||
| chr1:15278083
|
G | A | 20 | a0001c0001t0008g0149a0003c0086t0009g0142a0004c0038t0007g0143others(17): Show | 20 | HG00642.hp2 HG01070.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.300+5554G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15278083 | ||||||
| chr1:15278097
|
C | A | 25 | a0002c0003t0003g0192a0002c0003t0005g0172a0002c0003t0005g0177others(22): Show | 25 | HG00642.hp2 HG01243.hp2 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.300+5568C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15278097 | ||||||
| chr1:15278170
|
T | TTTGC | 135 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0008g0149others(132): Show | 135 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(132): Show |
intron_variant | MODIFIER | c.300+5643_300+5644i others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15278170 | |||||
| chr1:15278265
|
C | T | 1 | a0008c0132t0060g0229 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.300+5736C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15278265 | ||||||
| chr1:15278332
|
A | C | 1 | a0008c0132t0060g0229 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.300+5803A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15278332 | ||||||
| chr1:15278377
|
C | T | 2 | a0004c0004t0004g0029a0004c0004t0004g0030 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.300+5848C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15278377 | ||||||
| chr1:15278378
|
C | T | 10 | a0001c0001t0013g0104a0001c0002t0049g0101a0002c0035t0006g0026others(7): Show | 10 | HG02145.hp2 HG02615.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.300+5849C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15278378 | ||||||
| chr1:15278390
|
T | C | 1 | a0003c0006t0008g0134 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.300+5861T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15278390 | ||||||
| chr1:15278452
|
G | A | 1 | a0013c0060t0001g0166 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.300+5923G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15278452 | ||||||
| chr1:15278475
|
C | CT | 54 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0008g0149others(51): Show | 54 | HG00673.hp1 HG00673.hp2 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.300+5962dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15278475 | |||||
| chr1:15278475
|
C | CTTT | 14 | a0001c0001t0008g0175a0001c0002t0018g0156a0002c0003t0003g0192others(11): Show | 14 | HG02040.hp2 HG02083.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.300+5960_300+5962d others(5): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15278475 | |||||
| chr1:15278475
|
C | CTTTTTTT others(3): Show |
14 | a0001c0001t0002g0040a0001c0001t0013g0072a0001c0001t0013g0092others(11): Show | 14 | HG00438.hp1 HG01256.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.300+5953_300+5962d others(12): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15278475 | |||||
| chr1:15278475
|
C | CTTTTTTT others(4): Show |
35 | a0001c0001t0002g0041a0001c0001t0010g0281a0001c0001t0015g0267others(32): Show | 35 | HG00558.hp2 HG00735.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.300+5952_300+5962d others(13): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15278475 | |||||
| chr1:15278475
|
C | CTTTTTTT others(5): Show |
10 | a0001c0008t0002g0095a0001c0010t0009g0207a0001c0015t0001g0111others(7): Show | 10 | HG01928.hp1 HG02135.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.300+5951_300+5962d others(14): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15278475 | |||||
| chr1:15278475
|
C | CTTTTTTT others(6): Show |
17 | a0001c0001t0013g0104a0001c0002t0049g0101a0001c0032t0014g0152others(14): Show | 17 | HG01167.hp1 HG01243.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.300+5950_300+5962d others(15): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15278475 | |||||
| chr1:15278475
|
C | CTTTTTTT others(7): Show |
4 | a0001c0102t0012g0146a0002c0018t0018g0153a0007c0012t0016g0256others(1): Show | 4 | HG02257.hp2 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+5949_300+5962d others(16): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15278475 | |||||
| chr1:15278475
|
C | CTTTTTTT others(8): Show |
1 | a0014c0110t0008g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.300+5948_300+5962d others(17): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15278475 | |||||
| chr1:15278475
|
C | CTTTTTTT others(9): Show |
1 | a0002c0003t0006g0157 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.300+5947_300+5962d others(18): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15278475 | |||||
| chr1:15278475
|
C | CTTTTTTT others(10): Show |
1 | a0001c0090t0048g0158 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.300+5962_300+5963i others(19): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15278475 | |||||
| chr1:15278521
|
T | C | 3 | a0001c0010t0001g0097a0001c0010t0001g0098a0002c0053t0020g0096 | 3 | HG01516.hp1 HG01517.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.300+5992T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15278521 | ||||||
| chr1:15278752
|
G | A | 2 | a0004c0004t0007g0001a0004c0004t0007g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.300+6223G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15278752 | ||||||
| chr1:15278926
|
C | A | 7 | a0001c0002t0018g0156a0001c0032t0014g0152a0001c0102t0012g0146others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.300+6397C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15278926 | ||||||
| chr1:15278943
|
T | C | 101 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0008g0149others(98): Show | 101 | HG00642.hp2 HG00673.hp1 HG00673.hp2 others(98): Show |
intron_variant | MODIFIER | c.300+6414T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15278943 | ||||||
| chr1:15278972
|
G | T | 101 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0008g0149others(98): Show | 101 | HG00642.hp2 HG00673.hp1 HG00673.hp2 others(98): Show |
intron_variant | MODIFIER | c.300+6443G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15278972 | ||||||
| chr1:15279135
|
G | A | 4 | a0001c0001t0013g0104a0001c0002t0049g0101a0007c0033t0014g0068others(1): Show | 4 | HG02145.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+6606G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15279135 | ||||||
| chr1:15279406
|
G | T | 133 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(130): Show | 133 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.300+6877G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15279406 | ||||||
| chr1:15279463
|
GC | G | 243 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(240): Show | 243 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(240): Show |
intron_variant | MODIFIER | c.300+6941delC | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15279463 | |||||
| chr1:15279554
|
C | CA | 82 | a0001c0001t0002g0049a0001c0001t0002g0054a0001c0001t0002g0081others(79): Show | 82 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.300+7045dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15279554 | |||||
| chr1:15279554
|
C | CAA | 79 | a0001c0001t0002g0041a0001c0001t0002g0057a0001c0001t0002g0070others(76): Show | 79 | HG00438.hp1 HG00558.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.300+7044_300+7045d others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15279554 | |||||
| chr1:15279554
|
C | CAAA | 7 | a0001c0001t0002g0040a0002c0019t0004g0118a0006c0014t0003g0214others(4): Show | 7 | HG02071.hp2 HG02145.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.300+7043_300+7045d others(5): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15279554 | |||||
| chr1:15279554
|
CAA | C | 10 | a0023c0130t0007g0238a0037c0128t0007g0233a0038c0129t0007g0235others(7): Show | 10 | HG01099.hp1 HG01106.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.300+7044_300+7045d others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15279554 | |||||
| chr1:15279554
|
CAAA | C | 32 | a0001c0001t0008g0175a0001c0001t0013g0104a0001c0002t0018g0156others(29): Show | 32 | HG02040.hp2 HG02055.hp1 HG02083.hp2 others(29): Show |
intron_variant | MODIFIER | c.300+7043_300+7045d others(5): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15279554 | |||||
| chr1:15279554
|
CAAAA | C | 9 | a0001c0001t0057g0250a0002c0019t0027g0244a0002c0081t0058g0251others(6): Show | 9 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+7042_300+7045d others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15279554 | |||||
| chr1:15279633
|
A | G | 1 | a0007c0012t0016g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.300+7104A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15279633 | ||||||
| chr1:15279788
|
G | T | 51 | a0001c0001t0008g0175a0001c0001t0013g0104a0001c0001t0057g0250others(48): Show | 51 | HG01099.hp1 HG01106.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.300+7259G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15279788 | ||||||
| chr1:15279957
|
C | T | 137 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(134): Show | 137 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.300+7428C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15279957 | ||||||
| chr1:15280227
|
T | C | 101 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0008g0149others(98): Show | 101 | HG00642.hp2 HG00673.hp1 HG00673.hp2 others(98): Show |
intron_variant | MODIFIER | c.300+7698T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15280227 | ||||||
| chr1:15280574
|
G | A | 51 | a0001c0001t0008g0175a0001c0001t0013g0104a0001c0001t0057g0250others(48): Show | 51 | HG01099.hp1 HG01106.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.300+8045G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15280574 | ||||||
| chr1:15280580
|
C | G | 1 | a0002c0080t0019g0181 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.300+8051C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15280580 | ||||||
| chr1:15280704
|
A | G | 11 | a0001c0001t0057g0250a0002c0019t0027g0244a0002c0080t0019g0181others(8): Show | 11 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.300+8175A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15280704 | ||||||
| chr1:15280750
|
G | A | 1 | a0003c0098t0029g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.300+8221G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15280750 | ||||||
| chr1:15280778
|
C | T | 13 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0012g0126others(10): Show | 13 | HG01192.hp2 HG01255.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.300+8249C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15280778 | ||||||
| chr1:15280808
|
G | A | 51 | a0001c0032t0023g0282a0005c0005t0010g0274a0005c0005t0010g0277others(48): Show | 51 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.300+8279G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15280808 | ||||||
| chr1:15280810
|
C | T | 2 | a0010c0043t0005g0012a0010c0043t0005g0013 | 2 | HG01261.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.300+8281C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15280810 | ||||||
| chr1:15280853
|
C | G | 5 | a0006c0024t0003g0226a0006c0024t0003g0231a0006c0024t0005g0227others(2): Show | 5 | HG00673.hp1 NA18984.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+8324C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15280853 | ||||||
| chr1:15280917
|
C | T | 1 | a0001c0002t0018g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.300+8388C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15280917 | ||||||
| chr1:15281271
|
T | G | 1 | a0006c0045t0003g0225 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.301-8128T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15281271 | ||||||
| chr1:15281391
|
G | A | 1 | a0016c0107t0003g0145 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.301-8008G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15281391 | ||||||
| chr1:15281430
|
A | G | 1 | a0004c0004t0004g0116 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.301-7969A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15281430 | ||||||
| chr1:15281685
|
C | A | 1 | a0005c0070t0035g0287 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.301-7714C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15281685 | ||||||
| chr1:15281693
|
G | A | 1 | a0001c0008t0008g0204 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.301-7706G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15281693 | ||||||
| chr1:15281721
|
A | G | 3 | a0001c0001t0002g0070a0001c0036t0002g0055a0003c0037t0001g0094 | 3 | HG01256.hp1 HG01928.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.301-7678A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15281721 | ||||||
| chr1:15281728
|
T | G | 51 | a0001c0032t0023g0282a0005c0005t0010g0274a0005c0005t0010g0277others(48): Show | 51 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.301-7671T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15281728 | ||||||
| chr1:15281760
|
C | CA | 34 | a0001c0001t0002g0040a0001c0001t0008g0127a0001c0001t0012g0161others(31): Show | 34 | HG01099.hp1 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.301-7615dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15281760 | |||||
| chr1:15281760
|
C | CAA | 10 | a0001c0001t0013g0104a0002c0035t0006g0026a0002c0080t0019g0181others(7): Show | 10 | HG02055.hp2 HG02615.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.301-7616_301-7615d others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15281760 | |||||
| chr1:15281760
|
C | CAAA | 12 | a0001c0001t0008g0175a0001c0002t0049g0101a0002c0003t0005g0172others(9): Show | 12 | HG02040.hp2 HG02083.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.301-7617_301-7615d others(5): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15281760 | |||||
| chr1:15281760
|
CA | C | 65 | a0001c0001t0002g0054a0001c0001t0010g0281a0001c0002t0001g0038others(62): Show | 65 | HG00609.hp1 HG00642.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.301-7615delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15281760 | |||||
| chr1:15281760
|
CAAAAAAA others(3): Show |
C | 5 | a0002c0018t0007g0140a0003c0085t0055g0139a0006c0014t0005g0255others(2): Show | 5 | HG00642.hp2 HG02630.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-7624_301-7615d others(12): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15281760 | |||||
| chr1:15281922
|
C | T | 51 | a0001c0001t0008g0175a0001c0001t0013g0104a0001c0001t0057g0250others(48): Show | 51 | HG01099.hp1 HG01106.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.301-7477C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15281922 | ||||||
| chr1:15282057
|
C | T | 15 | a0001c0001t0013g0104a0001c0002t0049g0101a0001c0090t0048g0158others(12): Show | 15 | HG02145.hp2 HG02615.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.301-7342C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15282057 | ||||||
| chr1:15282257
|
G | A | 51 | a0001c0032t0023g0282a0005c0005t0010g0274a0005c0005t0010g0277others(48): Show | 51 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.301-7142G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15282257 | ||||||
| chr1:15282301
|
G | T | 51 | a0001c0032t0023g0282a0005c0005t0010g0274a0005c0005t0010g0277others(48): Show | 51 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.301-7098G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15282301 | ||||||
| chr1:15282381
|
G | T | 51 | a0001c0032t0023g0282a0005c0005t0010g0274a0005c0005t0010g0277others(48): Show | 51 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.301-7018G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15282381 | ||||||
| chr1:15282392
|
C | T | 51 | a0001c0032t0023g0282a0005c0005t0010g0274a0005c0005t0010g0277others(48): Show | 51 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.301-7007C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15282392 | ||||||
| chr1:15282399
|
T | C | 51 | a0001c0032t0023g0282a0005c0005t0010g0274a0005c0005t0010g0277others(48): Show | 51 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.301-7000T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15282399 | ||||||
| chr1:15282451
|
C | T | 8 | a0001c0001t0057g0250a0002c0080t0019g0181a0002c0081t0058g0251others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.301-6948C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15282451 | ||||||
| chr1:15282523
|
T | G | 16 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0012g0126others(13): Show | 16 | HG01106.hp2 HG01192.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.301-6876T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15282523 | ||||||
| chr1:15282585
|
A | G | 7 | a0060c0065t0043g0005a0061c0066t0040g0003a0062c0062t0011g0285others(4): Show | 7 | HG01099.hp1 HG01106.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.301-6814A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15282585 | ||||||
| chr1:15282621
|
T | G | 51 | a0001c0032t0023g0282a0005c0005t0010g0274a0005c0005t0010g0277others(48): Show | 51 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.301-6778T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15282621 | ||||||
| chr1:15282645
|
G | T | 2 | a0002c0019t0027g0244a0004c0087t0046g0121 | 2 | HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.301-6754G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15282645 | ||||||
| chr1:15282649
|
A | T | 23 | a0001c0001t0008g0149a0001c0002t0001g0188a0006c0014t0003g0214others(20): Show | 23 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.301-6750A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15282649 | ||||||
| chr1:15283210
|
C | T | 9 | a0014c0110t0008g0254a0014c0112t0007g0202a0014c0118t0007g0198others(6): Show | 9 | HG01167.hp1 HG01243.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.301-6189C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15283210 | ||||||
| chr1:15283224
|
C | A | 1 | a0002c0003t0005g0177 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.301-6175C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15283224 | ||||||
| chr1:15283432
|
C | T | 11 | a0014c0110t0008g0254a0014c0112t0007g0202a0014c0118t0007g0198others(8): Show | 11 | HG01167.hp1 HG01243.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.301-5967C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15283432 | ||||||
| chr1:15283508
|
T | C | 130 | a0001c0001t0002g0049a0001c0001t0002g0054a0001c0001t0002g0057others(127): Show | 130 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.301-5891T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15283508 | ||||||
| chr1:15283573
|
G | T | 2 | a0001c0108t0001g0165a0004c0096t0002g0033 | 2 | HG02135.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.301-5826G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15283573 | ||||||
| chr1:15283674
|
G | A | 88 | a0001c0001t0002g0049a0001c0001t0002g0054a0001c0001t0002g0057others(85): Show | 88 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.301-5725G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15283674 | ||||||
| chr1:15283675
|
C | T | 20 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0008g0160others(17): Show | 20 | HG01106.hp2 HG01192.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.301-5724C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15283675 | ||||||
| chr1:15283696
|
G | T | 27 | a0001c0001t0008g0175a0001c0001t0057g0250a0002c0003t0003g0192others(24): Show | 27 | HG00642.hp2 HG02040.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.301-5703G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15283696 | ||||||
| chr1:15283770
|
A | G | 180 | a0001c0001t0002g0049a0001c0001t0002g0054a0001c0001t0002g0057others(177): Show | 180 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.301-5629A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15283770 | ||||||
| chr1:15283888
|
A | C | 1 | a0021c0113t0016g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.301-5511A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15283888 | ||||||
| chr1:15284113
|
G | A | 239 | a0001c0001t0002g0049a0001c0001t0002g0054a0001c0001t0002g0057others(236): Show | 239 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(236): Show |
intron_variant | MODIFIER | c.301-5286G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15284113 | ||||||
| chr1:15284335
|
C | T | 1 | a0016c0107t0003g0145 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.301-5064C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15284335 | ||||||
| chr1:15284351
|
C | T | 88 | a0001c0001t0002g0049a0001c0001t0002g0054a0001c0001t0002g0057others(85): Show | 88 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.301-5048C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15284351 | ||||||
| chr1:15284458
|
G | GA | 8 | a0001c0002t0018g0156a0001c0032t0014g0152a0001c0102t0012g0146others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.301-4940dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15284458 | |||||
| chr1:15284478
|
C | CAA | 82 | a0001c0001t0008g0160a0001c0001t0012g0126a0001c0001t0012g0128others(79): Show | 82 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.301-4904_301-4903d others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15284478 | |||||
| chr1:15284478
|
C | CAAA | 135 | a0001c0001t0002g0049a0001c0001t0002g0054a0001c0001t0002g0057others(132): Show | 135 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.301-4905_301-4903d others(5): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15284478 | |||||
| chr1:15284478
|
C | CAAAA | 8 | a0001c0013t0001g0045a0003c0009t0028g0191a0004c0004t0004g0024others(5): Show | 8 | HG02055.hp2 HG02056.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.301-4906_301-4903d others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15284478 | |||||
| chr1:15284552
|
CT | C | 3 | a0001c0002t0001g0102a0013c0021t0013g0056a0057c0105t0004g0059 | 3 | HG01106.hp2 HG02451.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.301-4845delT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15284552 | |||||
| chr1:15284622
|
G | A | 122 | a0001c0001t0002g0049a0001c0001t0002g0054a0001c0001t0002g0057others(119): Show | 122 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.301-4777G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15284622 | ||||||
| chr1:15284697
|
C | T | 11 | a0001c0001t0008g0175a0002c0003t0003g0192a0002c0003t0005g0172others(8): Show | 11 | HG02040.hp2 HG02083.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.301-4702C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15284697 | ||||||
| chr1:15284701
|
G | A | 2 | a0003c0006t0002g0046a0004c0004t0004g0024 | 2 | NA18978.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.301-4698G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15284701 | ||||||
| chr1:15284879
|
A | G | 4 | a0001c0001t0008g0160a0001c0001t0012g0161a0001c0002t0009g0162others(1): Show | 4 | HG03017.hp1 HG03654.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-4520A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15284879 | ||||||
| chr1:15284917
|
A | G | 1 | a0004c0004t0004g0168 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.301-4482A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15284917 | ||||||
| chr1:15284923
|
GGAAA | G | 46 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0008g0149others(43): Show | 46 | HG00673.hp1 HG00673.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.301-4461_301-4458d others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15284923 | |||||
| chr1:15285004
|
G | A | 1 | a0012c0079t0027g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.301-4395G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15285004 | ||||||
| chr1:15285008
|
A | G | 1 | a0004c0004t0004g0067 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.301-4391A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15285008 | ||||||
| chr1:15285096
|
A | G | 1 | a0012c0051t0011g0284 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.301-4303A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15285096 | ||||||
| chr1:15285097
|
T | C | 11 | a0001c0001t0008g0175a0002c0003t0003g0192a0002c0003t0005g0172others(8): Show | 11 | HG02040.hp2 HG02083.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.301-4302T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15285097 | ||||||
| chr1:15285257
|
C | T | 3 | a0002c0080t0019g0181a0007c0012t0016g0187a0007c0082t0016g0180 | 3 | HG02896.hp1 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.301-4142C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15285257 | ||||||
| chr1:15285325
|
G | A | 224 | a0001c0001t0002g0049a0001c0001t0002g0054a0001c0001t0002g0057others(221): Show | 224 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(221): Show |
intron_variant | MODIFIER | c.301-4074G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15285325 | ||||||
| chr1:15285414
|
T | C | 2 | a0006c0014t0003g0224a0022c0046t0009g0222 | 2 | HG02132.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.301-3985T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15285414 | ||||||
| chr1:15285428
|
G | A | 4 | a0001c0001t0013g0104a0001c0002t0049g0101a0007c0033t0014g0068others(1): Show | 4 | HG02145.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.301-3971G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15285428 | ||||||
| chr1:15285464
|
C | T | 1 | a0020c0111t0030g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.301-3935C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15285464 | ||||||
| chr1:15285482
|
G | A | 1 | a0008c0122t0009g0215 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.301-3917G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15285482 | ||||||
| chr1:15285534
|
C | CATAA | 11 | a0001c0001t0057g0250a0002c0019t0027g0244a0002c0080t0019g0181others(8): Show | 11 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.301-3848_301-3845d others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr1 | 15285534 | |||||
| chr1:15285615
|
C | A | 1 | a0001c0002t0001g0079 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.301-3784C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15285615 | ||||||
| chr1:15285729
|
G | A | 7 | a0001c0001t0013g0072a0001c0001t0013g0092a0003c0006t0013g0060others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.301-3670G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15285729 | ||||||
| chr1:15285794
|
G | C | 2 | a0002c0019t0027g0244a0004c0087t0046g0121 | 2 | HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.301-3605G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15285794 | ||||||
| chr1:15285917
|
G | A | 8 | a0001c0001t0057g0250a0002c0080t0019g0181a0002c0081t0058g0251others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.301-3482G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15285917 | ||||||
| chr1:15286035
|
C | G | 123 | a0001c0001t0002g0049a0001c0001t0002g0054a0001c0001t0002g0057others(120): Show | 123 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.301-3364C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15286035 | ||||||
| chr1:15286547
|
G | A | 1 | a0036c0121t0007g0201 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.301-2852G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15286547 | ||||||
| chr1:15286615
|
C | G | 1 | a0002c0003t0005g0177 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.301-2784C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15286615 | ||||||
| chr1:15286823
|
C | T | 50 | a0005c0005t0010g0274a0005c0005t0010g0277a0005c0005t0010g0279others(47): Show | 50 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.301-2576C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15286823 | ||||||
| chr1:15286982
|
G | A | 165 | a0001c0001t0002g0049a0001c0001t0002g0054a0001c0001t0002g0057others(162): Show | 165 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.301-2417G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15286982 | ||||||
| chr1:15287035
|
A | G | 1 | a0003c0009t0001g0035 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.301-2364A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15287035 | ||||||
| chr1:15287133
|
C | A | 2 | a0009c0011t0019g0144a0028c0109t0007g0197 | 2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.301-2266C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15287133 | ||||||
| chr1:15287147
|
T | C | 216 | a0001c0001t0002g0049a0001c0001t0002g0054a0001c0001t0002g0057others(213): Show | 216 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(213): Show |
intron_variant | MODIFIER | c.301-2252T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15287147 | ||||||
| chr1:15287148
|
G | A | 4 | a0001c0001t0008g0160a0001c0001t0012g0161a0001c0002t0009g0162others(1): Show | 4 | HG03017.hp1 HG03654.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-2251G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15287148 | ||||||
| chr1:15287209
|
G | A | 50 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0008g0149others(47): Show | 50 | HG00673.hp1 HG00673.hp2 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.301-2190G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15287209 | ||||||
| chr1:15287314
|
A | T | 1 | a0001c0001t0010g0281 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.301-2085A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15287314 | ||||||
| chr1:15287403
|
G | C | 1 | a0002c0019t0027g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.301-1996G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15287403 | ||||||
| chr1:15287411
|
C | T | 6 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0002t0001g0025others(3): Show | 6 | HG01952.hp2 HG02071.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.301-1988C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15287411 | ||||||
| chr1:15287450
|
G | A | 176 | a0001c0001t0002g0054a0001c0001t0002g0057a0001c0001t0002g0081others(173): Show | 176 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.301-1949G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15287450 | ||||||
| chr1:15287468
|
C | T | 1 | a0001c0010t0009g0207 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.301-1931C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15287468 | ||||||
| chr1:15287469
|
G | A | 2 | a0002c0007t0005g0212a0011c0025t0003g0211 | 2 | HG00438.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.301-1930G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15287469 | ||||||
| chr1:15287803
|
G | A | 23 | a0001c0001t0008g0149a0001c0002t0001g0188a0006c0014t0003g0214others(20): Show | 23 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.301-1596G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15287803 | ||||||
| chr1:15288032
|
A | G | 20 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0008g0160others(17): Show | 20 | HG01106.hp2 HG01192.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.301-1367A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15288032 | ||||||
| chr1:15288084
|
G | A | 1 | a0002c0019t0004g0118 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.301-1315G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15288084 | ||||||
| chr1:15288198
|
A | T | 2 | a0002c0007t0003g0190a0004c0057t0005g0189 | 2 | NA18964.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.301-1201A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15288198 | ||||||
| chr1:15288225
|
G | T | 1 | a0007c0012t0016g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.301-1174G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15288225 | ||||||
| chr1:15288377
|
T | C | 7 | a0001c0002t0018g0156a0001c0032t0014g0152a0001c0102t0012g0146others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.301-1022T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15288377 | ||||||
| chr1:15288419
|
C | T | 6 | a0002c0003t0005g0177a0002c0003t0053g0176a0003c0009t0028g0191others(3): Show | 6 | HG02622.hp2 HG03453.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.301-980C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15288419 | ||||||
| chr1:15288616
|
A | G | 25 | a0001c0001t0002g0093a0001c0001t0008g0149a0001c0002t0001g0188others(22): Show | 25 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.301-783A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15288616 | ||||||
| chr1:15288712
|
G | C | 1 | a0002c0003t0004g0044 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.301-687G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15288712 | ||||||
| chr1:15288966
|
G | A | 1 | a0068c0048t0002g0039 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.301-433G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15288966 | ||||||
| chr1:15289044
|
G | A | 4 | a0001c0002t0001g0023a0003c0006t0002g0018a0004c0004t0004g0027others(1): Show | 4 | HG00544.hp2 NA18994.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-355G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15289044 | ||||||
| chr1:15289087
|
T | G | 4 | a0001c0001t0008g0160a0001c0001t0012g0161a0001c0002t0009g0162others(1): Show | 4 | HG03017.hp1 HG03654.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-312T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15289087 | ||||||
| chr1:15289174
|
G | A | 1 | a0010c0043t0005g0013 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.301-225G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15289174 | ||||||
| chr1:15289333
|
G | C | 2 | a0042c0069t0023g0293a0043c0068t0011g0292 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.301-66G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 3/33 | chr1 | 15289333 | ||||||
| chr1:15289687
|
T | C | 141 | a0001c0001t0002g0093a0001c0001t0008g0127a0001c0001t0008g0129others(138): Show | 141 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(138): Show |
intron_variant | MODIFIER | c.568+21T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15289687 | ||||||
| chr1:15289875
|
C | T | 8 | a0001c0001t0057g0250a0002c0080t0019g0181a0002c0081t0058g0251others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+209C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15289875 | ||||||
| chr1:15289933
|
G | T | 1 | a0023c0127t0019g0184 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.568+267G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15289933 | ||||||
| chr1:15290153
|
A | G | 13 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0012g0126others(10): Show | 13 | HG01192.hp2 HG01255.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.568+487A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15290153 | ||||||
| chr1:15290188
|
C | T | 1 | a0006c0014t0005g0220 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.568+522C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15290188 | ||||||
| chr1:15290520
|
C | T | 1 | a0001c0001t0008g0149 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.568+854C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15290520 | ||||||
| chr1:15290558
|
C | T | 92 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0008g0149others(89): Show | 92 | HG00642.hp2 HG00673.hp1 HG00673.hp2 others(89): Show |
intron_variant | MODIFIER | c.568+892C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15290558 | ||||||
| chr1:15290591
|
C | T | 5 | a0001c0001t0002g0081a0002c0003t0006g0083a0003c0006t0002g0090others(2): Show | 5 | HG02165.hp1 NA18981.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.568+925C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15290591 | ||||||
| chr1:15290693
|
AC | A | 16 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0012g0126others(13): Show | 16 | HG01192.hp2 HG01255.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.568+1028delC | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15290693 | ||||||
| chr1:15290694
|
C | CT | 40 | a0001c0001t0002g0093a0001c0001t0008g0149a0001c0001t0008g0175others(37): Show | 40 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(37): Show |
intron_variant | MODIFIER | c.568+1044dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | 15290694 | |||||
| chr1:15290694
|
CT | C | 40 | a0001c0001t0008g0160a0001c0001t0012g0161a0001c0002t0009g0162others(37): Show | 40 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.568+1044delT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | 15290694 | |||||
| chr1:15290695
|
T | C | 2 | a0002c0035t0006g0026a0050c0093t0018g0020 | 2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.568+1029T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15290695 | ||||||
| chr1:15290834
|
G | A | 34 | a0002c0003t0005g0135a0003c0098t0029g0237a0005c0005t0010g0274others(31): Show | 34 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.568+1168G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15290834 | ||||||
| chr1:15290924
|
C | A | 20 | a0001c0001t0002g0093a0001c0001t0008g0149a0001c0002t0001g0188others(17): Show | 20 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.568+1258C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15290924 | ||||||
| chr1:15290992
|
A | G | 2 | a0023c0127t0019g0184a0039c0126t0019g0185 | 2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.568+1326A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15290992 | ||||||
| chr1:15291031
|
T | A | 4 | a0005c0005t0015g0286a0005c0070t0035g0287a0040c0077t0037g0262others(1): Show | 4 | HG02109.hp1 HG02897.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.568+1365T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15291031 | ||||||
| chr1:15291057
|
T | A | 1 | a0001c0001t0013g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.568+1391T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15291057 | ||||||
| chr1:15291105
|
T | C | 17 | a0001c0001t0002g0041a0001c0001t0008g0175a0002c0003t0003g0192others(14): Show | 17 | HG00558.hp2 HG00642.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.568+1439T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15291105 | ||||||
| chr1:15291109
|
C | CT | 51 | a0001c0001t0002g0041a0001c0001t0008g0175a0001c0001t0013g0104others(48): Show | 51 | HG00558.hp2 HG00642.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.568+1461dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | 15291109 | |||||
| chr1:15291109
|
CT | C | 35 | a0001c0001t0013g0028a0002c0003t0004g0017a0003c0006t0002g0122others(32): Show | 35 | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.568+1461delT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | 15291109 | |||||
| chr1:15291240
|
T | C | 121 | a0001c0001t0002g0041a0001c0001t0002g0093a0001c0001t0008g0127others(118): Show | 121 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.568+1574T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15291240 | ||||||
| chr1:15291241
|
T | C | 73 | a0001c0001t0002g0041a0001c0001t0057g0250a0001c0002t0018g0156others(70): Show | 73 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.568+1575T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15291241 | ||||||
| chr1:15291325
|
GC | G | 10 | a0001c0001t0057g0250a0002c0080t0019g0181a0002c0081t0058g0251others(7): Show | 10 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.568+1662delC | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | 15291325 | |||||
| chr1:15291391
|
A | G | 10 | a0001c0001t0057g0250a0002c0080t0019g0181a0002c0081t0058g0251others(7): Show | 10 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.568+1725A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15291391 | ||||||
| chr1:15291418
|
A | G | 2 | a0037c0128t0007g0233a0038c0129t0007g0235 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.568+1752A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15291418 | ||||||
| chr1:15291640
|
C | T | 4 | a0002c0019t0006g0066a0003c0006t0002g0046a0004c0004t0004g0024others(1): Show | 4 | NA18612.hp2 NA18977.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.568+1974C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15291640 | ||||||
| chr1:15291680
|
T | C | 7 | a0001c0002t0018g0156a0001c0032t0014g0152a0001c0102t0012g0146others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.568+2014T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15291680 | ||||||
| chr1:15291939
|
G | A | 1 | a0014c0112t0007g0202 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.568+2273G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15291939 | ||||||
| chr1:15292138
|
CTTTTCTT others(6): Show |
C | 10 | a0001c0001t0057g0250a0002c0080t0019g0181a0002c0081t0058g0251others(7): Show | 10 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.568+2481_568+2493d others(15): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | 15292138 | |||||
| chr1:15292235
|
C | T | 1 | a0007c0012t0016g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.568+2569C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15292235 | ||||||
| chr1:15292321
|
T | TG | 4 | a0003c0098t0029g0237a0023c0127t0019g0184a0039c0126t0019g0185others(1): Show | 4 | HG02257.hp1 HG03471.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.568+2659dupG | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | 15292321 | |||||
| chr1:15292325
|
G | GT | 29 | a0001c0001t0002g0041a0001c0001t0008g0175a0001c0001t0057g0250others(26): Show | 29 | HG00558.hp2 HG00642.hp2 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.568+2667dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | 15292325 | |||||
| chr1:15292402
|
C | T | 4 | a0003c0085t0055g0139a0006c0014t0005g0255a0007c0033t0007g0138others(1): Show | 4 | HG00642.hp2 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.568+2736C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15292402 | ||||||
| chr1:15292411
|
G | T | 1 | a0001c0002t0031g0088 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.568+2745G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15292411 | ||||||
| chr1:15292429
|
G | A | 1 | a0002c0003t0005g0172 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.568+2763G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15292429 | ||||||
| chr1:15292491
|
G | T | 10 | a0001c0001t0057g0250a0002c0080t0019g0181a0002c0081t0058g0251others(7): Show | 10 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.568+2825G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15292491 | ||||||
| chr1:15292541
|
GC | G | 4 | a0003c0085t0055g0139a0006c0014t0005g0255a0007c0033t0007g0138others(1): Show | 4 | HG00642.hp2 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.568+2877delC | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | 15292541 | |||||
| chr1:15292543
|
C | G | 4 | a0003c0085t0055g0139a0006c0014t0005g0255a0007c0033t0007g0138others(1): Show | 4 | HG00642.hp2 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.568+2877C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15292543 | ||||||
| chr1:15292667
|
A | G | 1 | a0001c0008t0012g0205 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.568+3001A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15292667 | ||||||
| chr1:15292765
|
C | G | 31 | a0001c0001t0002g0041a0001c0001t0008g0175a0001c0001t0057g0250others(28): Show | 31 | HG00558.hp2 HG00642.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.568+3099C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15292765 | ||||||
| chr1:15292782
|
T | C | 4 | a0001c0001t0008g0160a0001c0001t0012g0161a0001c0002t0009g0162others(1): Show | 4 | HG03017.hp1 HG03654.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.568+3116T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15292782 | ||||||
| chr1:15292797
|
C | T | 2 | a0008c0044t0009g0218a0035c0124t0029g0217 | 2 | NA19066.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.568+3131C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15292797 | ||||||
| chr1:15292898
|
G | A | 1 | a0001c0002t0001g0025 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.568+3232G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15292898 | ||||||
| chr1:15293074
|
C | T | 1 | a0007c0012t0016g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.568+3408C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293074 | ||||||
| chr1:15293103
|
G | A | 1 | a0002c0003t0005g0172 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.568+3437G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293103 | ||||||
| chr1:15293175
|
C | T | 1 | a0001c0002t0001g0065 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.568+3509C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293175 | ||||||
| chr1:15293263
|
C | T | 35 | a0001c0001t0002g0093a0002c0018t0007g0140a0003c0085t0055g0139others(32): Show | 35 | HG01070.hp1 HG01884.hp2 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.569-3421C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293263 | ||||||
| chr1:15293274
|
A | C | 7 | a0001c0032t0014g0152a0001c0102t0012g0146a0002c0003t0014g0151others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.569-3410A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293274 | ||||||
| chr1:15293289
|
T | C | 1 | a0032c0120t0034g0259 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.569-3395T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293289 | ||||||
| chr1:15293390
|
T | C | 1 | a0021c0113t0016g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.569-3294T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293390 | ||||||
| chr1:15293435
|
T | C | 1 | a0009c0011t0019g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.569-3249T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293435 | ||||||
| chr1:15293446
|
G | A | 51 | a0001c0001t0002g0093a0001c0001t0012g0161a0001c0001t0057g0250others(48): Show | 51 | HG01106.hp1 HG01884.hp2 HG02055.hp2 others(48): Show |
intron_variant | MODIFIER | c.569-3238G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293446 | ||||||
| chr1:15293457
|
T | C | 1 | a0004c0038t0007g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.569-3227T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293457 | ||||||
| chr1:15293487
|
A | C | 1 | a0007c0012t0016g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.569-3197A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293487 | ||||||
| chr1:15293488
|
G | A | 1 | a0007c0012t0016g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.569-3196G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293488 | ||||||
| chr1:15293490
|
A | C | 3 | a0001c0001t0012g0128a0001c0001t0012g0161a0013c0021t0002g0084 | 3 | HG01192.hp2 HG03490.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.569-3194A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293490 | ||||||
| chr1:15293490
|
A | T | 1 | a0007c0012t0016g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.569-3194A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293490 | ||||||
| chr1:15293494
|
C | T | 105 | a0001c0001t0002g0049a0001c0001t0002g0057a0001c0001t0002g0070others(102): Show | 105 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.569-3190C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293494 | ||||||
| chr1:15293502
|
A | G | 1 | a0007c0012t0016g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.569-3182A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293502 | ||||||
| chr1:15293508
|
G | A | 197 | a0001c0001t0002g0040a0001c0001t0002g0049a0001c0001t0002g0057others(194): Show | 197 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(194): Show |
intron_variant | MODIFIER | c.569-3176G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293508 | ||||||
| chr1:15293514
|
C | T | 2 | a0007c0012t0016g0256a0012c0051t0011g0284 | 2 | HG02615.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.569-3170C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293514 | ||||||
| chr1:15293515
|
T | C | 1 | a0007c0012t0016g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.569-3169T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293515 | ||||||
| chr1:15293520
|
C | T | 197 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0054others(194): Show | 197 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(194): Show |
intron_variant | MODIFIER | c.569-3164C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293520 | ||||||
| chr1:15293523
|
G | T | 4 | a0005c0030t0010g0265a0008c0132t0060g0229a0009c0011t0011g0272others(1): Show | 4 | HG02698.hp1 HG03704.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-3161G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293523 | ||||||
| chr1:15293525
|
C | G | 1 | a0008c0044t0009g0223 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.569-3159C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293525 | ||||||
| chr1:15293528
|
A | G | 5 | a0004c0038t0014g0155a0005c0030t0010g0265a0007c0012t0016g0256others(2): Show | 5 | HG02615.hp1 HG02698.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-3156A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293528 | ||||||
| chr1:15293530
|
T | C | 36 | a0001c0001t0013g0104a0001c0001t0057g0250a0001c0002t0018g0156others(33): Show | 36 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.569-3154T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293530 | ||||||
| chr1:15293534
|
A | C | 2 | a0001c0013t0001g0053a0002c0003t0004g0044 | 2 | HG01516.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.569-3150A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293534 | ||||||
| chr1:15293535
|
T | C | 14 | a0002c0018t0021g0247a0003c0085t0055g0139a0007c0012t0026g0245others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.569-3149T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293535 | ||||||
| chr1:15293547
|
A | G | 259 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0054others(256): Show | 259 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(256): Show |
intron_variant | MODIFIER | c.569-3137A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293547 | ||||||
| chr1:15293574
|
T | C | 6 | a0001c0001t0002g0040a0001c0001t0012g0161a0002c0003t0005g0135others(3): Show | 6 | HG02015.hp2 HG02071.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.569-3110T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293574 | ||||||
| chr1:15293586
|
C | T | 2 | a0010c0029t0036g0269a0068c0048t0002g0039 | 2 | HG01496.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.569-3098C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293586 | ||||||
| chr1:15293587
|
A | G | 5 | a0005c0070t0035g0287a0010c0029t0036g0269a0040c0077t0037g0262others(2): Show | 5 | HG01496.hp1 HG02040.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-3097A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293587 | ||||||
| chr1:15293588
|
C | G | 2 | a0001c0001t0002g0057a0068c0048t0002g0039 | 2 | HG01496.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.569-3096C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293588 | ||||||
| chr1:15293588
|
C | T | 2 | a0010c0029t0036g0269a0067c0049t0005g0236 | 2 | HG02040.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.569-3096C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293588 | ||||||
| chr1:15293589
|
G | A | 1 | a0004c0004t0005g0164 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.569-3095G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293589 | ||||||
| chr1:15293611
|
A | G | 5 | a0002c0018t0021g0247a0007c0012t0026g0245a0007c0012t0026g0246others(2): Show | 5 | HG02723.hp1 HG02723.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-3073A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293611 | ||||||
| chr1:15293619
|
G | A | 1 | a0001c0010t0001g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.569-3065G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293619 | ||||||
| chr1:15293666
|
T | C | 3 | a0014c0110t0008g0254a0020c0111t0030g0179a0062c0062t0011g0285 | 3 | HG02572.hp1 HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.569-3018T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293666 | ||||||
| chr1:15293672
|
T | C | 3 | a0014c0110t0008g0254a0020c0111t0030g0179a0062c0062t0011g0285 | 3 | HG02572.hp1 HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.569-3012T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293672 | ||||||
| chr1:15293673
|
G | A | 3 | a0014c0110t0008g0254a0020c0111t0030g0179a0062c0062t0011g0285 | 3 | HG02572.hp1 HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.569-3011G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293673 | ||||||
| chr1:15293674
|
T | C | 3 | a0014c0110t0008g0254a0020c0111t0030g0179a0062c0062t0011g0285 | 3 | HG02572.hp1 HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.569-3010T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293674 | ||||||
| chr1:15293683
|
A | C | 3 | a0060c0065t0043g0005a0064c0063t0030g0195a0065c0064t0041g0006 | 3 | HG01109.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.569-3001A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293683 | ||||||
| chr1:15293726
|
C | A | 61 | a0001c0002t0001g0025a0001c0108t0001g0165a0002c0003t0003g0133others(58): Show | 61 | HG00423.hp2 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.569-2958C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293726 | ||||||
| chr1:15293843
|
C | T | 4 | a0005c0005t0010g0279a0005c0005t0015g0275a0005c0016t0033g0271others(1): Show | 4 | HG00642.hp1 HG00738.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-2841C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293843 | ||||||
| chr1:15293930
|
G | A | 4 | a0014c0110t0008g0254a0025c0042t0003g0010a0025c0042t0003g0011others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-2754G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293930 | ||||||
| chr1:15293966
|
C | T | 1 | a0001c0015t0001g0111 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.569-2718C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15293966 | ||||||
| chr1:15294141
|
T | G | 44 | a0001c0001t0057g0250a0001c0032t0023g0282a0001c0108t0001g0165others(41): Show | 44 | HG00673.hp1 HG01069.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.569-2543T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15294141 | ||||||
| chr1:15294209
|
T | C | 1 | a0001c0002t0031g0088 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.569-2475T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15294209 | ||||||
| chr1:15294237
|
C | G | 30 | a0001c0001t0012g0128a0001c0108t0001g0165a0005c0005t0015g0286others(27): Show | 30 | HG00673.hp1 HG01106.hp2 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.569-2447C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15294237 | ||||||
| chr1:15294340
|
C | T | 1 | a0020c0111t0030g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.569-2344C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15294340 | ||||||
| chr1:15294486
|
C | T | 3 | a0009c0011t0019g0144a0024c0027t0024g0258a0024c0027t0024g0288 | 3 | HG01884.hp1 HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.569-2198C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15294486 | ||||||
| chr1:15294497
|
G | A | 1 | a0001c0002t0001g0019 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.569-2187G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15294497 | ||||||
| chr1:15294580
|
T | C | 10 | a0001c0001t0012g0128a0002c0003t0006g0064a0013c0021t0002g0084others(7): Show | 10 | HG01106.hp2 HG01192.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.569-2104T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15294580 | ||||||
| chr1:15294588
|
T | C | 1 | a0001c0002t0044g0169 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.569-2096T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15294588 | ||||||
| chr1:15294645
|
G | A | 37 | a0001c0001t0012g0126a0001c0010t0001g0097a0001c0010t0001g0098others(34): Show | 37 | HG00423.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.569-2039G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15294645 | ||||||
| chr1:15294890
|
G | T | 1 | a0002c0019t0027g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.569-1794G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15294890 | ||||||
| chr1:15294892
|
C | T | 1 | a0001c0092t0002g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.569-1792C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15294892 | ||||||
| chr1:15295103
|
T | A | 1 | a0001c0108t0001g0165 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.569-1581T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15295103 | ||||||
| chr1:15295158
|
T | TCTTG | 4 | a0015c0023t0008g0123a0015c0023t0008g0130a0015c0023t0008g0131others(1): Show | 4 | HG02132.hp2 NA18960.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.569-1525_569-1522d others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | 15295158 | |||||
| chr1:15295197
|
A | C | 7 | a0001c0001t0057g0250a0001c0032t0023g0282a0005c0070t0035g0287others(4): Show | 7 | HG02280.hp1 HG02717.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.569-1487A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15295197 | ||||||
| chr1:15295212
|
G | T | 126 | a0001c0001t0002g0040a0001c0001t0002g0054a0001c0001t0002g0081others(123): Show | 126 | HG00673.hp1 HG00735.hp2 HG00738.hp2 others(123): Show |
intron_variant | MODIFIER | c.569-1472G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15295212 | ||||||
| chr1:15295470
|
C | T | 2 | a0024c0027t0024g0258a0024c0027t0024g0288 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.569-1214C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15295470 | ||||||
| chr1:15295482
|
C | T | 1 | a0032c0120t0034g0259 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.569-1202C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15295482 | ||||||
| chr1:15295524
|
A | G | 1 | a0003c0056t0001g0107 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.569-1160A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15295524 | ||||||
| chr1:15295634
|
C | CAT | 9 | a0002c0080t0019g0181a0002c0081t0058g0251a0007c0082t0016g0180others(6): Show | 9 | HG01069.hp1 HG01071.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.569-1036_569-1035d others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | 15295634 | |||||
| chr1:15295634
|
C | CATAT | 8 | a0001c0001t0057g0250a0001c0032t0023g0282a0003c0098t0029g0237others(5): Show | 8 | HG02280.hp1 HG02717.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.569-1038_569-1035d others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | 15295634 | |||||
| chr1:15295648
|
T | TATAC | 3 | a0002c0018t0021g0247a0007c0012t0026g0245a0007c0012t0026g0246 | 3 | HG02723.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.569-1035_569-1034i others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | 15295648 | |||||
| chr1:15295650
|
C | T | 2 | a0024c0027t0024g0258a0024c0027t0024g0288 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.569-1034C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15295650 | ||||||
| chr1:15295916
|
G | A | 1 | a0001c0008t0008g0204 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.569-768G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15295916 | ||||||
| chr1:15296094
|
C | T | 4 | a0023c0127t0019g0184a0032c0120t0034g0259a0039c0126t0019g0185others(1): Show | 4 | HG02559.hp1 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-590C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15296094 | ||||||
| chr1:15296251
|
A | AT | 35 | a0001c0001t0002g0049a0001c0001t0014g0052a0001c0002t0001g0078others(32): Show | 35 | HG00558.hp1 HG00735.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.569-413dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | 15296251 | |||||
| chr1:15296251
|
AT | A | 17 | a0001c0001t0012g0126a0001c0001t0012g0128a0001c0010t0001g0182others(14): Show | 17 | HG00735.hp2 HG01192.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.569-413delT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | 15296251 | |||||
| chr1:15296403
|
G | A | 8 | a0013c0021t0002g0084a0013c0021t0008g0136a0013c0021t0013g0056others(5): Show | 8 | HG01106.hp2 HG02451.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-281G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15296403 | ||||||
| chr1:15296464
|
A | G | 3 | a0023c0130t0007g0238a0037c0128t0007g0233a0038c0129t0007g0235 | 3 | HG02622.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.569-220A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15296464 | ||||||
| chr1:15296545
|
G | A | 1 | a0001c0001t0008g0149 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.569-139G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15296545 | ||||||
| chr1:15296548
|
C | T | 10 | a0001c0001t0057g0250a0001c0032t0023g0282a0002c0018t0021g0247others(7): Show | 10 | HG02280.hp1 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.569-136C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15296548 | ||||||
| chr1:15296592
|
G | A | 3 | a0023c0130t0007g0238a0037c0128t0007g0233a0038c0129t0007g0235 | 3 | HG02622.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.569-92G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 4/33 | chr1 | 15296592 | ||||||
| chr1:15296836
|
CGCACT | C | 10 | a0001c0090t0048g0158a0002c0003t0014g0151a0006c0014t0005g0255others(7): Show | 10 | HG00642.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.678+47_678+51delCT others(3): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 15296836 | |||||
| chr1:15296859
|
T | A | 8 | a0002c0003t0006g0157a0003c0098t0029g0237a0009c0011t0019g0144others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.678+66T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15296859 | ||||||
| chr1:15297086
|
A | G | 2 | a0003c0085t0055g0139a0007c0033t0007g0138 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.678+293A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15297086 | ||||||
| chr1:15297159
|
TC | T | 4 | a0023c0127t0019g0184a0032c0120t0034g0259a0039c0126t0019g0185others(1): Show | 4 | HG02559.hp1 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.678+367delC | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15297159 | ||||||
| chr1:15297414
|
C | T | 4 | a0023c0127t0019g0184a0032c0120t0034g0259a0039c0126t0019g0185others(1): Show | 4 | HG02559.hp1 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.678+621C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15297414 | ||||||
| chr1:15297463
|
T | A | 5 | a0001c0001t0002g0041a0001c0001t0002g0057a0003c0009t0001g0035others(2): Show | 5 | HG00544.hp1 HG00558.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.678+670T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15297463 | ||||||
| chr1:15297667
|
A | G | 3 | a0002c0003t0006g0157a0003c0098t0029g0237a0009c0011t0019g0144 | 3 | HG02486.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.678+874A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15297667 | ||||||
| chr1:15297795
|
GT | G | 3 | a0002c0018t0021g0247a0007c0012t0026g0245a0007c0012t0026g0246 | 3 | HG02723.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.678+1009delT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 15297795 | |||||
| chr1:15297908
|
C | T | 19 | a0015c0023t0008g0123a0015c0023t0008g0130a0015c0023t0008g0131others(16): Show | 19 | HG01884.hp1 HG02055.hp2 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.678+1115C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15297908 | ||||||
| chr1:15297909
|
G | A | 3 | a0002c0018t0021g0247a0007c0012t0026g0245a0007c0012t0026g0246 | 3 | HG02723.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.678+1116G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15297909 | ||||||
| chr1:15297994
|
G | C | 2 | a0003c0085t0055g0139a0007c0033t0007g0138 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.678+1201G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15297994 | ||||||
| chr1:15298032
|
C | T | 4 | a0023c0127t0019g0184a0032c0120t0034g0259a0039c0126t0019g0185others(1): Show | 4 | HG02559.hp1 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.678+1239C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15298032 | ||||||
| chr1:15298515
|
A | G | 1 | a0004c0004t0004g0073 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.678+1722A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15298515 | ||||||
| chr1:15298532
|
G | C | 1 | a0020c0111t0030g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.678+1739G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15298532 | ||||||
| chr1:15298893
|
T | A | 4 | a0004c0087t0046g0121a0007c0033t0014g0068a0012c0079t0027g0248others(1): Show | 4 | HG02723.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.678+2100T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15298893 | ||||||
| chr1:15298893
|
T | G | 25 | a0002c0003t0006g0157a0002c0018t0021g0247a0002c0080t0019g0181others(22): Show | 25 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.678+2100T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15298893 | ||||||
| chr1:15298935
|
C | T | 18 | a0002c0003t0006g0157a0002c0080t0019g0181a0002c0081t0058g0251others(15): Show | 18 | HG01069.hp1 HG01071.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.678+2142C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15298935 | ||||||
| chr1:15299005
|
C | CA | 14 | a0001c0001t0008g0175a0001c0002t0001g0058a0001c0002t0001g0061others(11): Show | 14 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.679-2189dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 15299005 | |||||
| chr1:15299011
|
AAAAAACA others(5): Show |
A | 1 | a0007c0033t0007g0138 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.679-2188_679-2177d others(14): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 15299011 | |||||
| chr1:15299012
|
AAAAAC | A | 17 | a0002c0003t0006g0157a0002c0080t0019g0181a0002c0081t0058g0251others(14): Show | 17 | HG01069.hp1 HG01071.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.679-2188_679-2184d others(7): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 15299012 | |||||
| chr1:15299046
|
A | C | 18 | a0002c0003t0006g0157a0002c0080t0019g0181a0002c0081t0058g0251others(15): Show | 18 | HG01069.hp1 HG01071.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.679-2159A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15299046 | ||||||
| chr1:15299059
|
C | A | 18 | a0002c0003t0006g0157a0002c0080t0019g0181a0002c0081t0058g0251others(15): Show | 18 | HG01069.hp1 HG01071.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.679-2146C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15299059 | ||||||
| chr1:15299081
|
C | T | 18 | a0002c0003t0006g0157a0002c0080t0019g0181a0002c0081t0058g0251others(15): Show | 18 | HG01069.hp1 HG01071.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.679-2124C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15299081 | ||||||
| chr1:15299111
|
C | A | 77 | a0001c0001t0057g0250a0001c0032t0023g0282a0001c0090t0048g0158others(74): Show | 77 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.679-2094C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15299111 | ||||||
| chr1:15299199
|
C | CA | 26 | a0001c0001t0002g0049a0001c0001t0002g0081a0001c0002t0001g0019others(23): Show | 26 | HG00642.hp1 HG00738.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.679-1988dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 15299199 | |||||
| chr1:15299199
|
C | CAAA | 14 | a0002c0003t0006g0157a0002c0080t0019g0181a0003c0085t0055g0139others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.679-1990_679-1988d others(5): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 15299199 | |||||
| chr1:15299199
|
C | CAAAA | 11 | a0002c0081t0058g0251a0004c0087t0046g0121a0007c0033t0014g0068others(8): Show | 11 | HG02723.hp2 HG02965.hp1 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.679-1991_679-1988d others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 15299199 | |||||
| chr1:15299199
|
C | CAAAAAAA | 22 | a0001c0001t0057g0250a0001c0032t0023g0282a0002c0035t0006g0026others(19): Show | 22 | HG01884.hp1 HG02132.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.679-1994_679-1988d others(9): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 15299199 | |||||
| chr1:15299199
|
C | CAAAAAAA others(1): Show |
12 | a0001c0090t0048g0158a0005c0070t0035g0287a0006c0014t0005g0255others(9): Show | 12 | HG00642.hp2 HG01167.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.679-1995_679-1988d others(10): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 15299199 | |||||
| chr1:15299199
|
C | CAAAAAAA others(4): Show |
3 | a0002c0018t0021g0247a0007c0012t0026g0245a0007c0012t0026g0246 | 3 | HG02723.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.679-1998_679-1988d others(13): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 15299199 | |||||
| chr1:15299218
|
G | A | 31 | a0002c0003t0006g0157a0002c0080t0019g0181a0002c0081t0058g0251others(28): Show | 31 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.679-1987G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15299218 | ||||||
| chr1:15299219
|
G | A | 5 | a0013c0021t0002g0084a0013c0021t0008g0136a0013c0021t0013g0056others(2): Show | 5 | HG01106.hp2 HG02451.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.679-1986G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15299219 | ||||||
| chr1:15299220
|
A | G | 26 | a0002c0003t0006g0157a0002c0080t0019g0181a0002c0081t0058g0251others(23): Show | 26 | HG01069.hp1 HG01071.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.679-1985A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15299220 | ||||||
| chr1:15299223
|
A | G | 5 | a0013c0021t0002g0084a0013c0021t0008g0136a0013c0021t0013g0056others(2): Show | 5 | HG01106.hp2 HG02451.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.679-1982A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15299223 | ||||||
| chr1:15299224
|
A | G | 5 | a0013c0021t0002g0084a0013c0021t0008g0136a0013c0021t0013g0056others(2): Show | 5 | HG01106.hp2 HG02451.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.679-1981A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15299224 | ||||||
| chr1:15299324
|
C | T | 26 | a0002c0003t0006g0157a0002c0080t0019g0181a0002c0081t0058g0251others(23): Show | 26 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.679-1881C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15299324 | ||||||
| chr1:15299339
|
C | T | 50 | a0002c0003t0006g0157a0002c0035t0006g0026a0002c0080t0019g0181others(47): Show | 50 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.679-1866C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15299339 | ||||||
| chr1:15299346
|
A | G | 4 | a0004c0087t0046g0121a0007c0033t0014g0068a0012c0079t0027g0248others(1): Show | 4 | HG02723.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.679-1859A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15299346 | ||||||
| chr1:15299608
|
G | A | 2 | a0013c0021t0013g0056a0057c0105t0004g0059 | 2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.679-1597G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15299608 | ||||||
| chr1:15299648
|
G | C | 4 | a0014c0110t0008g0254a0025c0042t0003g0010a0025c0042t0003g0011others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.679-1557G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15299648 | ||||||
| chr1:15299653
|
C | T | 38 | a0001c0001t0057g0250a0001c0032t0023g0282a0001c0090t0048g0158others(35): Show | 38 | HG00642.hp2 HG01167.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.679-1552C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15299653 | ||||||
| chr1:15300107
|
C | CA | 5 | a0002c0035t0006g0026a0023c0130t0007g0238a0037c0128t0007g0233others(2): Show | 5 | HG02622.hp2 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.679-1097dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 15300107 | |||||
| chr1:15300222
|
G | A | 67 | a0001c0090t0048g0158a0001c0102t0012g0146a0002c0003t0006g0157others(64): Show | 67 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(64): Show |
intron_variant | MODIFIER | c.679-983G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15300222 | ||||||
| chr1:15300798
|
C | G | 18 | a0002c0003t0006g0157a0002c0080t0019g0181a0002c0081t0058g0251others(15): Show | 18 | HG01069.hp1 HG01071.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.679-407C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15300798 | ||||||
| chr1:15300851
|
G | A | 1 | a0011c0025t0003g0208 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.679-354G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15300851 | ||||||
| chr1:15300852
|
A | G | 1 | a0003c0006t0013g0060 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.679-353A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15300852 | ||||||
| chr1:15300968
|
T | G | 3 | a0019c0022t0004g0022a0019c0022t0004g0071a0058c0106t0004g0042 | 3 | NA18981.hp1 NA18992.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.679-237T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15300968 | ||||||
| chr1:15300990
|
C | T | 1 | a0007c0012t0016g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.679-215C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15300990 | ||||||
| chr1:15301011
|
G | T | 1 | a0032c0120t0034g0259 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.679-194G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15301011 | ||||||
| chr1:15301094
|
T | C | 10 | a0001c0090t0048g0158a0002c0003t0014g0151a0006c0014t0005g0255others(7): Show | 10 | HG00642.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.679-111T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15301094 | ||||||
| chr1:15301109
|
C | T | 5 | a0019c0022t0018g0015a0023c0127t0019g0184a0032c0120t0034g0259others(2): Show | 5 | HG02559.hp1 HG02970.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.679-96C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15301109 | ||||||
| chr1:15301123
|
C | G | 2 | a0001c0008t0025g0112a0001c0008t0025g0113 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.679-82C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15301123 | ||||||
| chr1:15301125
|
C | T | 3 | a0004c0004t0004g0027a0011c0034t0006g0085a0011c0099t0006g0087 | 3 | HG00558.hp1 NA18944.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.679-80C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15301125 | ||||||
| chr1:15301127
|
G | GCCCCTAC others(304): Show |
5 | a0019c0022t0018g0015a0023c0127t0019g0184a0032c0120t0034g0259others(2): Show | 5 | HG02559.hp1 HG02970.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.679-63_679-62insTT others(309): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr1 | 15301127 | |||||
| chr1:15301173
|
C | T | 1 | a0009c0011t0017g0294 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.679-32C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 5/33 | chr1 | 15301173 | ||||||
| chr1:15301488
|
G | C | 1 | a0001c0001t0002g0093 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.915+47G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15301488 | ||||||
| chr1:15301593
|
C | T | 3 | a0002c0003t0006g0157a0003c0098t0029g0237a0009c0011t0019g0144 | 3 | HG02486.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.915+152C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15301593 | ||||||
| chr1:15301756
|
T | G | 67 | a0001c0090t0048g0158a0001c0102t0012g0146a0002c0003t0006g0157others(64): Show | 67 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(64): Show |
intron_variant | MODIFIER | c.915+315T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15301756 | ||||||
| chr1:15301919
|
T | C | 67 | a0001c0090t0048g0158a0001c0102t0012g0146a0002c0003t0006g0157others(64): Show | 67 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(64): Show |
intron_variant | MODIFIER | c.915+478T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15301919 | ||||||
| chr1:15302005
|
A | T | 1 | a0002c0019t0006g0066 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.915+564A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15302005 | ||||||
| chr1:15302099
|
A | G | 13 | a0013c0021t0002g0084a0013c0021t0008g0136a0013c0021t0013g0056others(10): Show | 13 | HG01106.hp2 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.915+658A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15302099 | ||||||
| chr1:15302121
|
G | C | 3 | a0002c0003t0005g0177a0002c0003t0053g0176a0003c0009t0028g0191 | 3 | NA18970.hp2 NA18978.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.915+680G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15302121 | ||||||
| chr1:15302182
|
C | T | 11 | a0015c0023t0008g0123a0015c0023t0008g0130a0015c0023t0008g0131others(8): Show | 11 | HG02132.hp1 HG02132.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.915+741C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15302182 | ||||||
| chr1:15302197
|
A | C | 4 | a0014c0110t0008g0254a0025c0042t0003g0010a0025c0042t0003g0011others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.915+756A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15302197 | ||||||
| chr1:15302263
|
G | A | 1 | a0053c0095t0006g0016 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.915+822G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15302263 | ||||||
| chr1:15302460
|
G | A | 1 | a0008c0044t0009g0218 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.915+1019G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15302460 | ||||||
| chr1:15302479
|
G | A | 13 | a0013c0021t0002g0084a0013c0021t0008g0136a0013c0021t0013g0056others(10): Show | 13 | HG01106.hp2 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.915+1038G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15302479 | ||||||
| chr1:15302497
|
A | G | 73 | a0001c0001t0057g0250a0001c0032t0023g0282a0001c0090t0048g0158others(70): Show | 73 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(70): Show |
intron_variant | MODIFIER | c.915+1056A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15302497 | ||||||
| chr1:15302544
|
T | G | 78 | a0001c0001t0002g0040a0001c0001t0002g0054a0001c0001t0002g0081others(75): Show | 78 | HG00673.hp1 HG00735.hp2 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.915+1103T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15302544 | ||||||
| chr1:15302552
|
C | T | 1 | a0003c0098t0029g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.915+1111C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15302552 | ||||||
| chr1:15302593
|
C | T | 8 | a0002c0003t0006g0157a0003c0098t0029g0237a0009c0011t0019g0144others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.915+1152C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15302593 | ||||||
| chr1:15302598
|
G | A | 17 | a0002c0003t0006g0157a0002c0080t0019g0181a0002c0081t0058g0251others(14): Show | 17 | HG01069.hp1 HG01071.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.915+1157G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15302598 | ||||||
| chr1:15302636
|
A | G | 2 | a0005c0070t0035g0287a0060c0065t0043g0005 | 2 | HG02897.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.915+1195A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15302636 | ||||||
| chr1:15302686
|
T | TC | 74 | a0001c0001t0057g0250a0001c0032t0023g0282a0001c0090t0048g0158others(71): Show | 74 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(71): Show |
intron_variant | MODIFIER | c.915+1246dupC | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | INFO_REALIGN_3_PRIME | chr1 | 15302686 | |||||
| chr1:15302850
|
C | T | 4 | a0014c0110t0008g0254a0025c0042t0003g0010a0025c0042t0003g0011others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.915+1409C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15302850 | ||||||
| chr1:15302854
|
G | A | 1 | a0002c0007t0005g0212 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.915+1413G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15302854 | ||||||
| chr1:15302932
|
A | T | 3 | a0002c0080t0019g0181a0007c0082t0016g0180a0066c0061t0042g0007 | 3 | HG02258.hp1 HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.915+1491A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15302932 | ||||||
| chr1:15303187
|
C | G | 13 | a0013c0021t0002g0084a0013c0021t0008g0136a0013c0021t0013g0056others(10): Show | 13 | HG01106.hp2 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.915+1746C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15303187 | ||||||
| chr1:15303243
|
T | A | 6 | a0001c0001t0002g0099a0001c0002t0001g0023a0001c0092t0002g0100others(3): Show | 6 | HG00544.hp2 HG03834.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.915+1802T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15303243 | ||||||
| chr1:15303592
|
G | A | 1 | a0001c0001t0012g0161 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.915+2151G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15303592 | ||||||
| chr1:15303631
|
C | T | 5 | a0019c0022t0018g0015a0023c0127t0019g0184a0032c0120t0034g0259others(2): Show | 5 | HG02559.hp1 HG02970.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.915+2190C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15303631 | ||||||
| chr1:15303647
|
C | T | 3 | a0002c0003t0006g0157a0003c0098t0029g0237a0009c0011t0019g0144 | 3 | HG02486.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.915+2206C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15303647 | ||||||
| chr1:15303648
|
G | A | 5 | a0019c0022t0018g0015a0023c0127t0019g0184a0032c0120t0034g0259others(2): Show | 5 | HG02559.hp1 HG02970.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.915+2207G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15303648 | ||||||
| chr1:15303685
|
C | A | 1 | a0023c0130t0007g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.915+2244C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15303685 | ||||||
| chr1:15303707
|
A | G | 154 | a0001c0001t0002g0040a0001c0001t0002g0054a0001c0001t0002g0081others(151): Show | 154 | HG00642.hp2 HG00673.hp1 HG00735.hp2 others(151): Show |
intron_variant | MODIFIER | c.915+2266A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15303707 | ||||||
| chr1:15303816
|
T | C | 43 | a0001c0001t0057g0250a0001c0032t0023g0282a0001c0090t0048g0158others(40): Show | 43 | HG00642.hp2 HG01167.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.915+2375T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15303816 | ||||||
| chr1:15303848
|
C | CA | 48 | a0001c0001t0057g0250a0001c0032t0023g0282a0001c0090t0048g0158others(45): Show | 48 | HG00642.hp2 HG01106.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.915+2422dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | INFO_REALIGN_3_PRIME | chr1 | 15303848 | |||||
| chr1:15303860
|
A | G | 1 | a0001c0002t0031g0088 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.915+2419A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15303860 | ||||||
| chr1:15304187
|
G | A | 1 | a0009c0011t0019g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.915+2746G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15304187 | ||||||
| chr1:15304609
|
A | G | 8 | a0019c0022t0018g0015a0023c0127t0019g0184a0023c0130t0007g0238others(5): Show | 8 | HG02559.hp1 HG02622.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.915+3168A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15304609 | ||||||
| chr1:15304686
|
A | T | 1 | a0051c0100t0001g0091 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.915+3245A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15304686 | ||||||
| chr1:15304705
|
T | A | 1 | a0005c0016t0028g0009 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.915+3264T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15304705 | ||||||
| chr1:15304751
|
G | A | 2 | a0064c0063t0030g0195a0065c0064t0041g0006 | 2 | HG01109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.915+3310G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15304751 | ||||||
| chr1:15304858
|
G | T | 1 | a0003c0009t0028g0191 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.915+3417G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15304858 | ||||||
| chr1:15304859
|
A | C | 1 | a0003c0009t0028g0191 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.915+3418A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15304859 | ||||||
| chr1:15304878
|
T | G | 1 | a0003c0009t0028g0191 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.915+3437T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15304878 | ||||||
| chr1:15304883
|
G | A | 1 | a0003c0009t0028g0191 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.915+3442G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15304883 | ||||||
| chr1:15304936
|
C | T | 16 | a0013c0021t0002g0084a0013c0021t0008g0136a0013c0021t0013g0056others(13): Show | 16 | HG01106.hp2 HG02451.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.915+3495C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15304936 | ||||||
| chr1:15304950
|
TGTC | T | 77 | a0001c0001t0002g0070a0001c0001t0002g0099a0001c0001t0008g0127others(74): Show | 77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.915+3511_915+3513d others(5): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | INFO_REALIGN_3_PRIME | chr1 | 15304950 | |||||
| chr1:15304953
|
CG | C | 3 | a0001c0013t0001g0051a0012c0041t0003g0124a0063c0067t0039g0004 | 3 | HG01081.hp1 HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.915+3516delG | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | INFO_REALIGN_3_PRIME | chr1 | 15304953 | |||||
| chr1:15304956
|
G | T | 1 | a0003c0006t0002g0090 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.915+3515G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15304956 | ||||||
| chr1:15305153
|
G | A | 8 | a0013c0021t0002g0084a0013c0021t0008g0136a0013c0021t0013g0056others(5): Show | 8 | HG01106.hp2 HG02451.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.916-3460G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15305153 | ||||||
| chr1:15305275
|
T | C | 8 | a0019c0022t0018g0015a0023c0127t0019g0184a0023c0130t0007g0238others(5): Show | 8 | HG02559.hp1 HG02622.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.916-3338T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15305275 | ||||||
| chr1:15305377
|
C | T | 2 | a0005c0070t0035g0287a0060c0065t0043g0005 | 2 | HG02897.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.916-3236C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15305377 | ||||||
| chr1:15305457
|
G | C | 1 | a0027c0094t0001g0082 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.916-3156G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15305457 | ||||||
| chr1:15305470
|
C | T | 8 | a0002c0003t0006g0157a0003c0098t0029g0237a0009c0011t0019g0144others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.916-3143C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15305470 | ||||||
| chr1:15305493
|
C | G | 1 | a0001c0102t0012g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.916-3120C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15305493 | ||||||
| chr1:15305530
|
T | C | 2 | a0004c0004t0007g0001a0004c0004t0007g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.916-3083T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15305530 | ||||||
| chr1:15305787
|
A | G | 1 | a0002c0003t0006g0157 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.916-2826A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15305787 | ||||||
| chr1:15305838
|
C | T | 3 | a0002c0018t0021g0247a0007c0012t0026g0245a0007c0012t0026g0246 | 3 | HG02723.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.916-2775C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15305838 | ||||||
| chr1:15306096
|
G | C | 6 | a0026c0031t0003g0252a0026c0031t0003g0253a0028c0109t0007g0197others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.916-2517G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15306096 | ||||||
| chr1:15306099
|
C | T | 10 | a0015c0023t0008g0123a0015c0023t0008g0130a0015c0023t0008g0131others(7): Show | 10 | HG02132.hp1 HG02145.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.916-2514C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15306099 | ||||||
| chr1:15306296
|
C | T | 18 | a0002c0003t0006g0157a0002c0080t0019g0181a0002c0081t0058g0251others(15): Show | 18 | HG01069.hp1 HG01071.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.916-2317C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15306296 | ||||||
| chr1:15306356
|
G | T | 1 | a0002c0007t0006g0115 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.916-2257G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15306356 | ||||||
| chr1:15306357
|
C | T | 1 | a0002c0007t0006g0115 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.916-2256C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15306357 | ||||||
| chr1:15306560
|
G | A | 1 | a0039c0126t0019g0185 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.916-2053G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15306560 | ||||||
| chr1:15306561
|
G | C | 28 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(25): Show | 28 | HG01884.hp1 HG02055.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.916-2052G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15306561 | ||||||
| chr1:15306570
|
G | A | 8 | a0013c0021t0002g0084a0013c0021t0008g0136a0013c0021t0013g0056others(5): Show | 8 | HG01106.hp2 HG02451.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.916-2043G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15306570 | ||||||
| chr1:15306650
|
A | G | 16 | a0013c0021t0002g0084a0013c0021t0008g0136a0013c0021t0013g0056others(13): Show | 16 | HG01106.hp2 HG02451.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.916-1963A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15306650 | ||||||
| chr1:15306715
|
G | C | 1 | a0032c0120t0034g0259 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.916-1898G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15306715 | ||||||
| chr1:15306925
|
G | A | 3 | a0002c0018t0021g0247a0007c0012t0026g0245a0007c0012t0026g0246 | 3 | HG02723.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.916-1688G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15306925 | ||||||
| chr1:15307066
|
G | A | 1 | a0001c0001t0002g0093 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.916-1547G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15307066 | ||||||
| chr1:15307101
|
C | T | 1 | a0001c0102t0012g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.916-1512C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15307101 | ||||||
| chr1:15307212
|
T | G | 16 | a0013c0021t0002g0084a0013c0021t0008g0136a0013c0021t0013g0056others(13): Show | 16 | HG01106.hp2 HG02451.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.916-1401T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15307212 | ||||||
| chr1:15307321
|
G | A | 26 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(23): Show | 26 | HG01884.hp1 HG02055.hp2 HG02132.hp1 others(23): Show |
intron_variant | MODIFIER | c.916-1292G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15307321 | ||||||
| chr1:15307350
|
C | T | 1 | a0007c0101t0014g0119 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.916-1263C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15307350 | ||||||
| chr1:15307734
|
C | CT | 8 | a0001c0002t0001g0019a0013c0021t0002g0084a0013c0021t0008g0136others(5): Show | 8 | HG01106.hp2 HG02451.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.916-866dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | INFO_REALIGN_3_PRIME | chr1 | 15307734 | |||||
| chr1:15307754
|
G | A | 8 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(5): Show | 8 | HG02280.hp1 HG02717.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.916-859G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15307754 | ||||||
| chr1:15307793
|
C | T | 7 | a0002c0018t0007g0140a0017c0017t0007g0008a0017c0017t0007g0147others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.916-820C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15307793 | ||||||
| chr1:15307824
|
G | A | 1 | a0002c0003t0005g0135 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.916-789G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15307824 | ||||||
| chr1:15307845
|
C | T | 8 | a0019c0022t0018g0015a0023c0127t0019g0184a0023c0130t0007g0238others(5): Show | 8 | HG02559.hp1 HG02622.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.916-768C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15307845 | ||||||
| chr1:15307931
|
C | T | 2 | a0004c0004t0007g0001a0004c0004t0007g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.916-682C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15307931 | ||||||
| chr1:15307977
|
G | A | 2 | a0002c0035t0006g0026a0050c0093t0018g0020 | 2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.916-636G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15307977 | ||||||
| chr1:15308025
|
C | T | 2 | a0001c0001t0012g0161a0008c0122t0009g0215 | 2 | HG04204.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.916-588C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15308025 | ||||||
| chr1:15308157
|
G | C | 2 | a0002c0035t0006g0026a0050c0093t0018g0020 | 2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.916-456G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15308157 | ||||||
| chr1:15308173
|
T | C | 292 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(289): Show | 292 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(289): Show |
intron_variant | MODIFIER | c.916-440T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15308173 | ||||||
| chr1:15308245
|
T | C | 2 | a0001c0001t0015g0267a0001c0013t0011g0266 | 2 | HG01433.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.916-368T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15308245 | ||||||
| chr1:15308300
|
A | G | 75 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(72): Show | 75 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(72): Show |
intron_variant | MODIFIER | c.916-313A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15308300 | ||||||
| chr1:15308351
|
C | T | 3 | a0001c0008t0008g0204a0002c0007t0003g0186a0067c0049t0005g0236 | 3 | HG02056.hp2 NA18956.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.916-262C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15308351 | ||||||
| chr1:15308472
|
T | G | 41 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(38): Show | 41 | HG00642.hp2 HG01167.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.916-141T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15308472 | ||||||
| chr1:15308490
|
T | C | 1 | a0001c0001t0015g0267 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.916-123T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15308490 | ||||||
| chr1:15308585
|
C | A | 2 | a0008c0047t0059g0230a0008c0132t0060g0229 | 2 | NA18984.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.916-28C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 6/33 | chr1 | 15308585 | ||||||
| chr1:15308775
|
G | A | 2 | a0003c0085t0055g0139a0007c0033t0007g0138 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1039+39G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15308775 | ||||||
| chr1:15308798
|
C | A | 2 | a0001c0102t0012g0146a0004c0038t0014g0155 | 2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1039+62C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15308798 | ||||||
| chr1:15308800
|
G | A | 3 | a0005c0005t0010g0274a0005c0005t0010g0277a0010c0029t0017g0276 | 3 | HG01255.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1039+64G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15308800 | ||||||
| chr1:15309004
|
G | T | 24 | a0001c0001t0002g0041a0001c0001t0002g0049a0001c0001t0002g0057others(21): Show | 24 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.1039+268G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15309004 | ||||||
| chr1:15309025
|
C | T | 73 | a0001c0001t0002g0040a0001c0001t0002g0054a0001c0001t0002g0081others(70): Show | 73 | HG00673.hp1 HG00735.hp2 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.1039+289C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15309025 | ||||||
| chr1:15309094
|
G | C | 22 | a0001c0102t0012g0146a0002c0035t0006g0026a0004c0038t0014g0155others(19): Show | 22 | HG01884.hp1 HG02055.hp2 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.1039+358G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15309094 | ||||||
| chr1:15309130
|
C | T | 1 | a0003c0098t0029g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1039+394C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15309130 | ||||||
| chr1:15309322
|
C | T | 3 | a0019c0022t0004g0022a0019c0022t0004g0071a0058c0106t0004g0042 | 3 | NA18981.hp1 NA18992.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1039+586C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15309322 | ||||||
| chr1:15309328
|
C | G | 1 | a0020c0111t0030g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1039+592C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15309328 | ||||||
| chr1:15309585
|
C | T | 14 | a0013c0021t0002g0084a0013c0021t0013g0056a0013c0060t0001g0166others(11): Show | 14 | HG01106.hp2 HG02451.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1039+849C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15309585 | ||||||
| chr1:15309655
|
A | C | 8 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(5): Show | 8 | HG02280.hp1 HG02717.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039+919A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15309655 | ||||||
| chr1:15309660
|
A | AT | 75 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(72): Show | 75 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(72): Show |
intron_variant | MODIFIER | c.1039+936dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | INFO_REALIGN_3_PRIME | chr1 | 15309660 | |||||
| chr1:15309674
|
G | A | 8 | a0002c0003t0006g0157a0003c0098t0029g0237a0009c0011t0019g0144others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1039+938G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15309674 | ||||||
| chr1:15309677
|
AT | A | 17 | a0001c0002t0001g0058a0013c0021t0002g0084a0013c0021t0008g0136others(14): Show | 17 | HG01106.hp2 HG02451.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1039+952delT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | INFO_REALIGN_3_PRIME | chr1 | 15309677 | |||||
| chr1:15309730
|
GC | G | 4 | a0002c0080t0019g0181a0002c0081t0058g0251a0007c0082t0016g0180others(1): Show | 4 | HG02258.hp1 HG02896.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039+997delC | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | INFO_REALIGN_3_PRIME | chr1 | 15309730 | |||||
| chr1:15309786
|
T | C | 16 | a0013c0021t0002g0084a0013c0021t0008g0136a0013c0021t0013g0056others(13): Show | 16 | HG01106.hp2 HG02451.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1039+1050T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15309786 | ||||||
| chr1:15309906
|
G | A | 8 | a0024c0027t0024g0258a0024c0027t0024g0288a0026c0031t0003g0252others(5): Show | 8 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1039+1170G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15309906 | ||||||
| chr1:15309931
|
C | T | 3 | a0019c0022t0004g0022a0019c0022t0004g0071a0058c0106t0004g0042 | 3 | NA18981.hp1 NA18992.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1039+1195C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15309931 | ||||||
| chr1:15310226
|
G | A | 4 | a0002c0080t0019g0181a0002c0081t0058g0251a0007c0082t0016g0180others(1): Show | 4 | HG02258.hp1 HG02896.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039+1490G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15310226 | ||||||
| chr1:15310273
|
C | T | 3 | a0002c0018t0021g0247a0007c0012t0026g0245a0007c0012t0026g0246 | 3 | HG02723.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1039+1537C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15310273 | ||||||
| chr1:15310274
|
G | A | 1 | a0011c0025t0003g0208 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1039+1538G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15310274 | ||||||
| chr1:15310361
|
T | A | 1 | a0001c0010t0001g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1039+1625T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15310361 | ||||||
| chr1:15310369
|
T | C | 4 | a0014c0110t0008g0254a0025c0042t0003g0010a0025c0042t0003g0011others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039+1633T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15310369 | ||||||
| chr1:15310488
|
T | C | 2 | a0002c0003t0004g0017a0002c0134t0003g0209 | 2 | HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1039+1752T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15310488 | ||||||
| chr1:15310736
|
G | A | 2 | a0004c0004t0004g0029a0004c0004t0004g0030 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1039+2000G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15310736 | ||||||
| chr1:15310754
|
C | T | 2 | a0002c0007t0003g0186a0067c0049t0005g0236 | 2 | NA18956.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1039+2018C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15310754 | ||||||
| chr1:15311047
|
C | T | 1 | a0006c0045t0004g0170 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1040-2010C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15311047 | ||||||
| chr1:15311067
|
GAAAC | G | 4 | a0014c0110t0008g0254a0025c0042t0003g0010a0025c0042t0003g0011others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040-1983_1040-198 others(8): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | INFO_REALIGN_3_PRIME | chr1 | 15311067 | |||||
| chr1:15311092
|
T | C | 3 | a0002c0003t0006g0157a0003c0098t0029g0237a0009c0011t0019g0144 | 3 | HG02486.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1040-1965T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15311092 | ||||||
| chr1:15311096
|
C | A | 2 | a0002c0035t0006g0026a0050c0093t0018g0020 | 2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1040-1961C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15311096 | ||||||
| chr1:15311251
|
C | T | 1 | a0003c0037t0001g0094 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1040-1806C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15311251 | ||||||
| chr1:15311508
|
G | A | 75 | a0001c0001t0002g0040a0001c0001t0002g0054a0001c0001t0002g0081others(72): Show | 75 | HG00673.hp1 HG00735.hp2 HG00738.hp2 others(72): Show |
intron_variant | MODIFIER | c.1040-1549G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15311508 | ||||||
| chr1:15311848
|
G | A | 4 | a0014c0110t0008g0254a0025c0042t0003g0010a0025c0042t0003g0011others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040-1209G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15311848 | ||||||
| chr1:15312030
|
G | C | 76 | a0001c0001t0002g0040a0001c0001t0002g0054a0001c0001t0002g0081others(73): Show | 76 | HG00673.hp1 HG00735.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.1040-1027G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15312030 | ||||||
| chr1:15312054
|
G | A | 5 | a0001c0001t0002g0054a0001c0001t0013g0048a0001c0002t0001g0076others(2): Show | 5 | NA18612.hp1 NA18943.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1040-1003G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15312054 | ||||||
| chr1:15312170
|
C | G | 1 | a0036c0121t0007g0201 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1040-887C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15312170 | ||||||
| chr1:15312415
|
C | T | 8 | a0019c0022t0018g0015a0023c0127t0019g0184a0023c0130t0007g0238others(5): Show | 8 | HG02559.hp1 HG02622.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040-642C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15312415 | ||||||
| chr1:15312626
|
T | C | 74 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(71): Show | 74 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(71): Show |
intron_variant | MODIFIER | c.1040-431T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15312626 | ||||||
| chr1:15312758
|
G | A | 6 | a0026c0031t0003g0252a0026c0031t0003g0253a0028c0109t0007g0197others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1040-299G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15312758 | ||||||
| chr1:15312796
|
TC | T | 3 | a0013c0021t0002g0084a0013c0021t0008g0136a0013c0060t0001g0166 | 3 | HG03490.hp1 HG04115.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.1040-258delC | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | INFO_REALIGN_3_PRIME | chr1 | 15312796 | |||||
| chr1:15312930
|
A | G | 1 | a0003c0006t0002g0122 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1040-127A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 7/33 | chr1 | 15312930 | ||||||
| chr1:15313205
|
C | T | 3 | a0013c0021t0002g0084a0013c0021t0008g0136a0013c0060t0001g0166 | 3 | HG03490.hp1 HG04115.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.1170+18C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15313205 | ||||||
| chr1:15313340
|
G | A | 4 | a0001c0002t0001g0061a0001c0002t0001g0065a0001c0002t0001g0150others(1): Show | 4 | HG00621.hp2 NA18986.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+153G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15313340 | ||||||
| chr1:15313424
|
C | T | 10 | a0001c0090t0048g0158a0002c0003t0014g0151a0006c0014t0005g0255others(7): Show | 10 | HG00642.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1170+237C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15313424 | ||||||
| chr1:15313430
|
G | A | 4 | a0023c0130t0007g0238a0032c0120t0034g0259a0037c0128t0007g0233others(1): Show | 4 | HG02622.hp2 HG02970.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1170+243G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15313430 | ||||||
| chr1:15313535
|
G | A | 8 | a0001c0001t0002g0054a0001c0001t0013g0048a0001c0002t0001g0076others(5): Show | 8 | HG03490.hp1 HG04115.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.1170+348G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15313535 | ||||||
| chr1:15313798
|
G | A | 1 | a0010c0029t0017g0276 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1170+611G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15313798 | ||||||
| chr1:15313809
|
C | T | 1 | a0019c0022t0018g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1170+622C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15313809 | ||||||
| chr1:15313823
|
A | G | 8 | a0001c0001t0002g0054a0001c0001t0013g0048a0001c0002t0001g0076others(5): Show | 8 | HG03490.hp1 HG04115.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.1170+636A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15313823 | ||||||
| chr1:15313908
|
T | TA | 23 | a0001c0001t0002g0054a0001c0001t0013g0048a0001c0002t0001g0076others(20): Show | 23 | HG01106.hp2 HG02257.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.1170+726dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr1 | 15313908 | |||||
| chr1:15313953
|
A | G | 239 | a0001c0001t0002g0040a0001c0001t0002g0054a0001c0001t0002g0070others(236): Show | 239 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(236): Show |
intron_variant | MODIFIER | c.1170+766A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15313953 | ||||||
| chr1:15313986
|
G | A | 10 | a0001c0090t0048g0158a0002c0003t0014g0151a0006c0014t0005g0255others(7): Show | 10 | HG00642.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1170+799G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15313986 | ||||||
| chr1:15314061
|
A | AAAT | 11 | a0001c0001t0012g0128a0002c0003t0005g0177a0002c0003t0053g0176others(8): Show | 11 | HG01192.hp2 HG02132.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.1170+913_1170+915d others(5): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr1 | 15314061 | |||||
| chr1:15314061
|
A | AAATAAT | 10 | a0002c0003t0006g0069a0002c0035t0006g0026a0015c0023t0008g0131others(7): Show | 10 | HG02965.hp2 HG02970.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.1170+910_1170+915d others(8): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr1 | 15314061 | |||||
| chr1:15314061
|
AAAT | A | 43 | a0001c0001t0002g0049a0001c0001t0013g0028a0001c0008t0025g0112others(40): Show | 43 | HG00423.hp2 HG00609.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1170+913_1170+915d others(5): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr1 | 15314061 | |||||
| chr1:15314061
|
AAATAAT | A | 13 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(10): Show | 13 | HG02280.hp1 HG02717.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.1170+910_1170+915d others(8): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr1 | 15314061 | |||||
| chr1:15314061
|
AAATAATA others(2): Show |
A | 33 | a0001c0001t0002g0041a0001c0001t0002g0054a0001c0001t0002g0057others(30): Show | 33 | HG00544.hp1 HG00558.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1170+907_1170+915d others(11): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr1 | 15314061 | |||||
| chr1:15314061
|
AAATAATA others(5): Show |
A | 4 | a0001c0013t0001g0051a0005c0005t0015g0268a0005c0072t0010g0270others(1): Show | 4 | HG00735.hp1 HG01081.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+904_1170+915d others(14): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr1 | 15314061 | |||||
| chr1:15314061
|
AAATAATA others(8): Show |
A | 154 | a0001c0001t0002g0040a0001c0001t0002g0070a0001c0001t0002g0081others(151): Show | 154 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.1170+901_1170+915d others(17): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr1 | 15314061 | |||||
| chr1:15314322
|
C | T | 5 | a0002c0003t0006g0083a0002c0007t0003g0190a0004c0004t0004g0067others(2): Show | 5 | NA18964.hp2 NA18986.hp2 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.1170+1135C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15314322 | ||||||
| chr1:15314372
|
C | A | 1 | a0007c0059t0014g0167 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1170+1185C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15314372 | ||||||
| chr1:15314589
|
G | A | 2 | a0002c0003t0006g0157a0009c0011t0019g0144 | 2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1170+1402G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15314589 | ||||||
| chr1:15314635
|
G | GTGGGTGT others(289): Show |
2 | a0002c0003t0006g0157a0009c0011t0019g0144 | 2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1170+1460_1170+146 others(300): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr1 | 15314635 | |||||
| chr1:15314635
|
G | GTGGGTGT others(287): Show |
6 | a0005c0070t0035g0287a0018c0020t0022g0239a0018c0020t0022g0240others(3): Show | 6 | HG02897.hp2 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1170+1460_1170+146 others(298): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr1 | 15314635 | |||||
| chr1:15314635
|
G | GTGGGTGT others(291): Show |
114 | a0001c0001t0002g0041a0001c0001t0002g0049a0001c0001t0002g0054others(111): Show | 114 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.1170+1460_1170+146 others(302): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr1 | 15314635 | |||||
| chr1:15314635
|
G | GTGGGTGT others(309): Show |
1 | a0002c0035t0006g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1170+1460_1170+146 others(320): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr1 | 15314635 | |||||
| chr1:15314635
|
G | GTGGGTGT others(281): Show |
5 | a0014c0110t0008g0254a0020c0111t0030g0179a0025c0042t0003g0010others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1170+1460_1170+146 others(292): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr1 | 15314635 | |||||
| chr1:15314646
|
G | GGAGGGTG others(155): Show |
6 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+1460_1170+146 others(166): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr1 | 15314646 | |||||
| chr1:15314646
|
G | GGAGGGTG others(289): Show |
159 | a0001c0001t0002g0040a0001c0001t0002g0070a0001c0001t0002g0081others(156): Show | 159 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.1170+1460_1170+146 others(300): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr1 | 15314646 | |||||
| chr1:15314648
|
G | T | 6 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+1461G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15314648 | ||||||
| chr1:15314651
|
A | G | 6 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+1464A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15314651 | ||||||
| chr1:15314660
|
T | TG | 6 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+1475dupG | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr1 | 15314660 | |||||
| chr1:15314665
|
T | A | 6 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+1478T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15314665 | ||||||
| chr1:15314669
|
G | T | 6 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+1482G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15314669 | ||||||
| chr1:15314671
|
T | TTG | 6 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+1484_1170+148 others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15314671 | ||||||
| chr1:15314673
|
A | G | 6 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+1486A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15314673 | ||||||
| chr1:15314675
|
T | A | 6 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+1488T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15314675 | ||||||
| chr1:15314687
|
GA | G | 6 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+1501delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15314687 | ||||||
| chr1:15314696
|
G | A | 6 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+1509G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15314696 | ||||||
| chr1:15314703
|
A | G | 6 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+1516A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15314703 | ||||||
| chr1:15314710
|
A | G | 6 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+1523A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15314710 | ||||||
| chr1:15314736
|
G | A | 1 | a0001c0001t0012g0126 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1170+1549G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15314736 | ||||||
| chr1:15314746
|
G | A | 4 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241others(1): Show | 4 | HG02965.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1170+1559G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15314746 | ||||||
| chr1:15314793
|
TGTG | T | 13 | a0001c0001t0002g0054a0001c0001t0013g0048a0001c0002t0001g0076others(10): Show | 13 | HG01106.hp2 HG02451.hp1 HG03490.hp1 others(10): Show |
intron_variant | MODIFIER | c.1171-1583_1171-158 others(7): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr1 | 15314793 | |||||
| chr1:15314810
|
G | C | 1 | a0012c0079t0027g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1171-1568G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15314810 | ||||||
| chr1:15315013
|
T | A | 1 | a0023c0130t0007g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1171-1365T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15315013 | ||||||
| chr1:15315054
|
T | G | 10 | a0001c0090t0048g0158a0002c0003t0014g0151a0003c0085t0055g0139others(7): Show | 10 | HG00642.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1171-1324T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15315054 | ||||||
| chr1:15315055
|
T | C | 10 | a0001c0090t0048g0158a0002c0003t0014g0151a0003c0085t0055g0139others(7): Show | 10 | HG00642.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1171-1323T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15315055 | ||||||
| chr1:15315082
|
T | C | 13 | a0002c0080t0019g0181a0002c0081t0058g0251a0007c0082t0016g0180others(10): Show | 13 | HG01069.hp1 HG01071.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1171-1296T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15315082 | ||||||
| chr1:15315145
|
A | G | 2 | a0003c0085t0055g0139a0007c0033t0007g0138 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1171-1233A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15315145 | ||||||
| chr1:15315476
|
G | A | 2 | a0002c0003t0006g0157a0009c0011t0019g0144 | 2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1171-902G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15315476 | ||||||
| chr1:15315485
|
C | CT | 151 | a0001c0001t0002g0040a0001c0001t0002g0070a0001c0001t0002g0081others(148): Show | 151 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.1171-875dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr1 | 15315485 | |||||
| chr1:15315485
|
C | CTT | 9 | a0001c0001t0008g0127a0001c0002t0044g0169a0001c0108t0001g0165others(6): Show | 9 | HG00735.hp1 HG01106.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1171-876_1171-875d others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr1 | 15315485 | |||||
| chr1:15315485
|
CT | C | 17 | a0002c0018t0021g0247a0002c0080t0019g0181a0002c0081t0058g0251others(14): Show | 17 | HG01069.hp1 HG01071.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1171-875delT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr1 | 15315485 | |||||
| chr1:15315547
|
G | A | 9 | a0001c0102t0012g0146a0003c0098t0029g0237a0004c0038t0014g0155others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1171-831G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15315547 | ||||||
| chr1:15315587
|
G | A | 3 | a0003c0098t0029g0237a0023c0127t0019g0184a0039c0126t0019g0185 | 3 | HG03471.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1171-791G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15315587 | ||||||
| chr1:15315728
|
T | C | 113 | a0001c0001t0002g0040a0001c0001t0002g0054a0001c0001t0002g0070others(110): Show | 113 | HG00544.hp2 HG00642.hp2 HG00673.hp1 others(110): Show |
intron_variant | MODIFIER | c.1171-650T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15315728 | ||||||
| chr1:15315775
|
C | G | 1 | a0023c0127t0019g0184 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1171-603C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15315775 | ||||||
| chr1:15315940
|
C | T | 9 | a0001c0102t0012g0146a0003c0098t0029g0237a0004c0038t0014g0155others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1171-438C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15315940 | ||||||
| chr1:15315955
|
C | T | 3 | a0023c0130t0007g0238a0037c0128t0007g0233a0038c0129t0007g0235 | 3 | HG02622.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1171-423C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15315955 | ||||||
| chr1:15315964
|
G | A | 159 | a0001c0001t0002g0040a0001c0001t0002g0070a0001c0001t0002g0081others(156): Show | 159 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.1171-414G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15315964 | ||||||
| chr1:15316039
|
G | A | 13 | a0001c0001t0002g0054a0001c0001t0013g0048a0001c0002t0001g0076others(10): Show | 13 | HG01106.hp2 HG02451.hp1 HG03490.hp1 others(10): Show |
intron_variant | MODIFIER | c.1171-339G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15316039 | ||||||
| chr1:15316179
|
T | C | 1 | a0012c0079t0027g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1171-199T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15316179 | ||||||
| chr1:15316234
|
C | A | 4 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241others(1): Show | 4 | HG02965.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1171-144C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 8/33 | chr1 | 15316234 | ||||||
| chr1:15316722
|
G | A | 155 | a0001c0001t0002g0040a0001c0001t0002g0070a0001c0001t0002g0081others(152): Show | 155 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.1260+255G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 9/33 | chr1 | 15316722 | ||||||
| chr1:15317116
|
G | A | 1 | a0020c0111t0030g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1260+649G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 9/33 | chr1 | 15317116 | ||||||
| chr1:15317378
|
A | G | 33 | a0001c0001t0002g0054a0001c0001t0013g0048a0001c0002t0001g0076others(30): Show | 33 | HG00642.hp2 HG01106.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.1261-446A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 9/33 | chr1 | 15317378 | ||||||
| chr1:15317510
|
A | C | 2 | a0023c0127t0019g0184a0039c0126t0019g0185 | 2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1261-314A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 9/33 | chr1 | 15317510 | ||||||
| chr1:15317988
|
C | G | 1 | a0022c0046t0009g0193 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1365+60C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15317988 | ||||||
| chr1:15318233
|
C | A | 135 | a0001c0001t0002g0040a0001c0001t0002g0054a0001c0001t0002g0070others(132): Show | 135 | HG00544.hp2 HG00642.hp2 HG00673.hp1 others(132): Show |
intron_variant | MODIFIER | c.1365+305C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15318233 | ||||||
| chr1:15318290
|
A | C | 4 | a0003c0085t0055g0139a0004c0087t0046g0121a0007c0033t0007g0138others(1): Show | 4 | HG02965.hp1 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+362A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15318290 | ||||||
| chr1:15318333
|
G | A | 1 | a0001c0032t0014g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1365+405G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15318333 | ||||||
| chr1:15318397
|
G | T | 3 | a0023c0130t0007g0238a0037c0128t0007g0233a0038c0129t0007g0235 | 3 | HG02622.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1365+469G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15318397 | ||||||
| chr1:15318588
|
C | T | 2 | a0002c0035t0006g0026a0050c0093t0018g0020 | 2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1365+660C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15318588 | ||||||
| chr1:15318593
|
C | T | 1 | a0036c0121t0007g0201 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1365+665C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15318593 | ||||||
| chr1:15318629
|
G | A | 1 | a0020c0116t0052g0200 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1365+701G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15318629 | ||||||
| chr1:15318675
|
T | C | 13 | a0002c0080t0019g0181a0002c0081t0058g0251a0007c0082t0016g0180others(10): Show | 13 | HG01069.hp1 HG01071.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1365+747T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15318675 | ||||||
| chr1:15318697
|
G | A | 1 | a0002c0019t0004g0118 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1365+769G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15318697 | ||||||
| chr1:15318756
|
T | C | 1 | a0064c0063t0030g0195 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1365+828T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15318756 | ||||||
| chr1:15318897
|
C | T | 7 | a0001c0001t0013g0104a0001c0002t0018g0156a0001c0002t0049g0101others(4): Show | 7 | HG01099.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1365+969C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15318897 | ||||||
| chr1:15318912
|
G | T | 7 | a0001c0001t0002g0099a0002c0003t0006g0083a0002c0007t0003g0190others(4): Show | 7 | NA18964.hp2 NA18986.hp2 NA18991.hp1 others(4): Show |
intron_variant | MODIFIER | c.1365+984G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15318912 | ||||||
| chr1:15318993
|
AT | A | 15 | a0001c0032t0023g0282a0002c0080t0019g0181a0002c0081t0058g0251others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1365+1077delT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | INFO_REALIGN_3_PRIME | chr1 | 15318993 | |||||
| chr1:15319055
|
G | C | 137 | a0001c0001t0002g0040a0001c0001t0002g0054a0001c0001t0002g0070others(134): Show | 137 | HG00544.hp2 HG00642.hp2 HG00673.hp1 others(134): Show |
intron_variant | MODIFIER | c.1365+1127G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15319055 | ||||||
| chr1:15319525
|
C | G | 9 | a0001c0001t0002g0099a0002c0003t0006g0083a0002c0007t0003g0190others(6): Show | 9 | NA18964.hp2 NA18966.hp1 NA18983.hp1 others(6): Show |
intron_variant | MODIFIER | c.1365+1597C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15319525 | ||||||
| chr1:15319554
|
G | A | 2 | a0001c0002t0001g0080a0002c0053t0020g0096 | 2 | HG04115.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1365+1626G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15319554 | ||||||
| chr1:15319560
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1365+1632G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15319560 | ||||||
| chr1:15319752
|
G | C | 33 | a0001c0001t0002g0054a0001c0001t0013g0048a0001c0002t0001g0076others(30): Show | 33 | HG00642.hp2 HG01106.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.1365+1824G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15319752 | ||||||
| chr1:15320042
|
C | T | 10 | a0001c0090t0048g0158a0002c0003t0014g0151a0003c0085t0055g0139others(7): Show | 10 | HG00642.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1365+2114C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15320042 | ||||||
| chr1:15320675
|
C | A | 6 | a0026c0031t0003g0252a0026c0031t0003g0253a0028c0109t0007g0197others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1365+2747C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15320675 | ||||||
| chr1:15320972
|
A | G | 3 | a0019c0022t0004g0022a0019c0022t0004g0071a0058c0106t0004g0042 | 3 | NA18981.hp1 NA18992.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1365+3044A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15320972 | ||||||
| chr1:15321137
|
T | C | 7 | a0001c0015t0001g0109a0001c0015t0001g0110a0001c0015t0001g0111others(4): Show | 7 | HG01123.hp2 HG01192.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1365+3209T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15321137 | ||||||
| chr1:15321332
|
C | T | 78 | a0001c0001t0002g0040a0001c0001t0002g0070a0001c0001t0002g0081others(75): Show | 78 | HG00544.hp2 HG00673.hp1 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.1366-3120C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15321332 | ||||||
| chr1:15321378
|
A | G | 162 | a0001c0001t0002g0040a0001c0001t0002g0070a0001c0001t0002g0081others(159): Show | 162 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.1366-3074A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15321378 | ||||||
| chr1:15321518
|
A | G | 1 | a0001c0008t0008g0204 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1366-2934A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15321518 | ||||||
| chr1:15321779
|
TTGTGCAT others(15): Show |
T | 1 | a0002c0018t0018g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1366-2664_1366-264 others(26): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | INFO_REALIGN_3_PRIME | chr1 | 15321779 | |||||
| chr1:15321866
|
T | C | 1 | a0018c0020t0022g0240 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1366-2586T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15321866 | ||||||
| chr1:15322024
|
A | G | 1 | a0002c0134t0003g0209 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1366-2428A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15322024 | ||||||
| chr1:15322036
|
T | G | 167 | a0001c0001t0002g0040a0001c0001t0002g0070a0001c0001t0002g0081others(164): Show | 167 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.1366-2416T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15322036 | ||||||
| chr1:15322049
|
A | AT | 7 | a0002c0080t0019g0181a0002c0081t0058g0251a0007c0082t0016g0180others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366-2397dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | INFO_REALIGN_3_PRIME | chr1 | 15322049 | |||||
| chr1:15322141
|
G | A | 3 | a0019c0022t0004g0022a0019c0022t0004g0071a0058c0106t0004g0042 | 3 | NA18981.hp1 NA18992.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1366-2311G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15322141 | ||||||
| chr1:15322198
|
G | C | 4 | a0014c0110t0008g0254a0025c0042t0003g0010a0025c0042t0003g0011others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366-2254G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15322198 | ||||||
| chr1:15322287
|
G | C | 3 | a0001c0001t0013g0072a0001c0001t0013g0092a0009c0011t0011g0272 | 3 | HG01256.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1366-2165G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15322287 | ||||||
| chr1:15322314
|
C | T | 5 | a0002c0018t0021g0247a0007c0012t0026g0245a0007c0012t0026g0246others(2): Show | 5 | HG01167.hp1 HG01243.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1366-2138C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15322314 | ||||||
| chr1:15322316
|
T | C | 12 | a0015c0023t0008g0123a0015c0023t0008g0130a0015c0023t0008g0131others(9): Show | 12 | HG02132.hp1 HG02132.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1366-2136T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15322316 | ||||||
| chr1:15322535
|
G | A | 63 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0001t0008g0149others(60): Show | 63 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1366-1917G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15322535 | ||||||
| chr1:15322552
|
C | T | 4 | a0003c0085t0055g0139a0004c0087t0046g0121a0007c0033t0007g0138others(1): Show | 4 | HG02965.hp1 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366-1900C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15322552 | ||||||
| chr1:15322704
|
ACCAGACA others(9): Show |
A | 8 | a0001c0090t0048g0158a0002c0003t0014g0151a0006c0014t0005g0255others(5): Show | 8 | HG00642.hp2 HG02055.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1366-1746_1366-173 others(20): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | INFO_REALIGN_3_PRIME | chr1 | 15322704 | |||||
| chr1:15322775
|
A | G | 1 | a0004c0038t0014g0155 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1366-1677A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15322775 | ||||||
| chr1:15322842
|
C | T | 2 | a0004c0004t0007g0001a0004c0004t0007g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1366-1610C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15322842 | ||||||
| chr1:15322871
|
C | T | 1 | a0023c0130t0007g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1366-1581C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15322871 | ||||||
| chr1:15322958
|
A | T | 1 | a0010c0074t0011g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1366-1494A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15322958 | ||||||
| chr1:15322972
|
G | A | 162 | a0001c0001t0002g0049a0001c0001t0002g0054a0001c0001t0002g0081others(159): Show | 162 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.1366-1480G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15322972 | ||||||
| chr1:15322974
|
T | C | 2 | a0010c0029t0017g0276a0033c0131t0005g0219 | 2 | HG01255.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1366-1478T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15322974 | ||||||
| chr1:15323060
|
C | G | 14 | a0001c0001t0057g0250a0001c0010t0001g0182a0002c0018t0021g0247others(11): Show | 14 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1366-1392C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15323060 | ||||||
| chr1:15323427
|
CTG | C | 17 | a0001c0032t0023g0282a0002c0080t0019g0181a0002c0081t0058g0251others(14): Show | 17 | HG02486.hp2 HG02717.hp1 HG02723.hp2 others(14): Show |
intron_variant | MODIFIER | c.1366-1024_1366-102 others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15323427 | ||||||
| chr1:15323470
|
A | G | 82 | a0001c0013t0001g0045a0001c0013t0011g0266a0001c0015t0001g0109others(79): Show | 82 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.1366-982A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15323470 | ||||||
| chr1:15323506
|
G | C | 7 | a0002c0080t0019g0181a0002c0081t0058g0251a0007c0082t0016g0180others(4): Show | 7 | HG02486.hp2 HG02896.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366-946G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15323506 | ||||||
| chr1:15323507
|
C | T | 15 | a0001c0032t0023g0282a0002c0035t0006g0026a0002c0080t0019g0181others(12): Show | 15 | HG02486.hp2 HG02717.hp1 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.1366-945C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15323507 | ||||||
| chr1:15323561
|
C | A | 1 | a0001c0001t0015g0267 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1366-891C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15323561 | ||||||
| chr1:15323633
|
G | C | 6 | a0007c0012t0026g0245a0007c0012t0026g0246a0024c0027t0024g0258others(3): Show | 6 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1366-819G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15323633 | ||||||
| chr1:15323786
|
A | G | 4 | a0026c0031t0003g0252a0026c0031t0003g0253a0042c0069t0023g0293others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366-666A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15323786 | ||||||
| chr1:15323840
|
T | C | 3 | a0019c0022t0004g0022a0019c0022t0004g0071a0058c0106t0004g0042 | 3 | NA18981.hp1 NA18992.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1366-612T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15323840 | ||||||
| chr1:15323868
|
G | A | 2 | a0002c0035t0006g0026a0050c0093t0018g0020 | 2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1366-584G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15323868 | ||||||
| chr1:15323913
|
C | G | 1 | a0020c0111t0030g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1366-539C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15323913 | ||||||
| chr1:15323972
|
T | C | 7 | a0002c0080t0019g0181a0002c0081t0058g0251a0007c0082t0016g0180others(4): Show | 7 | HG02486.hp2 HG02896.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366-480T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15323972 | ||||||
| chr1:15324055
|
C | T | 1 | a0006c0045t0004g0170 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1366-397C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15324055 | ||||||
| chr1:15324118
|
A | G | 1 | a0002c0003t0006g0157 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1366-334A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15324118 | ||||||
| chr1:15324205
|
G | A | 7 | a0002c0080t0019g0181a0002c0081t0058g0251a0007c0082t0016g0180others(4): Show | 7 | HG02486.hp2 HG02896.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366-247G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15324205 | ||||||
| chr1:15324266
|
C | G | 1 | a0020c0111t0030g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1366-186C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15324266 | ||||||
| chr1:15324286
|
C | A | 5 | a0002c0018t0007g0140a0054c0084t0047g0154a0064c0063t0030g0195others(2): Show | 5 | HG01109.hp2 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1366-166C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15324286 | ||||||
| chr1:15324288
|
T | G | 73 | a0001c0013t0001g0045a0001c0013t0001g0051a0001c0013t0001g0053others(70): Show | 73 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.1366-164T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15324288 | ||||||
| chr1:15324295
|
G | C | 73 | a0001c0013t0001g0045a0001c0013t0001g0051a0001c0013t0001g0053others(70): Show | 73 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.1366-157G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15324295 | ||||||
| chr1:15324310
|
C | T | 1 | a0012c0079t0027g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1366-142C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15324310 | ||||||
| chr1:15324416
|
A | G | 2 | a0064c0063t0030g0195a0065c0064t0041g0006 | 2 | HG01109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1366-36A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 10/33 | chr1 | 15324416 | ||||||
| chr1:15324564
|
G | GCATGT | 3 | a0054c0084t0047g0154a0064c0063t0030g0195a0065c0064t0041g0006 | 3 | HG01109.hp2 HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1473+6_1473+10dupC others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | INFO_REALIGN_3_PRIME | chr1 | 15324564 | |||||
| chr1:15324566
|
A | G | 73 | a0001c0013t0001g0045a0001c0013t0001g0051a0001c0013t0001g0053others(70): Show | 73 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(70): Show |
splice_region_variant&intron_variant | LOW | c.1473+7A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15324566 | ||||||
| chr1:15324634
|
G | C | 2 | a0004c0087t0046g0121a0007c0033t0014g0068 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1473+75G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15324634 | ||||||
| chr1:15324781
|
G | A | 1 | a0007c0012t0016g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1473+222G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15324781 | ||||||
| chr1:15324793
|
C | T | 2 | a0001c0090t0048g0158a0002c0003t0014g0151 | 2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1473+234C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15324793 | ||||||
| chr1:15324910
|
A | G | 1 | a0032c0120t0034g0259 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1473+351A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15324910 | ||||||
| chr1:15324923
|
T | C | 37 | a0001c0013t0001g0045a0001c0013t0001g0051a0001c0013t0001g0053others(34): Show | 37 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.1473+364T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15324923 | ||||||
| chr1:15325152
|
G | A | 2 | a0002c0035t0006g0026a0050c0093t0018g0020 | 2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1473+593G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15325152 | ||||||
| chr1:15325330
|
C | T | 1 | a0012c0079t0027g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1473+771C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15325330 | ||||||
| chr1:15325332
|
T | C | 2 | a0008c0125t0012g0196a0010c0074t0011g0261 | 2 | HG01109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1473+773T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15325332 | ||||||
| chr1:15325543
|
A | G | 5 | a0014c0110t0008g0254a0020c0111t0030g0179a0025c0042t0003g0010others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1473+984A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15325543 | ||||||
| chr1:15325610
|
T | C | 83 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0013t0001g0045others(80): Show | 83 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.1473+1051T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15325610 | ||||||
| chr1:15325659
|
A | C | 3 | a0001c0001t0002g0054a0001c0002t0001g0076a0055c0083t0002g0047 | 3 | NA18970.hp1 NA18971.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1473+1100A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15325659 | ||||||
| chr1:15325687
|
G | A | 3 | a0004c0038t0007g0143a0012c0097t0003g0141a0028c0109t0007g0197 | 3 | HG01884.hp2 HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1473+1128G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15325687 | ||||||
| chr1:15325805
|
C | T | 5 | a0001c0032t0023g0282a0003c0085t0055g0139a0004c0087t0046g0121others(2): Show | 5 | HG02717.hp1 HG02965.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1473+1246C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15325805 | ||||||
| chr1:15325900
|
G | A | 1 | a0005c0005t0015g0275 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1474-1159G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15325900 | ||||||
| chr1:15325915
|
A | T | 1 | a0008c0044t0009g0223 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1474-1144A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15325915 | ||||||
| chr1:15326343
|
A | G | 4 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241others(1): Show | 4 | HG02965.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1474-716A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15326343 | ||||||
| chr1:15326568
|
G | C | 6 | a0001c0001t0008g0127a0001c0001t0008g0129a0001c0002t0001g0025others(3): Show | 6 | HG01952.hp1 HG02071.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.1474-491G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15326568 | ||||||
| chr1:15326582
|
A | G | 82 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0013t0001g0045others(79): Show | 82 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.1474-477A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15326582 | ||||||
| chr1:15326671
|
A | G | 1 | a0002c0003t0004g0017 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1474-388A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15326671 | ||||||
| chr1:15326757
|
T | A | 25 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(22): Show | 25 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.1474-302T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15326757 | ||||||
| chr1:15326761
|
C | T | 1 | a0023c0130t0007g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1474-298C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15326761 | ||||||
| chr1:15326835
|
G | A | 4 | a0004c0004t0004g0024a0004c0004t0004g0027a0010c0029t0036g0269others(1): Show | 4 | HG02040.hp1 NA18944.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1474-224G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15326835 | ||||||
| chr1:15326914
|
CGGT | C | 4 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241others(1): Show | 4 | HG02965.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1474-143_1474-141d others(5): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | INFO_REALIGN_3_PRIME | chr1 | 15326914 | |||||
| chr1:15327007
|
A | G | 82 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0013t0001g0045others(79): Show | 82 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.1474-52A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 11/33 | chr1 | 15327007 | ||||||
| chr1:15327153
|
C | T | 1 | a0002c0019t0027g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1557+11C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 12/33 | chr1 | 15327153 | ||||||
| chr1:15327376
|
G | A | 35 | a0001c0013t0001g0045a0001c0013t0001g0051a0001c0013t0001g0053others(32): Show | 35 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1557+234G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 12/33 | chr1 | 15327376 | ||||||
| chr1:15327453
|
C | T | 1 | a0002c0003t0004g0044 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1557+311C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 12/33 | chr1 | 15327453 | ||||||
| chr1:15327499
|
C | T | 1 | a0001c0001t0012g0126 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1557+357C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 12/33 | chr1 | 15327499 | ||||||
| chr1:15327947
|
C | T | 1 | a0008c0125t0012g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1558-330C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 12/33 | chr1 | 15327947 | ||||||
| chr1:15328047
|
AG | A | 30 | a0001c0013t0001g0045a0001c0013t0001g0051a0001c0013t0001g0053others(27): Show | 30 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1558-229delG | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 12/33 | chr1 | 15328047 | ||||||
| chr1:15328048
|
G | A | 48 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(45): Show | 48 | HG01069.hp1 HG01071.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.1558-229G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 12/33 | chr1 | 15328048 | ||||||
| chr1:15328049
|
A | G | 33 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0023g0282others(30): Show | 33 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.1558-228A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 12/33 | chr1 | 15328049 | ||||||
| chr1:15328141
|
C | G | 1 | a0004c0004t0004g0074 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1558-136C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 12/33 | chr1 | 15328141 | ||||||
| chr1:15328225
|
C | T | 2 | a0023c0127t0019g0184a0039c0126t0019g0185 | 2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1558-52C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 12/33 | chr1 | 15328225 | ||||||
| chr1:15328226
|
C | T | 3 | a0019c0022t0004g0022a0019c0022t0004g0071a0058c0106t0004g0042 | 3 | NA18981.hp1 NA18992.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1558-51C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 12/33 | chr1 | 15328226 | ||||||
| chr1:15328241
|
C | CT | 78 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0013t0001g0045others(75): Show | 78 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.1558-22dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 12/33 | INFO_REALIGN_3_PRIME | chr1 | 15328241 | |||||
| chr1:15328442
|
T | G | 2 | a0002c0035t0006g0026a0050c0093t0018g0020 | 2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1710+13T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 13/33 | chr1 | 15328442 | ||||||
| chr1:15328558
|
TCTTGTTG others(6): Show |
T | 1 | a0036c0121t0007g0201 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1710+142_1710+154d others(15): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 13/33 | INFO_REALIGN_3_PRIME | chr1 | 15328558 | |||||
| chr1:15328604
|
A | C | 1 | a0051c0100t0001g0091 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1710+175A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 13/33 | chr1 | 15328604 | ||||||
| chr1:15328616
|
G | A | 1 | a0001c0001t0013g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1710+187G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 13/33 | chr1 | 15328616 | ||||||
| chr1:15328675
|
G | A | 8 | a0014c0110t0008g0254a0018c0020t0022g0239a0018c0020t0022g0240others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1710+246G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 13/33 | chr1 | 15328675 | ||||||
| chr1:15328718
|
A | G | 1 | a0003c0006t0013g0060 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1710+289A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 13/33 | chr1 | 15328718 | ||||||
| chr1:15328795
|
C | T | 18 | a0001c0032t0023g0282a0002c0080t0019g0181a0002c0081t0058g0251others(15): Show | 18 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1710+366C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 13/33 | chr1 | 15328795 | ||||||
| chr1:15328808
|
G | A | 54 | a0001c0001t0002g0054a0001c0001t0008g0127a0001c0001t0008g0129others(51): Show | 54 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1710+379G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 13/33 | chr1 | 15328808 | ||||||
| chr1:15328838
|
G | C | 2 | a0012c0079t0027g0248a0059c0104t0045g0014 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1710+409G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 13/33 | chr1 | 15328838 | ||||||
| chr1:15329093
|
CT | C | 4 | a0003c0086t0009g0142a0005c0070t0035g0287a0046c0078t0007g0232others(1): Show | 4 | HG01070.hp1 HG02280.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1711-250delT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 13/33 | INFO_REALIGN_3_PRIME | chr1 | 15329093 | |||||
| chr1:15329278
|
C | T | 1 | a0005c0005t0010g0279 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1711-68C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 13/33 | chr1 | 15329278 | ||||||
| chr1:15329288
|
G | A | 5 | a0001c0032t0023g0282a0003c0085t0055g0139a0004c0087t0046g0121others(2): Show | 5 | HG02717.hp1 HG02965.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1711-58G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 13/33 | chr1 | 15329288 | ||||||
| chr1:15329704
|
TA | T | 13 | a0004c0004t0004g0024a0004c0004t0004g0027a0007c0012t0026g0245others(10): Show | 13 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1906+174delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | INFO_REALIGN_3_PRIME | chr1 | 15329704 | |||||
| chr1:15329714
|
A | AC | 5 | a0001c0013t0001g0053a0014c0110t0008g0254a0025c0042t0003g0010others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.1906+173_1906+174i others(3): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15329714 | ||||||
| chr1:15329788
|
G | A | 3 | a0001c0092t0002g0100a0004c0004t0004g0074a0067c0049t0005g0236 | 3 | HG00438.hp2 HG03834.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1906+247G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15329788 | ||||||
| chr1:15330025
|
G | T | 1 | a0002c0007t0006g0108 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1906+484G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15330025 | ||||||
| chr1:15330119
|
C | G | 1 | a0007c0101t0014g0119 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1906+578C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15330119 | ||||||
| chr1:15330426
|
GTTCA | G | 8 | a0007c0012t0026g0245a0007c0012t0026g0246a0024c0027t0024g0258others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1906+886_1906+889d others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15330426 | ||||||
| chr1:15330493
|
A | G | 5 | a0002c0080t0019g0181a0007c0082t0016g0180a0017c0017t0007g0008others(2): Show | 5 | HG02486.hp2 HG02896.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1906+952A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15330493 | ||||||
| chr1:15330500
|
G | A | 1 | a0020c0116t0052g0200 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1906+959G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15330500 | ||||||
| chr1:15330563
|
G | A | 2 | a0019c0022t0004g0022a0019c0022t0004g0071 | 2 | NA18992.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1906+1022G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15330563 | ||||||
| chr1:15330624
|
G | A | 2 | a0001c0002t0001g0038a0001c0002t0001g0077 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1906+1083G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15330624 | ||||||
| chr1:15330651
|
C | T | 1 | a0012c0079t0027g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1906+1110C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15330651 | ||||||
| chr1:15330702
|
G | A | 1 | a0067c0049t0005g0236 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1906+1161G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15330702 | ||||||
| chr1:15330710
|
A | G | 78 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0013t0001g0045others(75): Show | 78 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.1906+1169A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15330710 | ||||||
| chr1:15330779
|
G | A | 5 | a0001c0032t0023g0282a0003c0085t0055g0139a0004c0087t0046g0121others(2): Show | 5 | HG02717.hp1 HG02965.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1906+1238G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15330779 | ||||||
| chr1:15330876
|
T | C | 13 | a0002c0080t0019g0181a0002c0081t0058g0251a0007c0082t0016g0180others(10): Show | 13 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1906+1335T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15330876 | ||||||
| chr1:15330929
|
A | G | 1 | a0068c0048t0002g0039 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1906+1388A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15330929 | ||||||
| chr1:15330977
|
G | A | 1 | a0002c0019t0027g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1906+1436G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15330977 | ||||||
| chr1:15331222
|
A | G | 8 | a0007c0012t0026g0245a0007c0012t0026g0246a0024c0027t0024g0258others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1906+1681A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15331222 | ||||||
| chr1:15331236
|
C | T | 1 | a0001c0001t0010g0281 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1906+1695C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15331236 | ||||||
| chr1:15331321
|
A | G | 1 | a0058c0106t0004g0042 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1906+1780A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15331321 | ||||||
| chr1:15331374
|
G | A | 4 | a0014c0110t0008g0254a0025c0042t0003g0010a0025c0042t0003g0011others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1906+1833G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15331374 | ||||||
| chr1:15331434
|
G | A | 1 | a0054c0084t0047g0154 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1906+1893G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15331434 | ||||||
| chr1:15331437
|
C | T | 5 | a0001c0032t0023g0282a0003c0085t0055g0139a0004c0087t0046g0121others(2): Show | 5 | HG02717.hp1 HG02965.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1906+1896C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15331437 | ||||||
| chr1:15331438
|
G | A | 1 | a0001c0002t0001g0058 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1906+1897G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15331438 | ||||||
| chr1:15331480
|
GTGGATTG others(1): Show |
G | 4 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241others(1): Show | 4 | HG02965.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1906+1945_1906+195 others(12): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | INFO_REALIGN_3_PRIME | chr1 | 15331480 | |||||
| chr1:15331485
|
T | C | 3 | a0001c0036t0008g0163a0005c0030t0010g0264a0005c0030t0010g0265 | 3 | HG02698.hp1 HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1906+1944T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15331485 | ||||||
| chr1:15331486
|
TGATG | T | 222 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(219): Show | 222 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.1906+1986_1906+198 others(8): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | INFO_REALIGN_3_PRIME | chr1 | 15331486 | |||||
| chr1:15331486
|
TGATGGAT others(1): Show |
T | 31 | a0001c0001t0013g0104a0001c0032t0023g0282a0002c0003t0005g0135others(28): Show | 31 | HG01069.hp1 HG01071.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.1906+1982_1906+198 others(12): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | INFO_REALIGN_3_PRIME | chr1 | 15331486 | |||||
| chr1:15331486
|
TGATGGAT others(5): Show |
T | 10 | a0001c0090t0048g0158a0002c0003t0014g0151a0002c0080t0019g0181others(7): Show | 10 | HG02055.hp1 HG02486.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1906+1978_1906+198 others(16): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | INFO_REALIGN_3_PRIME | chr1 | 15331486 | |||||
| chr1:15331547
|
T | TGTGG | 4 | a0014c0110t0008g0254a0025c0042t0003g0010a0025c0042t0003g0011others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1906+2019_1906+202 others(8): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | INFO_REALIGN_3_PRIME | chr1 | 15331547 | |||||
| chr1:15331560
|
G | A | 7 | a0001c0001t0057g0250a0001c0010t0001g0182a0002c0018t0021g0247others(4): Show | 7 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1906+2019G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15331560 | ||||||
| chr1:15331615
|
G | A | 1 | a0001c0001t0013g0048 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1906+2074G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15331615 | ||||||
| chr1:15331636
|
CAGGAAGG others(5): Show |
C | 3 | a0019c0022t0004g0022a0019c0022t0004g0071a0058c0106t0004g0042 | 3 | NA18981.hp1 NA18992.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1906+2108_1906+211 others(16): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | INFO_REALIGN_3_PRIME | chr1 | 15331636 | |||||
| chr1:15331649
|
AGGAAGGC others(5): Show |
A | 9 | a0001c0032t0023g0282a0002c0035t0006g0026a0003c0085t0055g0139others(6): Show | 9 | HG01109.hp1 HG02717.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1906+2132_1906+214 others(16): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | INFO_REALIGN_3_PRIME | chr1 | 15331649 | |||||
| chr1:15331691
|
G | A | 4 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241others(1): Show | 4 | HG02965.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1906+2150G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15331691 | ||||||
| chr1:15331697
|
GGGAAGGC others(5): Show |
G | 3 | a0019c0022t0004g0022a0019c0022t0004g0071a0058c0106t0004g0042 | 3 | NA18981.hp1 NA18992.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1906+2168_1906+217 others(16): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | INFO_REALIGN_3_PRIME | chr1 | 15331697 | |||||
| chr1:15331755
|
G | A | 1 | a0061c0066t0040g0003 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1906+2214G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15331755 | ||||||
| chr1:15331802
|
A | G | 3 | a0019c0022t0004g0022a0019c0022t0004g0071a0058c0106t0004g0042 | 3 | NA18981.hp1 NA18992.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1906+2261A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15331802 | ||||||
| chr1:15332043
|
G | A | 1 | a0023c0130t0007g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1906+2502G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15332043 | ||||||
| chr1:15332246
|
G | A | 2 | a0001c0008t0025g0112a0001c0008t0025g0113 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1906+2705G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15332246 | ||||||
| chr1:15332298
|
C | T | 68 | a0001c0013t0001g0045a0001c0013t0001g0051a0001c0013t0001g0053others(65): Show | 68 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.1906+2757C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15332298 | ||||||
| chr1:15332370
|
A | G | 4 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241others(1): Show | 4 | HG02965.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1906+2829A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15332370 | ||||||
| chr1:15332630
|
A | G | 84 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0013t0001g0045others(81): Show | 84 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.1906+3089A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15332630 | ||||||
| chr1:15332712
|
G | A | 5 | a0014c0110t0008g0254a0020c0111t0030g0179a0025c0042t0003g0010others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1906+3171G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15332712 | ||||||
| chr1:15332809
|
A | G | 1 | a0002c0019t0027g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1906+3268A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15332809 | ||||||
| chr1:15333149
|
A | G | 2 | a0002c0003t0004g0017a0002c0134t0003g0209 | 2 | HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1906+3608A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15333149 | ||||||
| chr1:15333444
|
C | T | 1 | a0002c0018t0018g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1906+3903C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15333444 | ||||||
| chr1:15333475
|
T | A | 1 | a0057c0105t0004g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1906+3934T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15333475 | ||||||
| chr1:15333718
|
C | T | 15 | a0002c0018t0007g0140a0014c0110t0008g0254a0018c0020t0022g0239others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1906+4177C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15333718 | ||||||
| chr1:15333742
|
C | A | 7 | a0002c0080t0019g0181a0002c0081t0058g0251a0007c0082t0016g0180others(4): Show | 7 | HG02486.hp2 HG02896.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1906+4201C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15333742 | ||||||
| chr1:15333783
|
C | G | 2 | a0001c0001t0002g0093a0004c0004t0004g0116 | 2 | NA18955.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1906+4242C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15333783 | ||||||
| chr1:15333824
|
C | CT | 46 | a0001c0001t0002g0041a0001c0001t0002g0081a0001c0001t0008g0129others(43): Show | 46 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1906+4309dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | INFO_REALIGN_3_PRIME | chr1 | 15333824 | |||||
| chr1:15333824
|
C | CTT | 20 | a0001c0015t0001g0111a0001c0036t0002g0055a0001c0090t0048g0158others(17): Show | 20 | HG01884.hp2 HG01928.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.1906+4308_1906+430 others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | INFO_REALIGN_3_PRIME | chr1 | 15333824 | |||||
| chr1:15333824
|
C | CTTT | 7 | a0002c0018t0007g0140a0010c0074t0011g0261a0028c0109t0007g0197others(4): Show | 7 | HG01109.hp1 HG01109.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1906+4307_1906+430 others(7): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | INFO_REALIGN_3_PRIME | chr1 | 15333824 | |||||
| chr1:15333824
|
C | CTTTT | 6 | a0001c0032t0023g0282a0003c0085t0055g0139a0004c0087t0046g0121others(3): Show | 6 | HG02717.hp1 HG02965.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1906+4306_1906+430 others(8): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | INFO_REALIGN_3_PRIME | chr1 | 15333824 | |||||
| chr1:15333824
|
C | T | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1906+4283C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15333824 | ||||||
| chr1:15333824
|
CT | C | 64 | a0001c0001t0002g0054a0001c0001t0002g0070a0001c0001t0002g0093others(61): Show | 64 | HG00735.hp1 HG01070.hp1 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.1906+4309delT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | INFO_REALIGN_3_PRIME | chr1 | 15333824 | |||||
| chr1:15333824
|
CTTT | C | 8 | a0007c0012t0026g0245a0007c0012t0026g0246a0024c0027t0024g0258others(5): Show | 8 | HG01243.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1906+4307_1906+430 others(7): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | INFO_REALIGN_3_PRIME | chr1 | 15333824 | |||||
| chr1:15333824
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0001g0063 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1906+4300_1906+430 others(14): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | INFO_REALIGN_3_PRIME | chr1 | 15333824 | |||||
| chr1:15333977
|
C | T | 4 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241others(1): Show | 4 | HG02965.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1906+4436C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15333977 | ||||||
| chr1:15334029
|
G | A | 4 | a0003c0086t0009g0142a0005c0070t0035g0287a0046c0078t0007g0232others(1): Show | 4 | HG01070.hp1 HG02280.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1906+4488G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15334029 | ||||||
| chr1:15334067
|
A | G | 5 | a0001c0032t0023g0282a0003c0085t0055g0139a0004c0087t0046g0121others(2): Show | 5 | HG02717.hp1 HG02965.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1906+4526A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15334067 | ||||||
| chr1:15334085
|
C | T | 2 | a0023c0127t0019g0184a0039c0126t0019g0185 | 2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1906+4544C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15334085 | ||||||
| chr1:15334118
|
G | A | 1 | a0001c0002t0001g0061 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1906+4577G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15334118 | ||||||
| chr1:15334133
|
G | T | 91 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0013t0001g0045others(88): Show | 91 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.1906+4592G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15334133 | ||||||
| chr1:15334153
|
C | T | 15 | a0002c0018t0007g0140a0014c0110t0008g0254a0018c0020t0022g0239others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1906+4612C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15334153 | ||||||
| chr1:15334177
|
A | G | 88 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0013t0001g0045others(85): Show | 88 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(85): Show |
intron_variant | MODIFIER | c.1906+4636A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15334177 | ||||||
| chr1:15334236
|
C | A | 5 | a0001c0032t0023g0282a0003c0085t0055g0139a0004c0087t0046g0121others(2): Show | 5 | HG02717.hp1 HG02965.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1906+4695C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15334236 | ||||||
| chr1:15334561
|
C | T | 1 | a0002c0019t0027g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1907-4920C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15334561 | ||||||
| chr1:15334603
|
G | A | 2 | a0003c0006t0008g0171a0004c0004t0005g0174 | 2 | HG02523.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1907-4878G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15334603 | ||||||
| chr1:15334661
|
G | A | 2 | a0001c0102t0012g0146a0004c0038t0014g0155 | 2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1907-4820G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15334661 | ||||||
| chr1:15334744
|
G | A | 1 | a0004c0004t0004g0086 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1907-4737G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15334744 | ||||||
| chr1:15334808
|
C | T | 78 | a0001c0013t0001g0045a0001c0013t0001g0051a0001c0013t0001g0053others(75): Show | 78 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.1907-4673C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15334808 | ||||||
| chr1:15335040
|
C | T | 2 | a0022c0046t0009g0222a0039c0126t0019g0185 | 2 | HG02132.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1907-4441C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15335040 | ||||||
| chr1:15335074
|
C | T | 2 | a0004c0087t0046g0121a0007c0033t0014g0068 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1907-4407C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15335074 | ||||||
| chr1:15335339
|
T | C | 5 | a0001c0032t0023g0282a0003c0085t0055g0139a0004c0087t0046g0121others(2): Show | 5 | HG02717.hp1 HG02965.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1907-4142T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15335339 | ||||||
| chr1:15335469
|
C | T | 1 | a0004c0058t0006g0183 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1907-4012C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15335469 | ||||||
| chr1:15335478
|
CT | C | 21 | a0001c0032t0023g0282a0002c0019t0027g0244a0002c0080t0019g0181others(18): Show | 21 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1907-3990delT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | INFO_REALIGN_3_PRIME | chr1 | 15335478 | |||||
| chr1:15335491
|
T | A | 1 | a0004c0096t0002g0033 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1907-3990T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15335491 | ||||||
| chr1:15335713
|
A | G | 1 | a0002c0003t0014g0151 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1907-3768A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15335713 | ||||||
| chr1:15335757
|
T | C | 2 | a0012c0079t0027g0248a0059c0104t0045g0014 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1907-3724T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15335757 | ||||||
| chr1:15336079
|
C | T | 1 | a0009c0028t0011g0290 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1907-3402C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15336079 | ||||||
| chr1:15336110
|
C | T | 29 | a0001c0013t0001g0045a0001c0013t0001g0051a0001c0013t0001g0053others(26): Show | 29 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1907-3371C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15336110 | ||||||
| chr1:15336168
|
C | G | 3 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241 | 3 | HG02965.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1907-3313C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15336168 | ||||||
| chr1:15336297
|
A | G | 1 | a0012c0079t0027g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1907-3184A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15336297 | ||||||
| chr1:15336304
|
CTAT | C | 6 | a0002c0080t0019g0181a0002c0081t0058g0251a0004c0087t0046g0121others(3): Show | 6 | HG02896.hp1 HG02922.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1907-3170_1907-316 others(7): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | INFO_REALIGN_3_PRIME | chr1 | 15336304 | |||||
| chr1:15336469
|
C | A | 5 | a0001c0032t0023g0282a0002c0019t0027g0244a0003c0085t0055g0139others(2): Show | 5 | HG02572.hp2 HG02717.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1907-3012C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15336469 | ||||||
| chr1:15336612
|
C | A | 1 | a0003c0006t0013g0060 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1907-2869C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15336612 | ||||||
| chr1:15336635
|
G | A | 1 | a0039c0126t0019g0185 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1907-2846G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15336635 | ||||||
| chr1:15336679
|
T | C | 1 | a0005c0070t0035g0287 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1907-2802T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15336679 | ||||||
| chr1:15336888
|
A | G | 45 | a0001c0001t0057g0250a0001c0010t0001g0182a0001c0032t0014g0152others(42): Show | 45 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.1907-2593A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15336888 | ||||||
| chr1:15336935
|
T | C | 30 | a0001c0013t0001g0045a0001c0013t0001g0051a0001c0013t0001g0053others(27): Show | 30 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1907-2546T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15336935 | ||||||
| chr1:15337191
|
G | A | 12 | a0014c0110t0008g0254a0016c0107t0003g0145a0018c0020t0022g0239others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1907-2290G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15337191 | ||||||
| chr1:15337270
|
C | G | 2 | a0021c0117t0016g0234a0063c0067t0039g0004 | 2 | HG01099.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1907-2211C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15337270 | ||||||
| chr1:15337366
|
C | T | 2 | a0001c0010t0001g0097a0001c0010t0001g0098 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1907-2115C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15337366 | ||||||
| chr1:15337368
|
C | G | 1 | a0002c0019t0027g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1907-2113C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15337368 | ||||||
| chr1:15337418
|
CAGTT | C | 3 | a0025c0042t0003g0010a0025c0042t0003g0011a0062c0062t0011g0285 | 3 | HG01069.hp1 HG01071.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1907-2060_1907-205 others(8): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | INFO_REALIGN_3_PRIME | chr1 | 15337418 | |||||
| chr1:15337448
|
C | T | 14 | a0002c0018t0018g0153a0007c0012t0016g0187a0012c0041t0003g0124others(11): Show | 14 | HG01109.hp2 HG01255.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.1907-2033C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15337448 | ||||||
| chr1:15337466
|
C | T | 2 | a0003c0055t0012g0213a0004c0004t0004g0168 | 2 | HG00423.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1907-2015C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15337466 | ||||||
| chr1:15337532
|
G | A | 1 | a0039c0126t0019g0185 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1907-1949G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15337532 | ||||||
| chr1:15337561
|
G | A | 1 | a0002c0003t0004g0044 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1907-1920G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15337561 | ||||||
| chr1:15337851
|
C | A | 15 | a0002c0018t0018g0153a0007c0012t0016g0187a0012c0041t0003g0124others(12): Show | 15 | HG01109.hp2 HG01255.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.1907-1630C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15337851 | ||||||
| chr1:15337914
|
C | T | 4 | a0001c0001t0012g0126a0001c0008t0012g0205a0009c0028t0011g0290others(1): Show | 4 | HG01074.hp2 HG02683.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1907-1567C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15337914 | ||||||
| chr1:15338015
|
C | T | 3 | a0004c0038t0007g0143a0028c0109t0007g0197a0031c0119t0009g0257 | 3 | HG01884.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1907-1466C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15338015 | ||||||
| chr1:15338206
|
G | T | 2 | a0037c0128t0007g0233a0038c0129t0007g0235 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1907-1275G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15338206 | ||||||
| chr1:15338280
|
C | T | 1 | a0002c0019t0027g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1907-1201C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15338280 | ||||||
| chr1:15338478
|
T | A | 1 | a0001c0002t0001g0058 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1907-1003T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15338478 | ||||||
| chr1:15338564
|
G | A | 2 | a0003c0006t0002g0018a0008c0044t0009g0223 | 2 | HG00544.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1907-917G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15338564 | ||||||
| chr1:15338904
|
C | T | 2 | a0037c0128t0007g0233a0038c0129t0007g0235 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1907-577C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15338904 | ||||||
| chr1:15339063
|
C | T | 5 | a0001c0032t0014g0152a0003c0086t0009g0142a0005c0070t0035g0287others(2): Show | 5 | HG01070.hp1 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1907-418C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15339063 | ||||||
| chr1:15339273
|
A | G | 10 | a0001c0032t0014g0152a0001c0032t0023g0282a0002c0019t0027g0244others(7): Show | 10 | HG01070.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1907-208A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15339273 | ||||||
| chr1:15339306
|
C | G | 1 | a0062c0062t0011g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1907-175C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15339306 | ||||||
| chr1:15339387
|
T | C | 1 | a0022c0046t0009g0193 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1907-94T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15339387 | ||||||
| chr1:15339424
|
C | T | 1 | a0001c0002t0001g0188 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1907-57C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15339424 | ||||||
| chr1:15339446
|
G | T | 9 | a0014c0110t0008g0254a0016c0107t0003g0145a0020c0111t0030g0179others(6): Show | 9 | HG01069.hp1 HG01071.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1907-35G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 14/33 | chr1 | 15339446 | ||||||
| chr1:15339589
|
C | T | 1 | a0001c0008t0008g0204 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1977+38C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15339589 | ||||||
| chr1:15339597
|
G | C | 3 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241 | 3 | HG02965.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1977+46G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15339597 | ||||||
| chr1:15339659
|
C | G | 8 | a0001c0001t0002g0081a0001c0108t0001g0165a0002c0003t0053g0176others(5): Show | 8 | HG00673.hp1 NA18950.hp2 NA18984.hp2 others(5): Show |
intron_variant | MODIFIER | c.1977+108C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15339659 | ||||||
| chr1:15339672
|
T | C | 2 | a0037c0128t0007g0233a0038c0129t0007g0235 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1977+121T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15339672 | ||||||
| chr1:15339751
|
T | C | 5 | a0001c0001t0002g0040a0001c0001t0002g0070a0001c0001t0014g0052others(2): Show | 5 | HG01361.hp2 HG01952.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1977+200T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15339751 | ||||||
| chr1:15339837
|
A | AT | 7 | a0001c0032t0014g0152a0003c0086t0009g0142a0005c0070t0035g0287others(4): Show | 7 | HG01070.hp1 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1977+298dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | INFO_REALIGN_3_PRIME | chr1 | 15339837 | |||||
| chr1:15339918
|
C | T | 1 | a0006c0014t0005g0255 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1977+367C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15339918 | ||||||
| chr1:15339919
|
G | A | 1 | a0012c0097t0003g0141 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1977+368G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15339919 | ||||||
| chr1:15340124
|
C | G | 13 | a0001c0032t0014g0152a0001c0032t0023g0282a0002c0019t0027g0244others(10): Show | 13 | HG01070.hp1 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1977+573C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15340124 | ||||||
| chr1:15340138
|
A | G | 6 | a0002c0018t0007g0140a0002c0018t0021g0247a0014c0112t0007g0202others(3): Show | 6 | HG02630.hp1 HG02723.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1977+587A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15340138 | ||||||
| chr1:15340187
|
A | G | 1 | a0009c0011t0017g0294 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1977+636A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15340187 | ||||||
| chr1:15340292
|
A | G | 1 | a0002c0018t0018g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1977+741A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15340292 | ||||||
| chr1:15340368
|
G | A | 3 | a0012c0041t0003g0124a0012c0041t0003g0125a0012c0051t0011g0284 | 3 | HG01255.hp2 HG01261.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1977+817G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15340368 | ||||||
| chr1:15340415
|
T | C | 6 | a0001c0090t0048g0158a0002c0003t0014g0151a0002c0080t0019g0181others(3): Show | 6 | HG02055.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1977+864T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15340415 | ||||||
| chr1:15340642
|
G | A | 1 | a0039c0126t0019g0185 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1977+1091G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15340642 | ||||||
| chr1:15340650
|
C | G | 3 | a0026c0031t0003g0252a0026c0031t0003g0253a0043c0068t0011g0292 | 3 | HG02055.hp2 HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1978-1086C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15340650 | ||||||
| chr1:15340763
|
A | G | 8 | a0001c0001t0002g0081a0001c0108t0001g0165a0002c0003t0053g0176others(5): Show | 8 | HG00673.hp1 NA18950.hp2 NA18984.hp2 others(5): Show |
intron_variant | MODIFIER | c.1978-973A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15340763 | ||||||
| chr1:15340811
|
C | T | 6 | a0014c0110t0008g0254a0016c0107t0003g0145a0025c0042t0003g0010others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1978-925C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15340811 | ||||||
| chr1:15340947
|
T | C | 49 | a0001c0032t0014g0152a0001c0032t0023g0282a0002c0018t0007g0140others(46): Show | 49 | HG01069.hp1 HG01070.hp1 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.1978-789T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15340947 | ||||||
| chr1:15341106
|
C | T | 2 | a0037c0128t0007g0233a0038c0129t0007g0235 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1978-630C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15341106 | ||||||
| chr1:15341185
|
A | C | 1 | a0007c0012t0016g0187 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1978-551A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15341185 | ||||||
| chr1:15341190
|
C | A | 6 | a0001c0015t0001g0109a0001c0015t0001g0110a0001c0015t0001g0111others(3): Show | 6 | HG01123.hp2 HG01192.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.1978-546C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15341190 | ||||||
| chr1:15341240
|
G | T | 1 | a0037c0128t0007g0233 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1978-496G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15341240 | ||||||
| chr1:15341282
|
C | A | 4 | a0014c0110t0008g0254a0025c0042t0003g0010a0025c0042t0003g0011others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1978-454C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15341282 | ||||||
| chr1:15341382
|
G | A | 2 | a0029c0114t0056g0199a0030c0115t0054g0203 | 2 | HG01167.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1978-354G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15341382 | ||||||
| chr1:15341438
|
C | T | 10 | a0001c0032t0014g0152a0001c0032t0023g0282a0002c0019t0027g0244others(7): Show | 10 | HG01070.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1978-298C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 15/33 | chr1 | 15341438 | ||||||
| chr1:15342086
|
A | C | 6 | a0002c0018t0007g0140a0002c0018t0021g0247a0014c0112t0007g0202others(3): Show | 6 | HG02630.hp1 HG02723.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2130+198A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15342086 | ||||||
| chr1:15342135
|
G | A | 27 | a0001c0013t0001g0045a0001c0013t0001g0051a0001c0013t0001g0053others(24): Show | 27 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.2130+247G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15342135 | ||||||
| chr1:15342202
|
G | A | 1 | a0001c0015t0001g0109 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2130+314G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15342202 | ||||||
| chr1:15342203
|
A | G | 2 | a0002c0018t0018g0153a0004c0038t0014g0155 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2130+315A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15342203 | ||||||
| chr1:15342302
|
A | G | 3 | a0004c0004t0004g0024a0004c0004t0004g0027a0011c0034t0006g0085 | 3 | NA18944.hp1 NA18978.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.2130+414A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15342302 | ||||||
| chr1:15342319
|
T | C | 49 | a0001c0032t0014g0152a0001c0032t0023g0282a0002c0018t0007g0140others(46): Show | 49 | HG01069.hp1 HG01070.hp1 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.2130+431T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15342319 | ||||||
| chr1:15342421
|
C | T | 1 | a0056c0103t0051g0243 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2130+533C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15342421 | ||||||
| chr1:15342464
|
G | A | 6 | a0002c0080t0019g0181a0002c0081t0058g0251a0004c0087t0046g0121others(3): Show | 6 | HG02896.hp1 HG02922.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.2130+576G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15342464 | ||||||
| chr1:15342678
|
A | G | 1 | a0002c0081t0058g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2130+790A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15342678 | ||||||
| chr1:15342737
|
A | G | 78 | a0001c0013t0001g0045a0001c0013t0001g0051a0001c0013t0001g0053others(75): Show | 78 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.2130+849A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15342737 | ||||||
| chr1:15342892
|
C | A | 1 | a0007c0012t0016g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2130+1004C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15342892 | ||||||
| chr1:15343180
|
A | G | 1 | a0009c0011t0019g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2130+1292A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15343180 | ||||||
| chr1:15343275
|
G | A | 4 | a0001c0032t0023g0282a0003c0085t0055g0139a0007c0033t0007g0138others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2130+1387G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15343275 | ||||||
| chr1:15343390
|
C | T | 2 | a0037c0128t0007g0233a0038c0129t0007g0235 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2130+1502C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15343390 | ||||||
| chr1:15343512
|
T | G | 4 | a0001c0090t0048g0158a0002c0003t0014g0151a0006c0014t0005g0255others(1): Show | 4 | HG00642.hp2 HG02055.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2131-1571T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15343512 | ||||||
| chr1:15343673
|
A | G | 2 | a0002c0035t0006g0026a0050c0093t0018g0020 | 2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2131-1410A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15343673 | ||||||
| chr1:15343948
|
G | A | 1 | a0002c0003t0005g0172 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2131-1135G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15343948 | ||||||
| chr1:15343949
|
C | T | 1 | a0045c0075t0010g0278 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2131-1134C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15343949 | ||||||
| chr1:15344079
|
G | A | 1 | a0003c0098t0029g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2131-1004G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15344079 | ||||||
| chr1:15344098
|
TGC | T | 13 | a0001c0032t0014g0152a0001c0032t0023g0282a0002c0019t0027g0244others(10): Show | 13 | HG01070.hp1 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.2131-984_2131-983d others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15344098 | ||||||
| chr1:15344160
|
A | G | 2 | a0002c0003t0006g0069a0004c0096t0002g0033 | 2 | HG02135.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2131-923A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15344160 | ||||||
| chr1:15344343
|
C | A | 2 | a0006c0014t0005g0255a0007c0012t0016g0187 | 2 | HG00642.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2131-740C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15344343 | ||||||
| chr1:15344365
|
C | T | 1 | a0002c0035t0006g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2131-718C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15344365 | ||||||
| chr1:15344417
|
A | T | 5 | a0001c0001t0002g0081a0001c0108t0001g0165a0002c0003t0053g0176others(2): Show | 5 | NA18984.hp2 NA18991.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.2131-666A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15344417 | ||||||
| chr1:15344484
|
T | G | 14 | a0001c0032t0014g0152a0001c0032t0023g0282a0002c0019t0027g0244others(11): Show | 14 | HG01070.hp1 HG02280.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.2131-599T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15344484 | ||||||
| chr1:15344905
|
G | GCTCTACC others(6): Show |
1 | a0066c0061t0042g0007 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2131-174_2131-162d others(15): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | INFO_REALIGN_3_PRIME | chr1 | 15344905 | |||||
| chr1:15344987
|
G | A | 151 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0054others(148): Show | 151 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.2131-96G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 16/33 | chr1 | 15344987 | ||||||
| chr1:15345199
|
C | T | 1 | a0015c0023t0008g0131 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2238+9C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 17/33 | chr1 | 15345199 | ||||||
| chr1:15345202
|
A | G | 1 | a0028c0109t0007g0197 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2238+12A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 17/33 | chr1 | 15345202 | ||||||
| chr1:15345284
|
T | G | 1 | a0012c0079t0027g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2238+94T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 17/33 | chr1 | 15345284 | ||||||
| chr1:15345560
|
C | T | 1 | a0001c0002t0001g0102 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2346+37C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15345560 | ||||||
| chr1:15345577
|
G | A | 9 | a0014c0110t0008g0254a0016c0107t0003g0145a0020c0111t0030g0179others(6): Show | 9 | HG01069.hp1 HG01071.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2346+54G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15345577 | ||||||
| chr1:15345594
|
G | A | 1 | a0018c0020t0022g0241 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2346+71G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15345594 | ||||||
| chr1:15345721
|
T | C | 1 | a0011c0034t0006g0085 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2346+198T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15345721 | ||||||
| chr1:15345797
|
T | G | 4 | a0017c0017t0007g0008a0017c0017t0007g0147a0017c0017t0007g0148others(1): Show | 4 | HG02257.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2346+274T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15345797 | ||||||
| chr1:15345864
|
G | A | 3 | a0002c0019t0006g0066a0006c0045t0003g0225a0011c0099t0006g0087 | 3 | HG00558.hp1 NA18612.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.2346+341G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15345864 | ||||||
| chr1:15345945
|
T | C | 82 | a0001c0001t0002g0040a0001c0001t0002g0057a0001c0001t0002g0070others(79): Show | 82 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.2346+422T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15345945 | ||||||
| chr1:15345950
|
G | C | 2 | a0001c0039t0001g0036a0001c0039t0001g0037 | 2 | HG03017.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.2346+427G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15345950 | ||||||
| chr1:15346418
|
C | T | 1 | a0001c0008t0012g0205 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2346+895C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15346418 | ||||||
| chr1:15346479
|
C | T | 4 | a0002c0019t0027g0244a0026c0031t0003g0252a0026c0031t0003g0253others(1): Show | 4 | HG02055.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2346+956C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15346479 | ||||||
| chr1:15346480
|
G | A | 6 | a0001c0032t0014g0152a0003c0086t0009g0142a0004c0038t0014g0155others(3): Show | 6 | HG01070.hp1 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2346+957G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15346480 | ||||||
| chr1:15346850
|
C | T | 1 | a0001c0013t0001g0045 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2346+1327C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15346850 | ||||||
| chr1:15346868
|
T | C | 4 | a0004c0004t0005g0174a0019c0022t0004g0022a0019c0022t0004g0071others(1): Show | 4 | HG02132.hp1 NA18950.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.2346+1345T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15346868 | ||||||
| chr1:15346907
|
G | A | 1 | a0033c0131t0005g0219 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2346+1384G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15346907 | ||||||
| chr1:15347193
|
G | A | 1 | a0004c0087t0046g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2346+1670G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15347193 | ||||||
| chr1:15347275
|
T | C | 3 | a0001c0001t0057g0250a0002c0035t0006g0026a0050c0093t0018g0020 | 3 | HG02280.hp1 HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2346+1752T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15347275 | ||||||
| chr1:15347292
|
A | C | 1 | a0005c0072t0010g0270 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2347-1750A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15347292 | ||||||
| chr1:15347631
|
T | C | 18 | a0001c0001t0013g0104a0001c0002t0018g0156a0001c0002t0049g0101others(15): Show | 18 | HG00642.hp2 HG00735.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.2347-1411T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15347631 | ||||||
| chr1:15347767
|
A | T | 1 | a0002c0019t0027g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2347-1275A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15347767 | ||||||
| chr1:15347772
|
C | T | 12 | a0001c0032t0023g0282a0002c0018t0018g0153a0002c0019t0027g0244others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2347-1270C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15347772 | ||||||
| chr1:15347773
|
C | T | 12 | a0007c0012t0026g0245a0007c0012t0026g0246a0018c0020t0022g0239others(9): Show | 12 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2347-1269C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15347773 | ||||||
| chr1:15347814
|
G | T | 1 | a0001c0001t0008g0160 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2347-1228G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15347814 | ||||||
| chr1:15347901
|
C | T | 1 | a0002c0003t0004g0017 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2347-1141C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15347901 | ||||||
| chr1:15348019
|
C | T | 1 | a0054c0084t0047g0154 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2347-1023C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15348019 | ||||||
| chr1:15348698
|
C | G | 2 | a0002c0035t0006g0026a0050c0093t0018g0020 | 2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2347-344C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15348698 | ||||||
| chr1:15348707
|
C | A | 2 | a0001c0010t0001g0097a0001c0010t0001g0098 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2347-335C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15348707 | ||||||
| chr1:15348708
|
G | A | 1 | a0007c0101t0014g0119 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2347-334G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15348708 | ||||||
| chr1:15348743
|
T | G | 12 | a0001c0001t0013g0104a0001c0002t0018g0156a0001c0002t0049g0101others(9): Show | 12 | HG00735.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2347-299T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15348743 | ||||||
| chr1:15348745
|
C | T | 3 | a0006c0014t0005g0255a0007c0012t0016g0187a0021c0113t0016g0194 | 3 | HG00642.hp2 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2347-297C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15348745 | ||||||
| chr1:15348756
|
G | A | 10 | a0001c0032t0014g0152a0004c0038t0007g0143a0004c0087t0046g0121others(7): Show | 10 | HG01884.hp2 HG02280.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2347-286G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15348756 | ||||||
| chr1:15348823
|
T | A | 1 | a0059c0104t0045g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2347-219T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 18/33 | chr1 | 15348823 | ||||||
| chr1:15349225
|
C | T | 12 | a0001c0001t0013g0104a0001c0002t0018g0156a0001c0002t0049g0101others(9): Show | 12 | HG00735.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2454+76C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15349225 | ||||||
| chr1:15349404
|
T | C | 3 | a0014c0110t0008g0254a0023c0130t0007g0238a0064c0063t0030g0195 | 3 | HG01109.hp2 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2454+255T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15349404 | ||||||
| chr1:15349541
|
T | C | 4 | a0017c0017t0007g0008a0017c0017t0007g0147a0017c0017t0007g0148others(1): Show | 4 | HG02257.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2454+392T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15349541 | ||||||
| chr1:15349554
|
G | A | 129 | a0001c0001t0002g0049a0001c0001t0002g0057a0001c0001t0012g0128others(126): Show | 129 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.2454+405G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15349554 | ||||||
| chr1:15349589
|
G | A | 1 | a0002c0003t0004g0017 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2454+440G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15349589 | ||||||
| chr1:15349623
|
G | A | 1 | a0001c0002t0031g0088 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2454+474G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15349623 | ||||||
| chr1:15349939
|
C | A | 3 | a0005c0005t0015g0283a0008c0122t0009g0215a0009c0011t0017g0294 | 3 | HG00609.hp1 NA18966.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2454+790C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15349939 | ||||||
| chr1:15349961
|
G | A | 2 | a0001c0090t0048g0158a0002c0003t0014g0151 | 2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2454+812G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15349961 | ||||||
| chr1:15350007
|
G | A | 85 | a0001c0001t0002g0049a0001c0001t0002g0057a0001c0001t0012g0128others(82): Show | 85 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.2454+858G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15350007 | ||||||
| chr1:15350013
|
C | T | 1 | a0019c0022t0018g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2454+864C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15350013 | ||||||
| chr1:15350035
|
A | G | 3 | a0016c0107t0003g0145a0023c0127t0019g0184a0041c0076t0038g0289 | 3 | HG02145.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2454+886A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15350035 | ||||||
| chr1:15350041
|
G | A | 12 | a0001c0001t0013g0104a0001c0002t0018g0156a0001c0002t0049g0101others(9): Show | 12 | HG00735.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2454+892G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15350041 | ||||||
| chr1:15350090
|
C | T | 2 | a0004c0004t0004g0029a0004c0004t0004g0030 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2454+941C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15350090 | ||||||
| chr1:15350090
|
CGGTTCGA others(4): Show |
C | 1 | a0016c0107t0003g0145 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2454+943_2454+953d others(13): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | INFO_REALIGN_3_PRIME | chr1 | 15350090 | |||||
| chr1:15350101
|
G | A | 1 | a0064c0063t0030g0195 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2454+952G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15350101 | ||||||
| chr1:15350103
|
T | A | 1 | a0016c0107t0003g0145 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2454+954T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15350103 | ||||||
| chr1:15350114
|
C | T | 1 | a0054c0084t0047g0154 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2454+965C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15350114 | ||||||
| chr1:15350115
|
G | A | 3 | a0016c0107t0003g0145a0023c0127t0019g0184a0041c0076t0038g0289 | 3 | HG02145.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2454+966G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15350115 | ||||||
| chr1:15350119
|
A | G | 1 | a0012c0097t0003g0141 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2454+970A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15350119 | ||||||
| chr1:15350127
|
T | C | 5 | a0002c0018t0018g0153a0017c0017t0007g0008a0017c0017t0007g0147others(2): Show | 5 | HG02257.hp1 HG02486.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2454+978T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15350127 | ||||||
| chr1:15350289
|
C | T | 24 | a0001c0001t0013g0104a0001c0002t0018g0156a0001c0002t0049g0101others(21): Show | 24 | HG00735.hp2 HG01167.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.2454+1140C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15350289 | ||||||
| chr1:15350305
|
A | G | 7 | a0001c0010t0001g0182a0001c0090t0048g0158a0002c0003t0014g0151others(4): Show | 7 | HG02055.hp1 HG02717.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2454+1156A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15350305 | ||||||
| chr1:15350313
|
G | A | 3 | a0016c0107t0003g0145a0023c0127t0019g0184a0041c0076t0038g0289 | 3 | HG02145.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2454+1164G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15350313 | ||||||
| chr1:15350388
|
A | C | 1 | a0001c0002t0001g0063 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2454+1239A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15350388 | ||||||
| chr1:15350402
|
G | T | 1 | a0059c0104t0045g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2454+1253G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15350402 | ||||||
| chr1:15350570
|
A | G | 128 | a0001c0001t0002g0049a0001c0001t0002g0057a0001c0001t0012g0128others(125): Show | 128 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.2454+1421A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15350570 | ||||||
| chr1:15350665
|
A | G | 129 | a0001c0001t0002g0049a0001c0001t0002g0057a0001c0001t0012g0128others(126): Show | 129 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.2454+1516A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15350665 | ||||||
| chr1:15351066
|
T | C | 1 | a0048c0091t0009g0132 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2455-1811T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15351066 | ||||||
| chr1:15351197
|
T | C | 8 | a0001c0032t0014g0152a0003c0086t0009g0142a0004c0038t0007g0143others(5): Show | 8 | HG01070.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2455-1680T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15351197 | ||||||
| chr1:15351237
|
C | T | 1 | a0020c0111t0030g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2455-1640C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15351237 | ||||||
| chr1:15351373
|
T | A | 90 | a0001c0001t0002g0049a0001c0001t0002g0057a0001c0001t0012g0128others(87): Show | 90 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.2455-1504T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15351373 | ||||||
| chr1:15351374
|
T | A | 1 | a0007c0033t0007g0138 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2455-1503T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15351374 | ||||||
| chr1:15351385
|
G | T | 2 | a0001c0008t0025g0112a0001c0008t0025g0113 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2455-1492G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15351385 | ||||||
| chr1:15351436
|
A | G | 128 | a0001c0001t0002g0049a0001c0001t0002g0057a0001c0001t0012g0128others(125): Show | 128 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.2455-1441A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15351436 | ||||||
| chr1:15351487
|
T | G | 10 | a0001c0001t0002g0049a0001c0002t0001g0019a0002c0003t0006g0062others(7): Show | 10 | HG00423.hp2 HG00621.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.2455-1390T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15351487 | ||||||
| chr1:15351500
|
C | G | 1 | a0007c0033t0014g0068 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2455-1377C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15351500 | ||||||
| chr1:15351656
|
A | C | 12 | a0007c0012t0026g0245a0007c0012t0026g0246a0018c0020t0022g0239others(9): Show | 12 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2455-1221A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15351656 | ||||||
| chr1:15351860
|
G | A | 24 | a0001c0001t0013g0104a0001c0002t0018g0156a0001c0002t0049g0101others(21): Show | 24 | HG00735.hp2 HG01167.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.2455-1017G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15351860 | ||||||
| chr1:15352145
|
T | G | 8 | a0001c0032t0014g0152a0003c0086t0009g0142a0004c0038t0007g0143others(5): Show | 8 | HG01070.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2455-732T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15352145 | ||||||
| chr1:15352261
|
A | G | 1 | a0020c0111t0030g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2455-616A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15352261 | ||||||
| chr1:15352554
|
A | G | 8 | a0001c0032t0014g0152a0003c0086t0009g0142a0004c0038t0007g0143others(5): Show | 8 | HG01070.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2455-323A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15352554 | ||||||
| chr1:15352858
|
C | T | 1 | a0009c0011t0019g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2455-19C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 19/33 | chr1 | 15352858 | ||||||
| chr1:15352987
|
A | G | 2 | a0001c0002t0001g0079a0002c0007t0003g0186 | 2 | NA18956.hp1 NA18956.hp2 |
splice_region_variant&intron_variant | LOW | c.2562+3A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15352987 | ||||||
| chr1:15353342
|
A | G | 2 | a0001c0039t0001g0036a0001c0039t0001g0037 | 2 | HG03017.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.2562+358A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15353342 | ||||||
| chr1:15353417
|
G | A | 8 | a0001c0032t0014g0152a0003c0086t0009g0142a0004c0038t0007g0143others(5): Show | 8 | HG01070.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2562+433G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15353417 | ||||||
| chr1:15353435
|
T | A | 1 | a0001c0002t0001g0023 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2562+451T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15353435 | ||||||
| chr1:15353453
|
C | G | 12 | a0001c0001t0013g0104a0001c0002t0018g0156a0001c0002t0049g0101others(9): Show | 12 | HG00735.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2562+469C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15353453 | ||||||
| chr1:15353636
|
C | A | 4 | a0012c0079t0027g0248a0016c0107t0003g0145a0023c0127t0019g0184others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2562+652C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15353636 | ||||||
| chr1:15353704
|
C | CA | 18 | a0001c0001t0002g0093a0001c0001t0013g0048a0001c0001t0057g0250others(15): Show | 18 | HG01070.hp1 HG01361.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.2562+742dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15353704 | |||||
| chr1:15353704
|
CA | C | 64 | a0001c0001t0002g0049a0001c0001t0002g0057a0001c0001t0012g0128others(61): Show | 64 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.2562+742delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15353704 | |||||
| chr1:15353704
|
CAA | C | 29 | a0001c0001t0013g0104a0001c0002t0018g0156a0001c0002t0049g0101others(26): Show | 29 | HG00735.hp2 HG01074.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.2562+741_2562+742d others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15353704 | |||||
| chr1:15353724
|
AAAG | A | 7 | a0001c0010t0001g0182a0001c0090t0048g0158a0002c0003t0014g0151others(4): Show | 7 | HG02055.hp1 HG02717.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2562+743_2562+745d others(5): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15353724 | |||||
| chr1:15353726
|
A | G | 1 | a0002c0018t0018g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2562+742A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15353726 | ||||||
| chr1:15353732
|
G | GA | 12 | a0007c0012t0026g0245a0007c0012t0026g0246a0018c0020t0022g0239others(9): Show | 12 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2562+761dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15353732 | |||||
| chr1:15353732
|
GA | G | 15 | a0001c0001t0013g0104a0001c0002t0018g0156a0001c0002t0049g0101others(12): Show | 15 | HG00735.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.2562+761delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15353732 | |||||
| chr1:15353878
|
C | G | 1 | a0020c0111t0030g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2562+894C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15353878 | ||||||
| chr1:15353905
|
A | G | 1 | a0001c0001t0012g0128 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2562+921A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15353905 | ||||||
| chr1:15353906
|
C | T | 8 | a0001c0032t0014g0152a0003c0086t0009g0142a0004c0038t0007g0143others(5): Show | 8 | HG01070.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2562+922C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15353906 | ||||||
| chr1:15353955
|
G | T | 129 | a0001c0001t0002g0049a0001c0001t0002g0057a0001c0001t0012g0128others(126): Show | 129 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.2562+971G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15353955 | ||||||
| chr1:15354040
|
A | G | 4 | a0012c0079t0027g0248a0016c0107t0003g0145a0023c0127t0019g0184others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2562+1056A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15354040 | ||||||
| chr1:15354525
|
G | A | 12 | a0001c0001t0013g0104a0001c0002t0018g0156a0001c0002t0049g0101others(9): Show | 12 | HG00735.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2562+1541G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15354525 | ||||||
| chr1:15354634
|
T | C | 1 | a0012c0097t0003g0141 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2562+1650T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15354634 | ||||||
| chr1:15354676
|
GA | G | 12 | a0007c0012t0026g0245a0007c0012t0026g0246a0018c0020t0022g0239others(9): Show | 12 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2562+1702delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15354676 | |||||
| chr1:15354701
|
C | A | 2 | a0012c0041t0003g0124a0012c0041t0003g0125 | 2 | HG01255.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.2562+1717C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15354701 | ||||||
| chr1:15354875
|
G | A | 12 | a0007c0012t0026g0245a0007c0012t0026g0246a0018c0020t0022g0239others(9): Show | 12 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2562+1891G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15354875 | ||||||
| chr1:15354893
|
T | C | 90 | a0001c0001t0002g0049a0001c0001t0002g0057a0001c0001t0012g0128others(87): Show | 90 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.2562+1909T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15354893 | ||||||
| chr1:15354938
|
G | A | 11 | a0001c0001t0013g0104a0001c0002t0018g0156a0001c0002t0049g0101others(8): Show | 11 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2562+1954G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15354938 | ||||||
| chr1:15354944
|
C | CA | 91 | a0001c0001t0002g0049a0001c0001t0002g0057a0001c0001t0012g0128others(88): Show | 91 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.2562+1961dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15354944 | |||||
| chr1:15355134
|
G | A | 1 | a0001c0001t0012g0126 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2562+2150G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15355134 | ||||||
| chr1:15355137
|
A | C | 70 | a0001c0001t0002g0049a0001c0001t0002g0057a0001c0001t0012g0128others(67): Show | 70 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.2562+2153A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15355137 | ||||||
| chr1:15355170
|
T | C | 1 | a0004c0058t0006g0183 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2562+2186T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15355170 | ||||||
| chr1:15355208
|
C | CA | 25 | a0001c0001t0013g0104a0001c0002t0018g0156a0001c0002t0049g0101others(22): Show | 25 | HG00735.hp2 HG01167.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.2562+2239dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15355208 | |||||
| chr1:15355208
|
CA | C | 10 | a0001c0002t0001g0038a0001c0010t0001g0182a0001c0090t0048g0158others(7): Show | 10 | HG02055.hp1 HG02572.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.2562+2239delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15355208 | |||||
| chr1:15355448
|
G | C | 28 | a0001c0001t0013g0104a0001c0002t0018g0156a0001c0002t0049g0101others(25): Show | 28 | HG00735.hp2 HG01167.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.2562+2464G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15355448 | ||||||
| chr1:15355455
|
G | A | 1 | a0002c0018t0021g0247 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2562+2471G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15355455 | ||||||
| chr1:15355612
|
G | A | 1 | a0007c0033t0014g0068 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2563-2498G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15355612 | ||||||
| chr1:15355794
|
C | T | 1 | a0005c0016t0032g0260 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2563-2316C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15355794 | ||||||
| chr1:15355831
|
G | A | 1 | a0004c0038t0014g0155 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2563-2279G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15355831 | ||||||
| chr1:15355878
|
CA | C | 69 | a0001c0001t0002g0049a0001c0001t0002g0057a0001c0002t0001g0019others(66): Show | 69 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.2563-2224delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15355878 | |||||
| chr1:15355906
|
TA | T | 69 | a0001c0001t0002g0049a0001c0001t0002g0057a0001c0002t0001g0019others(66): Show | 69 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.2563-2195delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15355906 | |||||
| chr1:15355907
|
A | T | 3 | a0025c0042t0003g0010a0025c0042t0003g0011a0062c0062t0011g0285 | 3 | HG01069.hp1 HG01071.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2563-2203A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15355907 | ||||||
| chr1:15355936
|
G | GA | 52 | a0001c0001t0013g0104a0001c0002t0018g0156a0001c0002t0049g0101others(49): Show | 52 | HG00621.hp2 HG00735.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.2563-2159dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15355936 | |||||
| chr1:15355936
|
G | GAAA | 10 | a0007c0012t0026g0245a0007c0012t0026g0246a0018c0020t0022g0239others(7): Show | 10 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.2563-2161_2563-215 others(7): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15355936 | |||||
| chr1:15355936
|
GA | G | 8 | a0001c0010t0001g0097a0001c0010t0001g0098a0006c0014t0005g0255others(5): Show | 8 | HG00642.hp2 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.2563-2159delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15355936 | |||||
| chr1:15355986
|
T | G | 129 | a0001c0001t0002g0049a0001c0001t0002g0057a0001c0001t0013g0104others(126): Show | 129 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.2563-2124T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15355986 | ||||||
| chr1:15356019
|
A | G | 89 | a0001c0001t0002g0049a0001c0001t0002g0057a0001c0002t0001g0019others(86): Show | 89 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.2563-2091A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15356019 | ||||||
| chr1:15356081
|
A | G | 2 | a0037c0128t0007g0233a0038c0129t0007g0235 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2563-2029A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15356081 | ||||||
| chr1:15356176
|
A | G | 1 | a0007c0012t0016g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2563-1934A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15356176 | ||||||
| chr1:15356270
|
C | T | 1 | a0002c0007t0005g0212 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2563-1840C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15356270 | ||||||
| chr1:15356374
|
AG | A | 3 | a0016c0107t0003g0145a0023c0127t0019g0184a0041c0076t0038g0289 | 3 | HG02145.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2563-1735delG | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15356374 | ||||||
| chr1:15356407
|
A | G | 10 | a0001c0032t0014g0152a0003c0086t0009g0142a0004c0038t0007g0143others(7): Show | 10 | HG01070.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2563-1703A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15356407 | ||||||
| chr1:15356450
|
G | A | 10 | a0001c0032t0014g0152a0003c0086t0009g0142a0004c0038t0007g0143others(7): Show | 10 | HG01070.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2563-1660G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15356450 | ||||||
| chr1:15356501
|
C | T | 1 | a0002c0007t0005g0210 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2563-1609C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15356501 | ||||||
| chr1:15356582
|
A | G | 1 | a0007c0033t0014g0068 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2563-1528A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15356582 | ||||||
| chr1:15356637
|
C | G | 1 | a0004c0038t0007g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2563-1473C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15356637 | ||||||
| chr1:15356687
|
C | T | 2 | a0037c0128t0007g0233a0038c0129t0007g0235 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2563-1423C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15356687 | ||||||
| chr1:15356792
|
A | C | 2 | a0037c0128t0007g0233a0038c0129t0007g0235 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2563-1318A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15356792 | ||||||
| chr1:15356871
|
CA | C | 101 | a0001c0001t0002g0049a0001c0001t0002g0057a0001c0001t0010g0281others(98): Show | 101 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.2563-1223delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15356871 | |||||
| chr1:15356871
|
CAA | C | 10 | a0001c0015t0001g0109a0001c0015t0001g0110a0001c0015t0001g0111others(7): Show | 10 | HG01070.hp1 HG01123.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.2563-1224_2563-122 others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15356871 | |||||
| chr1:15356913
|
T | A | 16 | a0001c0032t0014g0152a0003c0086t0009g0142a0004c0038t0007g0143others(13): Show | 16 | HG01070.hp1 HG01884.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2563-1197T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15356913 | ||||||
| chr1:15357033
|
G | A | 1 | a0020c0111t0030g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2563-1077G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15357033 | ||||||
| chr1:15357150
|
G | A | 2 | a0004c0087t0046g0121a0007c0033t0014g0068 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2563-960G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15357150 | ||||||
| chr1:15357364
|
G | A | 1 | a0020c0111t0030g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2563-746G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15357364 | ||||||
| chr1:15357391
|
G | T | 3 | a0001c0032t0023g0282a0003c0085t0055g0139a0007c0033t0007g0138 | 3 | HG02717.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2563-719G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15357391 | ||||||
| chr1:15357407
|
G | A | 1 | a0002c0018t0018g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2563-703G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15357407 | ||||||
| chr1:15357491
|
C | T | 10 | a0007c0012t0026g0245a0007c0012t0026g0246a0018c0020t0022g0239others(7): Show | 10 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.2563-619C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15357491 | ||||||
| chr1:15357555
|
G | A | 10 | a0004c0087t0046g0121a0006c0014t0005g0255a0007c0012t0016g0187others(7): Show | 10 | HG00642.hp2 HG02145.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2563-555G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15357555 | ||||||
| chr1:15357588
|
G | A | 4 | a0002c0018t0007g0140a0002c0018t0021g0247a0014c0112t0007g0202others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2563-522G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15357588 | ||||||
| chr1:15357620
|
C | T | 2 | a0037c0128t0007g0233a0038c0129t0007g0235 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2563-490C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | chr1 | 15357620 | ||||||
| chr1:15357625
|
C | CA | 19 | a0001c0001t0008g0129a0001c0002t0001g0063a0001c0002t0001g0079others(16): Show | 19 | HG00423.hp1 HG01070.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.2563-463dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15357625 | |||||
| chr1:15357625
|
CA | C | 85 | a0001c0001t0002g0049a0001c0001t0002g0057a0001c0001t0057g0250others(82): Show | 85 | HG00423.hp2 HG00609.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.2563-463delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15357625 | |||||
| chr1:15357625
|
CAA | C | 7 | a0001c0002t0044g0169a0001c0010t0001g0182a0002c0080t0019g0181others(4): Show | 7 | HG02717.hp2 HG02896.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2563-464_2563-463d others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15357625 | |||||
| chr1:15357625
|
CAAAAAAA | C | 13 | a0001c0001t0013g0104a0001c0002t0018g0156a0001c0002t0049g0101others(10): Show | 13 | HG00735.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2563-469_2563-463d others(9): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15357625 | |||||
| chr1:15357625
|
CAAAAAAA others(4): Show |
C | 1 | a0065c0064t0041g0006 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2563-473_2563-463d others(13): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr1 | 15357625 | |||||
| chr1:15358499
|
A | G | 218 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0054others(215): Show | 218 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(215): Show |
intron_variant | MODIFIER | c.2736+216A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15358499 | ||||||
| chr1:15358504
|
C | T | 1 | a0001c0013t0011g0266 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2736+221C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15358504 | ||||||
| chr1:15358866
|
G | A | 163 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0054others(160): Show | 163 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.2736+583G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15358866 | ||||||
| chr1:15358942
|
CGGGAGCT others(2): Show |
C | 9 | a0001c0032t0023g0282a0002c0018t0018g0153a0002c0019t0027g0244others(6): Show | 9 | HG01069.hp1 HG01071.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2736+665_2736+673d others(11): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | INFO_REALIGN_3_PRIME | chr1 | 15358942 | |||||
| chr1:15359038
|
G | A | 1 | a0038c0129t0007g0235 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2736+755G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359038 | ||||||
| chr1:15359060
|
ACACTT | A | 6 | a0001c0090t0048g0158a0002c0003t0014g0151a0002c0080t0019g0181others(3): Show | 6 | HG02055.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2736+780_2736+784d others(7): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | INFO_REALIGN_3_PRIME | chr1 | 15359060 | |||||
| chr1:15359077
|
G | A | 12 | a0001c0001t0013g0104a0001c0002t0018g0156a0001c0002t0049g0101others(9): Show | 12 | HG00735.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2736+794G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359077 | ||||||
| chr1:15359159
|
G | A | 1 | a0002c0019t0027g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2736+876G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359159 | ||||||
| chr1:15359197
|
C | T | 1 | a0002c0134t0003g0209 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2736+914C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359197 | ||||||
| chr1:15359262
|
A | G | 1 | a0032c0120t0034g0259 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2736+979A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359262 | ||||||
| chr1:15359301
|
T | C | 220 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0054others(217): Show | 220 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(217): Show |
intron_variant | MODIFIER | c.2736+1018T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359301 | ||||||
| chr1:15359361
|
G | C | 1 | a0001c0002t0044g0169 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2736+1078G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359361 | ||||||
| chr1:15359472
|
A | C | 14 | a0007c0012t0026g0245a0007c0012t0026g0246a0017c0017t0007g0008others(11): Show | 14 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2737-1006A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359472 | ||||||
| chr1:15359479
|
C | T | 1 | a0001c0102t0012g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2737-999C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359479 | ||||||
| chr1:15359510
|
A | G | 224 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0054others(221): Show | 224 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(221): Show |
intron_variant | MODIFIER | c.2737-968A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359510 | ||||||
| chr1:15359675
|
C | T | 1 | a0004c0004t0004g0086 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2737-803C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359675 | ||||||
| chr1:15359726
|
G | A | 1 | a0001c0001t0057g0250 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2737-752G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359726 | ||||||
| chr1:15359746
|
C | T | 2 | a0003c0006t0008g0134a0003c0056t0001g0107 | 2 | HG02602.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2737-732C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359746 | ||||||
| chr1:15359759
|
G | A | 1 | a0001c0001t0010g0281 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2737-719G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359759 | ||||||
| chr1:15359777
|
T | C | 3 | a0001c0013t0001g0051a0009c0071t0017g0291a0010c0029t0017g0276 | 3 | HG01081.hp1 HG01081.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.2737-701T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359777 | ||||||
| chr1:15359778
|
A | G | 3 | a0001c0013t0001g0051a0009c0071t0017g0291a0010c0029t0017g0276 | 3 | HG01081.hp1 HG01081.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.2737-700A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359778 | ||||||
| chr1:15359810
|
CGT | C | 21 | a0001c0001t0008g0160a0001c0001t0013g0028a0001c0001t0015g0267others(18): Show | 21 | HG00642.hp2 HG01106.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.2737-666_2737-665d others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | INFO_REALIGN_3_PRIME | chr1 | 15359810 | |||||
| chr1:15359818
|
C | T | 8 | a0001c0002t0001g0023a0002c0019t0027g0244a0011c0025t0003g0208others(5): Show | 8 | HG00544.hp1 HG00558.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2737-660C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359818 | ||||||
| chr1:15359823
|
G | GCCTGTAG others(156): Show |
1 | a0001c0032t0014g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2737-646_2737-484d others(165): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | INFO_REALIGN_3_PRIME | chr1 | 15359823 | |||||
| chr1:15359825
|
C | T | 2 | a0003c0098t0029g0237a0007c0101t0014g0119 | 2 | HG00738.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2737-653C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359825 | ||||||
| chr1:15359827
|
G | A | 13 | a0001c0010t0001g0182a0002c0019t0027g0244a0003c0098t0029g0237others(10): Show | 13 | HG00738.hp2 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.2737-651G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359827 | ||||||
| chr1:15359832
|
CCCAGCTA others(156): Show |
C | 1 | a0013c0021t0008g0136 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2737-614_2737-452d others(2): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | INFO_REALIGN_3_PRIME | chr1 | 15359832 | |||||
| chr1:15359907
|
G | A | 2 | a0006c0014t0005g0255a0021c0113t0016g0194 | 2 | HG00642.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2737-571G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359907 | ||||||
| chr1:15359915
|
A | C | 2 | a0001c0001t0002g0040a0001c0008t0008g0204 | 2 | HG02056.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.2737-563A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359915 | ||||||
| chr1:15359936
|
A | C | 161 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(158): Show | 161 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.2737-542A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359936 | ||||||
| chr1:15359981
|
C | T | 1 | a0001c0108t0001g0165 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2737-497C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15359981 | ||||||
| chr1:15360068
|
G | A | 65 | a0001c0001t0008g0160a0001c0001t0013g0028a0001c0001t0013g0104others(62): Show | 65 | HG00735.hp2 HG01070.hp1 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.2737-410G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15360068 | ||||||
| chr1:15360118
|
A | AAAC | 5 | a0002c0080t0019g0181a0004c0038t0014g0155a0005c0070t0035g0287others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2737-345_2737-343d others(5): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | INFO_REALIGN_3_PRIME | chr1 | 15360118 | |||||
| chr1:15360154
|
G | A | 4 | a0001c0001t0057g0250a0009c0011t0019g0144a0039c0126t0019g0185others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2737-324G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15360154 | ||||||
| chr1:15360289
|
C | T | 1 | a0004c0004t0004g0027 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2737-189C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15360289 | ||||||
| chr1:15360338
|
C | T | 41 | a0001c0001t0002g0093a0001c0001t0002g0099a0001c0001t0012g0161others(38): Show | 41 | HG00609.hp1 HG01069.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.2737-140C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 21/33 | chr1 | 15360338 | ||||||
| chr1:15360761
|
G | A | 1 | a0007c0059t0014g0167 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2962+58G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 22/33 | chr1 | 15360761 | ||||||
| chr1:15360832
|
C | T | 1 | a0032c0120t0034g0259 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2962+129C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 22/33 | chr1 | 15360832 | ||||||
| chr1:15360983
|
C | T | 1 | a0002c0007t0003g0190 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2962+280C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 22/33 | chr1 | 15360983 | ||||||
| chr1:15361058
|
C | T | 1 | a0002c0007t0003g0190 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2962+355C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 22/33 | chr1 | 15361058 | ||||||
| chr1:15361188
|
C | G | 2 | a0002c0019t0027g0244a0012c0079t0027g0248 | 2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2962+485C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 22/33 | chr1 | 15361188 | ||||||
| chr1:15361318
|
A | G | 118 | a0001c0001t0002g0057a0001c0001t0013g0104a0001c0002t0018g0156others(115): Show | 118 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.2962+615A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 22/33 | chr1 | 15361318 | ||||||
| chr1:15361549
|
A | G | 109 | a0001c0001t0002g0057a0001c0001t0013g0104a0001c0002t0018g0156others(106): Show | 109 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.2962+846A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 22/33 | chr1 | 15361549 | ||||||
| chr1:15361710
|
C | CT | 5 | a0001c0090t0048g0158a0002c0003t0014g0151a0003c0085t0055g0139others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2963-931dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 22/33 | INFO_REALIGN_3_PRIME | chr1 | 15361710 | |||||
| chr1:15361878
|
G | A | 17 | a0002c0018t0007g0140a0002c0018t0021g0247a0007c0012t0016g0187others(14): Show | 17 | HG00735.hp2 HG00738.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.2963-764G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 22/33 | chr1 | 15361878 | ||||||
| chr1:15361936
|
G | A | 1 | a0014c0110t0008g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2963-706G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 22/33 | chr1 | 15361936 | ||||||
| chr1:15362010
|
A | C | 1 | a0059c0104t0045g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2963-632A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 22/33 | chr1 | 15362010 | ||||||
| chr1:15362087
|
T | G | 11 | a0002c0035t0006g0026a0002c0053t0020g0096a0004c0058t0006g0183others(8): Show | 11 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.2963-555T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 22/33 | chr1 | 15362087 | ||||||
| chr1:15362123
|
G | A | 1 | a0002c0003t0006g0157 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2963-519G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 22/33 | chr1 | 15362123 | ||||||
| chr1:15362233
|
C | G | 1 | a0005c0005t0010g0279 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2963-409C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 22/33 | chr1 | 15362233 | ||||||
| chr1:15362561
|
T | A | 1 | a0003c0098t0029g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2963-81T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 22/33 | chr1 | 15362561 | ||||||
| chr1:15362576
|
G | A | 1 | a0001c0002t0009g0162 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2963-66G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 22/33 | chr1 | 15362576 | ||||||
| chr1:15363148
|
C | T | 3 | a0007c0033t0007g0138a0007c0033t0014g0068a0046c0078t0007g0232 | 3 | HG02280.hp2 HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3047+422C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | chr1 | 15363148 | ||||||
| chr1:15363340
|
C | T | 1 | a0003c0037t0001g0094 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3047+614C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | chr1 | 15363340 | ||||||
| chr1:15363432
|
A | T | 1 | a0032c0120t0034g0259 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3047+706A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | chr1 | 15363432 | ||||||
| chr1:15363716
|
C | T | 1 | a0002c0019t0027g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3047+990C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | chr1 | 15363716 | ||||||
| chr1:15363795
|
C | T | 3 | a0025c0042t0003g0010a0025c0042t0003g0011a0062c0062t0011g0285 | 3 | HG01069.hp1 HG01071.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3047+1069C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | chr1 | 15363795 | ||||||
| chr1:15363858
|
G | A | 1 | a0009c0011t0019g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3047+1132G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | chr1 | 15363858 | ||||||
| chr1:15364027
|
G | A | 3 | a0029c0114t0056g0199a0047c0089t0050g0105a0060c0065t0043g0005 | 3 | HG01167.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3047+1301G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | chr1 | 15364027 | ||||||
| chr1:15364046
|
A | C | 1 | a0002c0003t0005g0172 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3047+1320A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | chr1 | 15364046 | ||||||
| chr1:15364193
|
A | G | 2 | a0001c0010t0001g0097a0001c0010t0001g0098 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3047+1467A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | chr1 | 15364193 | ||||||
| chr1:15364276
|
A | G | 1 | a0014c0110t0008g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3047+1550A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | chr1 | 15364276 | ||||||
| chr1:15364458
|
A | G | 17 | a0002c0018t0007g0140a0002c0018t0021g0247a0007c0012t0016g0187others(14): Show | 17 | HG00735.hp2 HG00738.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.3048-1369A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | chr1 | 15364458 | ||||||
| chr1:15364525
|
A | G | 1 | a0007c0101t0014g0119 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3048-1302A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | chr1 | 15364525 | ||||||
| chr1:15364588
|
C | T | 1 | a0020c0111t0030g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3048-1239C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | chr1 | 15364588 | ||||||
| chr1:15364644
|
A | G | 3 | a0025c0042t0003g0010a0025c0042t0003g0011a0062c0062t0011g0285 | 3 | HG01069.hp1 HG01071.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3048-1183A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | chr1 | 15364644 | ||||||
| chr1:15365044
|
A | C | 104 | a0001c0001t0002g0049a0001c0001t0002g0057a0001c0001t0013g0104others(101): Show | 104 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(101): Show |
intron_variant | MODIFIER | c.3048-783A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | chr1 | 15365044 | ||||||
| chr1:15365345
|
T | C | 11 | a0002c0035t0006g0026a0002c0053t0020g0096a0004c0058t0006g0183others(8): Show | 11 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.3048-482T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | chr1 | 15365345 | ||||||
| chr1:15365481
|
A | AT | 9 | a0001c0008t0002g0095a0001c0032t0014g0152a0001c0032t0023g0282others(6): Show | 9 | HG02622.hp1 HG02717.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.3048-326dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | INFO_REALIGN_3_PRIME | chr1 | 15365481 | |||||
| chr1:15365481
|
A | ATTTTTTT others(3): Show |
5 | a0001c0001t0013g0104a0001c0002t0018g0156a0005c0005t0015g0286others(2): Show | 5 | HG01069.hp1 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3048-335_3048-326d others(12): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | INFO_REALIGN_3_PRIME | chr1 | 15365481 | |||||
| chr1:15365481
|
A | ATTTTTTT others(4): Show |
55 | a0001c0001t0002g0057a0001c0002t0049g0101a0001c0010t0001g0182others(52): Show | 55 | HG00423.hp2 HG00738.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.3048-336_3048-326d others(13): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | INFO_REALIGN_3_PRIME | chr1 | 15365481 | |||||
| chr1:15365481
|
A | ATTTTTTT others(5): Show |
16 | a0001c0102t0012g0146a0002c0003t0004g0044a0002c0053t0020g0096others(13): Show | 16 | HG00621.hp2 HG01106.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.3048-337_3048-326d others(14): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | INFO_REALIGN_3_PRIME | chr1 | 15365481 | |||||
| chr1:15365481
|
A | ATTTTTTT others(6): Show |
8 | a0002c0003t0004g0017a0002c0003t0005g0135a0002c0007t0005g0210others(5): Show | 8 | HG02015.hp2 HG02056.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.3048-338_3048-326d others(15): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | INFO_REALIGN_3_PRIME | chr1 | 15365481 | |||||
| chr1:15365481
|
A | ATTTTTTT others(7): Show |
1 | a0033c0131t0005g0219 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3048-339_3048-326d others(16): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | INFO_REALIGN_3_PRIME | chr1 | 15365481 | |||||
| chr1:15365481
|
A | ATTTTTTT others(9): Show |
3 | a0009c0011t0017g0263a0029c0114t0056g0199a0047c0089t0050g0105 | 3 | HG01167.hp1 HG02922.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3048-341_3048-326d others(18): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | INFO_REALIGN_3_PRIME | chr1 | 15365481 | |||||
| chr1:15365481
|
A | ATTTTTTT others(10): Show |
4 | a0001c0090t0048g0158a0002c0003t0014g0151a0040c0077t0037g0262others(1): Show | 4 | HG02055.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.3048-342_3048-326d others(19): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | INFO_REALIGN_3_PRIME | chr1 | 15365481 | |||||
| chr1:15365481
|
A | ATTTTTTT others(11): Show |
2 | a0003c0085t0055g0139a0066c0061t0042g0007 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3048-343_3048-326d others(20): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | INFO_REALIGN_3_PRIME | chr1 | 15365481 | |||||
| chr1:15365481
|
AT | A | 15 | a0001c0001t0008g0127a0002c0018t0007g0140a0002c0018t0021g0247others(12): Show | 15 | HG00735.hp2 HG00738.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.3048-326delT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | INFO_REALIGN_3_PRIME | chr1 | 15365481 | |||||
| chr1:15365489
|
T | TTTTTTTT others(4): Show |
1 | a0002c0003t0006g0157 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3048-328_3048-327i others(13): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | INFO_REALIGN_3_PRIME | chr1 | 15365489 | |||||
| chr1:15365503
|
T | G | 3 | a0029c0114t0056g0199a0047c0089t0050g0105a0060c0065t0043g0005 | 3 | HG01167.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3048-324T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | chr1 | 15365503 | ||||||
| chr1:15365545
|
A | G | 2 | a0001c0001t0002g0057a0003c0006t0002g0090 | 2 | NA19000.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.3048-282A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | chr1 | 15365545 | ||||||
| chr1:15365714
|
T | G | 11 | a0002c0035t0006g0026a0002c0053t0020g0096a0004c0058t0006g0183others(8): Show | 11 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.3048-113T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 23/33 | chr1 | 15365714 | ||||||
| chr1:15366014
|
G | T | 11 | a0002c0035t0006g0026a0002c0053t0020g0096a0004c0058t0006g0183others(8): Show | 11 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.3154+81G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15366014 | ||||||
| chr1:15366203
|
T | C | 1 | a0001c0002t0001g0063 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3154+270T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15366203 | ||||||
| chr1:15366241
|
C | T | 3 | a0029c0114t0056g0199a0047c0089t0050g0105a0060c0065t0043g0005 | 3 | HG01167.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3154+308C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15366241 | ||||||
| chr1:15366260
|
G | A | 3 | a0007c0033t0007g0138a0007c0033t0014g0068a0046c0078t0007g0232 | 3 | HG02280.hp2 HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3154+327G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15366260 | ||||||
| chr1:15366284
|
C | CA | 15 | a0001c0002t0001g0078a0001c0002t0001g0102a0001c0008t0008g0204others(12): Show | 15 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.3154+376dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | INFO_REALIGN_3_PRIME | chr1 | 15366284 | |||||
| chr1:15366284
|
C | CAA | 10 | a0002c0035t0006g0026a0002c0053t0020g0096a0004c0058t0006g0183others(7): Show | 10 | HG00438.hp1 HG00738.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.3154+375_3154+376d others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | INFO_REALIGN_3_PRIME | chr1 | 15366284 | |||||
| chr1:15366284
|
C | CAAA | 16 | a0002c0003t0004g0017a0002c0003t0005g0135a0002c0007t0005g0210others(13): Show | 16 | HG01069.hp2 HG01109.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.3154+374_3154+376d others(5): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | INFO_REALIGN_3_PRIME | chr1 | 15366284 | |||||
| chr1:15366284
|
C | CAAAA | 48 | a0001c0001t0002g0049a0001c0010t0001g0182a0001c0013t0011g0266others(45): Show | 48 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.3154+373_3154+376d others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | INFO_REALIGN_3_PRIME | chr1 | 15366284 | |||||
| chr1:15366284
|
C | CAAAAA | 13 | a0001c0001t0002g0057a0001c0001t0013g0104a0001c0002t0018g0156others(10): Show | 13 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.3154+372_3154+376d others(7): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | INFO_REALIGN_3_PRIME | chr1 | 15366284 | |||||
| chr1:15366417
|
G | C | 123 | a0001c0001t0002g0057a0001c0001t0013g0104a0001c0002t0018g0156others(120): Show | 123 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.3154+484G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15366417 | ||||||
| chr1:15366447
|
C | T | 1 | a0004c0087t0046g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3154+514C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15366447 | ||||||
| chr1:15366568
|
G | A | 1 | a0022c0046t0009g0222 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3154+635G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15366568 | ||||||
| chr1:15366719
|
C | T | 2 | a0002c0035t0006g0026a0012c0097t0003g0141 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3155-744C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15366719 | ||||||
| chr1:15366740
|
A | C | 1 | a0020c0111t0030g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3155-723A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15366740 | ||||||
| chr1:15366781
|
G | A | 3 | a0015c0023t0008g0123a0015c0023t0008g0130a0015c0023t0008g0131 | 3 | NA18960.hp2 NA18977.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.3155-682G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15366781 | ||||||
| chr1:15366928
|
T | C | 2 | a0002c0035t0006g0031a0005c0072t0010g0270 | 2 | HG00735.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.3155-535T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15366928 | ||||||
| chr1:15367060
|
A | T | 92 | a0001c0001t0002g0057a0001c0001t0013g0104a0001c0002t0018g0156others(89): Show | 92 | HG00423.hp2 HG00621.hp2 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.3155-403A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15367060 | ||||||
| chr1:15367076
|
G | A | 3 | a0029c0114t0056g0199a0047c0089t0050g0105a0060c0065t0043g0005 | 3 | HG01167.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3155-387G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15367076 | ||||||
| chr1:15367178
|
A | T | 145 | a0001c0001t0002g0057a0001c0001t0013g0104a0001c0002t0018g0156others(142): Show | 145 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.3155-285A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15367178 | ||||||
| chr1:15367221
|
G | A | 1 | a0046c0078t0007g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3155-242G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15367221 | ||||||
| chr1:15367228
|
C | A | 1 | a0002c0018t0007g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3155-235C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15367228 | ||||||
| chr1:15367295
|
A | G | 1 | a0003c0006t0002g0122 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3155-168A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15367295 | ||||||
| chr1:15367365
|
G | A | 3 | a0002c0003t0006g0157a0036c0121t0007g0201a0051c0100t0001g0091 | 3 | HG01069.hp2 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3155-98G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15367365 | ||||||
| chr1:15367373
|
G | A | 1 | a0001c0013t0001g0053 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3155-90G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15367373 | ||||||
| chr1:15367382
|
C | T | 3 | a0029c0114t0056g0199a0047c0089t0050g0105a0060c0065t0043g0005 | 3 | HG01167.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3155-81C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15367382 | ||||||
| chr1:15367456
|
C | G | 1 | a0014c0110t0008g0254 | 1 | HG02572.hp1 | splice_region_variant&intron_variant | LOW | c.3155-7C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 24/33 | chr1 | 15367456 | ||||||
| chr1:15367641
|
G | A | 36 | a0002c0003t0003g0133a0002c0003t0006g0064a0002c0003t0006g0069others(33): Show | 36 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.3314+19G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15367641 | ||||||
| chr1:15367649
|
G | T | 1 | a0002c0003t0004g0044 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3314+27G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15367649 | ||||||
| chr1:15367666
|
G | A | 8 | a0002c0080t0019g0181a0017c0017t0007g0008a0017c0017t0007g0147others(5): Show | 8 | HG02257.hp1 HG02486.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.3314+44G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15367666 | ||||||
| chr1:15367674
|
C | T | 1 | a0006c0014t0005g0255 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3314+52C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15367674 | ||||||
| chr1:15368132
|
T | A | 1 | a0002c0003t0004g0044 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3314+510T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368132 | ||||||
| chr1:15368146
|
G | A | 5 | a0001c0001t0002g0093a0001c0001t0002g0099a0001c0001t0013g0048others(2): Show | 5 | NA18943.hp2 NA18955.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.3314+524G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368146 | ||||||
| chr1:15368226
|
G | A | 1 | a0012c0051t0011g0284 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3314+604G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368226 | ||||||
| chr1:15368260
|
C | T | 11 | a0002c0018t0007g0140a0002c0018t0021g0247a0007c0012t0016g0187others(8): Show | 11 | HG02615.hp1 HG02630.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.3314+638C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368260 | ||||||
| chr1:15368270
|
G | A | 10 | a0002c0035t0006g0026a0002c0053t0020g0096a0004c0058t0006g0183others(7): Show | 10 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.3314+648G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368270 | ||||||
| chr1:15368314
|
G | T | 2 | a0036c0121t0007g0201a0051c0100t0001g0091 | 2 | HG01069.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3314+692G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368314 | ||||||
| chr1:15368460
|
C | T | 2 | a0004c0004t0007g0001a0004c0004t0007g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.3314+838C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368460 | ||||||
| chr1:15368465
|
T | A | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3314+843T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368465 | ||||||
| chr1:15368466
|
G | C | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3314+844G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368466 | ||||||
| chr1:15368468
|
G | A | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3314+846G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368468 | ||||||
| chr1:15368469
|
T | A | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3314+847T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368469 | ||||||
| chr1:15368474
|
T | C | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3314+852T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368474 | ||||||
| chr1:15368475
|
T | A | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3314+853T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368475 | ||||||
| chr1:15368476
|
T | A | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3314+854T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368476 | ||||||
| chr1:15368480
|
C | A | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3314+858C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368480 | ||||||
| chr1:15368481
|
C | T | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3314+859C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368481 | ||||||
| chr1:15368486
|
G | T | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3314+864G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368486 | ||||||
| chr1:15368487
|
C | T | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3314+865C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368487 | ||||||
| chr1:15368488
|
T | G | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3314+866T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368488 | ||||||
| chr1:15368492
|
C | G | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3314+870C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368492 | ||||||
| chr1:15368494
|
A | T | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3314+872A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368494 | ||||||
| chr1:15368495
|
T | A | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3314+873T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368495 | ||||||
| chr1:15368496
|
A | T | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3314+874A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368496 | ||||||
| chr1:15368502
|
G | A | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-868G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368502 | ||||||
| chr1:15368503
|
A | G | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-867A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368503 | ||||||
| chr1:15368504
|
A | C | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-866A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368504 | ||||||
| chr1:15368508
|
G | C | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-862G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368508 | ||||||
| chr1:15368512
|
T | A | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-858T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368512 | ||||||
| chr1:15368517
|
T | A | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-853T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368517 | ||||||
| chr1:15368518
|
C | T | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-852C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368518 | ||||||
| chr1:15368519
|
A | T | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-851A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368519 | ||||||
| chr1:15368520
|
C | CA | 6 | a0007c0059t0014g0167a0007c0101t0014g0119a0009c0028t0011g0290others(3): Show | 6 | HG00735.hp2 HG00738.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.3315-842dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | INFO_REALIGN_3_PRIME | chr1 | 15368520 | |||||
| chr1:15368521
|
A | C | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-849A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368521 | ||||||
| chr1:15368539
|
G | T | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-831G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368539 | ||||||
| chr1:15368544
|
T | A | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-826T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368544 | ||||||
| chr1:15368545
|
G | A | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-825G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368545 | ||||||
| chr1:15368548
|
G | A | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-822G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368548 | ||||||
| chr1:15368552
|
T | A | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-818T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368552 | ||||||
| chr1:15368562
|
T | A | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-808T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368562 | ||||||
| chr1:15368563
|
G | C | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-807G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368563 | ||||||
| chr1:15368564
|
G | T | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-806G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368564 | ||||||
| chr1:15368586
|
C | T | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-784C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368586 | ||||||
| chr1:15368588
|
A | G | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-782A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368588 | ||||||
| chr1:15368589
|
A | G | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-781A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368589 | ||||||
| chr1:15368595
|
T | A | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-775T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368595 | ||||||
| chr1:15368607
|
C | G | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-763C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368607 | ||||||
| chr1:15368608
|
T | C | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-762T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368608 | ||||||
| chr1:15368614
|
A | T | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-756A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368614 | ||||||
| chr1:15368615
|
G | C | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-755G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368615 | ||||||
| chr1:15368616
|
C | T | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-754C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368616 | ||||||
| chr1:15368618
|
G | C | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-752G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368618 | ||||||
| chr1:15368631
|
G | T | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-739G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368631 | ||||||
| chr1:15368633
|
T | C | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-737T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368633 | ||||||
| chr1:15368634
|
G | T | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-736G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368634 | ||||||
| chr1:15368636
|
C | G | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-734C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368636 | ||||||
| chr1:15368642
|
T | G | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-728T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368642 | ||||||
| chr1:15368644
|
A | G | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-726A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368644 | ||||||
| chr1:15368646
|
A | G | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-724A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368646 | ||||||
| chr1:15368648
|
C | G | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-722C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368648 | ||||||
| chr1:15368654
|
C | A | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-716C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368654 | ||||||
| chr1:15368655
|
C | A | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-715C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368655 | ||||||
| chr1:15368657
|
A | AAACAGGC others(7): Show |
1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-713_3315-712i others(16): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368657 | ||||||
| chr1:15368659
|
A | G | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-711A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368659 | ||||||
| chr1:15368662
|
A | G | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-708A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368662 | ||||||
| chr1:15368666
|
C | G | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-704C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368666 | ||||||
| chr1:15368668
|
A | G | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-702A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368668 | ||||||
| chr1:15368705
|
T | C | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-665T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368705 | ||||||
| chr1:15368711
|
A | G | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-659A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368711 | ||||||
| chr1:15368717
|
A | G | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-653A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368717 | ||||||
| chr1:15368723
|
C | T | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-647C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368723 | ||||||
| chr1:15368737
|
T | C | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-633T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368737 | ||||||
| chr1:15368760
|
A | G | 3 | a0002c0007t0003g0186a0004c0004t0004g0116a0067c0049t0005g0236 | 3 | NA18955.hp1 NA18956.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.3315-610A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368760 | ||||||
| chr1:15368763
|
G | T | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-607G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368763 | ||||||
| chr1:15368766
|
A | T | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-604A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368766 | ||||||
| chr1:15368768
|
C | T | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-602C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368768 | ||||||
| chr1:15368770
|
T | C | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-600T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368770 | ||||||
| chr1:15368771
|
G | A | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-599G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368771 | ||||||
| chr1:15368801
|
T | G | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-569T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368801 | ||||||
| chr1:15368802
|
G | C | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-568G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368802 | ||||||
| chr1:15368809
|
T | C | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-561T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368809 | ||||||
| chr1:15368810
|
G | T | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-560G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368810 | ||||||
| chr1:15368826
|
T | G | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-544T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368826 | ||||||
| chr1:15368831
|
G | C | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-539G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368831 | ||||||
| chr1:15368832
|
G | A | 1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3315-538G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15368832 | ||||||
| chr1:15369090
|
A | C | 1 | a0002c0003t0006g0157 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3315-280A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15369090 | ||||||
| chr1:15369097
|
T | C | 1 | a0007c0082t0016g0180 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3315-273T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15369097 | ||||||
| chr1:15369115
|
A | C | 62 | a0001c0001t0002g0057a0001c0001t0013g0104a0001c0002t0018g0156others(59): Show | 62 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.3315-255A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15369115 | ||||||
| chr1:15369346
|
C | T | 8 | a0002c0003t0004g0017a0002c0003t0005g0135a0002c0007t0005g0210others(5): Show | 8 | HG02015.hp2 HG02056.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.3315-24C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 25/33 | chr1 | 15369346 | ||||||
| chr1:15369570
|
C | G | 9 | a0004c0004t0007g0001a0004c0004t0007g0002a0004c0038t0007g0143others(6): Show | 9 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.3447+68C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15369570 | ||||||
| chr1:15369640
|
G | A | 4 | a0001c0039t0001g0037a0029c0114t0056g0199a0047c0089t0050g0105others(1): Show | 4 | HG01167.hp1 HG02922.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.3447+138G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15369640 | ||||||
| chr1:15369777
|
G | T | 1 | a0011c0025t0003g0211 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3447+275G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15369777 | ||||||
| chr1:15370009
|
C | A | 2 | a0036c0121t0007g0201a0051c0100t0001g0091 | 2 | HG01069.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3447+507C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15370009 | ||||||
| chr1:15370014
|
A | G | 16 | a0002c0018t0007g0140a0002c0018t0021g0247a0007c0012t0016g0187others(13): Show | 16 | HG00735.hp2 HG00738.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.3447+512A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15370014 | ||||||
| chr1:15370305
|
T | A | 1 | a0004c0087t0046g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3447+803T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15370305 | ||||||
| chr1:15370439
|
T | C | 2 | a0002c0003t0006g0069a0002c0003t0006g0089 | 2 | NA18984.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.3447+937T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15370439 | ||||||
| chr1:15370462
|
C | T | 1 | a0007c0101t0014g0119 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3447+960C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15370462 | ||||||
| chr1:15370481
|
G | A | 8 | a0002c0003t0004g0017a0002c0003t0005g0135a0002c0007t0005g0210others(5): Show | 8 | HG02015.hp2 HG02056.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.3447+979G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15370481 | ||||||
| chr1:15370563
|
G | T | 3 | a0009c0011t0019g0144a0023c0127t0019g0184a0041c0076t0038g0289 | 3 | HG02486.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3447+1061G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15370563 | ||||||
| chr1:15370687
|
A | G | 128 | a0001c0001t0002g0057a0001c0001t0013g0104a0001c0002t0018g0156others(125): Show | 128 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.3447+1185A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15370687 | ||||||
| chr1:15370722
|
G | A | 1 | a0006c0014t0003g0224 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3447+1220G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15370722 | ||||||
| chr1:15370870
|
G | T | 1 | a0007c0012t0016g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3447+1368G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15370870 | ||||||
| chr1:15370919
|
C | G | 1 | a0001c0001t0012g0128 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3447+1417C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15370919 | ||||||
| chr1:15371092
|
C | T | 2 | a0019c0022t0004g0022a0019c0022t0004g0071 | 2 | NA18992.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.3447+1590C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15371092 | ||||||
| chr1:15371196
|
C | T | 1 | a0009c0011t0019g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3447+1694C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15371196 | ||||||
| chr1:15371211
|
A | G | 2 | a0007c0059t0014g0167a0007c0101t0014g0119 | 2 | HG00735.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.3447+1709A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15371211 | ||||||
| chr1:15371430
|
G | C | 63 | a0001c0001t0002g0057a0001c0001t0013g0104a0001c0002t0018g0156others(60): Show | 63 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.3447+1928G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15371430 | ||||||
| chr1:15371430
|
G | T | 1 | a0003c0086t0009g0142 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3447+1928G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15371430 | ||||||
| chr1:15371431
|
G | A | 1 | a0001c0010t0001g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3447+1929G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15371431 | ||||||
| chr1:15371587
|
C | T | 12 | a0001c0002t0001g0058a0001c0002t0001g0076a0001c0002t0044g0169others(9): Show | 12 | HG00609.hp1 HG00621.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.3447+2085C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15371587 | ||||||
| chr1:15371626
|
T | A | 2 | a0036c0121t0007g0201a0051c0100t0001g0091 | 2 | HG01069.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3447+2124T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15371626 | ||||||
| chr1:15371672
|
G | A | 4 | a0002c0018t0007g0140a0002c0018t0021g0247a0014c0112t0007g0202others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3447+2170G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15371672 | ||||||
| chr1:15371788
|
A | G | 169 | a0001c0001t0002g0057a0001c0001t0013g0104a0001c0002t0018g0156others(166): Show | 169 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(166): Show |
intron_variant | MODIFIER | c.3447+2286A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15371788 | ||||||
| chr1:15371922
|
T | C | 27 | a0002c0003t0003g0133a0002c0003t0006g0064a0002c0003t0006g0069others(24): Show | 27 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.3447+2420T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15371922 | ||||||
| chr1:15372060
|
C | G | 48 | a0001c0001t0002g0057a0001c0010t0001g0182a0001c0013t0011g0266others(45): Show | 48 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.3448-2442C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15372060 | ||||||
| chr1:15372129
|
G | A | 1 | a0008c0044t0009g0223 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3448-2373G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15372129 | ||||||
| chr1:15372183
|
A | G | 3 | a0002c0003t0006g0157a0009c0011t0019g0144a0036c0121t0007g0201 | 3 | HG02486.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3448-2319A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15372183 | ||||||
| chr1:15372210
|
G | GGGAACGA others(5): Show |
1 | a0002c0007t0003g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3448-2289_3448-227 others(16): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | INFO_REALIGN_3_PRIME | chr1 | 15372210 | |||||
| chr1:15372513
|
G | GCACCCAC others(1): Show |
11 | a0001c0001t0002g0041a0001c0001t0008g0149a0001c0001t0008g0160others(8): Show | 11 | HG00558.hp2 HG02015.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.3448-1988_3448-198 others(12): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | INFO_REALIGN_3_PRIME | chr1 | 15372513 | |||||
| chr1:15372533
|
T | C | 1 | a0004c0004t0005g0164 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3448-1969T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15372533 | ||||||
| chr1:15372537
|
C | G | 1 | a0020c0111t0030g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3448-1965C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15372537 | ||||||
| chr1:15372621
|
G | A | 4 | a0002c0019t0027g0244a0012c0079t0027g0248a0016c0040t0021g0249others(1): Show | 4 | HG02572.hp2 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3448-1881G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15372621 | ||||||
| chr1:15372702
|
G | A | 6 | a0001c0001t0013g0104a0001c0002t0018g0156a0001c0002t0049g0101others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.3448-1800G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15372702 | ||||||
| chr1:15372729
|
G | A | 2 | a0001c0039t0001g0036a0001c0039t0001g0037 | 2 | HG03017.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.3448-1773G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15372729 | ||||||
| chr1:15372746
|
A | G | 2 | a0001c0002t0001g0080a0005c0016t0033g0271 | 2 | HG01123.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.3448-1756A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15372746 | ||||||
| chr1:15372831
|
G | C | 143 | a0001c0001t0002g0057a0002c0003t0003g0133a0002c0003t0003g0192others(140): Show | 143 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.3448-1671G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15372831 | ||||||
| chr1:15373069
|
G | A | 30 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0006g0062others(27): Show | 30 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.3448-1433G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15373069 | ||||||
| chr1:15373100
|
T | C | 2 | a0002c0003t0003g0192a0006c0014t0003g0224 | 2 | NA18982.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.3448-1402T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15373100 | ||||||
| chr1:15373148
|
A | G | 1 | a0001c0001t0002g0054 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.3448-1354A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15373148 | ||||||
| chr1:15373221
|
A | AAAAAGAC | 4 | a0001c0090t0048g0158a0003c0085t0055g0139a0040c0077t0037g0262others(1): Show | 4 | HG02258.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3448-1280_3448-127 others(11): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | INFO_REALIGN_3_PRIME | chr1 | 15373221 | |||||
| chr1:15373306
|
C | T | 4 | a0001c0090t0048g0158a0003c0085t0055g0139a0040c0077t0037g0262others(1): Show | 4 | HG02258.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3448-1196C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15373306 | ||||||
| chr1:15373307
|
G | A | 4 | a0001c0001t0002g0054a0001c0001t0008g0127a0001c0001t0008g0129others(1): Show | 4 | NA18964.hp1 NA18968.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.3448-1195G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15373307 | ||||||
| chr1:15373356
|
C | CAAAAAAT others(268): Show |
10 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.3448-1132_3448-113 others(279): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | INFO_REALIGN_3_PRIME | chr1 | 15373356 | |||||
| chr1:15373356
|
C | CAAAAAAT others(268): Show |
1 | a0004c0038t0014g0155 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3448-1132_3448-113 others(279): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | INFO_REALIGN_3_PRIME | chr1 | 15373356 | |||||
| chr1:15373426
|
C | T | 1 | a0002c0053t0020g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3448-1076C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15373426 | ||||||
| chr1:15373437
|
G | A | 1 | a0059c0104t0045g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3448-1065G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15373437 | ||||||
| chr1:15373486
|
T | A | 1 | a0032c0120t0034g0259 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3448-1016T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15373486 | ||||||
| chr1:15373509
|
C | CA | 138 | a0001c0001t0002g0057a0002c0003t0003g0133a0002c0003t0003g0192others(135): Show | 138 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.3448-981dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | INFO_REALIGN_3_PRIME | chr1 | 15373509 | |||||
| chr1:15373572
|
G | T | 1 | a0001c0001t0013g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.3448-930G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15373572 | ||||||
| chr1:15373608
|
C | T | 52 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0006g0062others(49): Show | 52 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.3448-894C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15373608 | ||||||
| chr1:15373617
|
C | T | 1 | a0012c0041t0003g0124 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3448-885C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15373617 | ||||||
| chr1:15373686
|
C | T | 2 | a0026c0031t0003g0252a0026c0031t0003g0253 | 2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.3448-816C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15373686 | ||||||
| chr1:15373761
|
C | A | 48 | a0001c0001t0002g0057a0002c0003t0004g0017a0002c0003t0004g0044others(45): Show | 48 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.3448-741C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15373761 | ||||||
| chr1:15373885
|
C | T | 1 | a0001c0010t0009g0207 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3448-617C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15373885 | ||||||
| chr1:15374203
|
C | G | 1 | a0016c0107t0003g0145 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3448-299C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15374203 | ||||||
| chr1:15374252
|
C | T | 1 | a0014c0110t0008g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3448-250C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15374252 | ||||||
| chr1:15374253
|
G | A | 12 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(9): Show | 12 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.3448-249G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15374253 | ||||||
| chr1:15374446
|
G | A | 23 | a0002c0018t0007g0140a0002c0018t0021g0247a0004c0087t0046g0121others(20): Show | 23 | HG00735.hp2 HG00738.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.3448-56G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 26/33 | chr1 | 15374446 | ||||||
| chr1:15374675
|
C | T | 1 | a0062c0062t0011g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3577+44C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15374675 | ||||||
| chr1:15374684
|
T | C | 11 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.3577+53T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15374684 | ||||||
| chr1:15374834
|
A | G | 3 | a0001c0001t0002g0070a0001c0001t0014g0052a0001c0036t0002g0055 | 3 | HG01928.hp2 HG01975.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.3577+203A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15374834 | ||||||
| chr1:15374848
|
G | GT | 7 | a0001c0013t0011g0266a0003c0006t0002g0090a0007c0012t0016g0256others(4): Show | 7 | HG02615.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.3577+228dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 15374848 | |||||
| chr1:15374853
|
T | TG | 12 | a0004c0038t0014g0155a0004c0087t0046g0121a0007c0033t0007g0138others(9): Show | 12 | HG02257.hp1 HG02280.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3577+222_3577+223i others(3): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15374853 | ||||||
| chr1:15374853
|
T | TGG | 7 | a0004c0004t0007g0001a0004c0004t0007g0002a0004c0038t0007g0143others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.3577+222_3577+223i others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15374853 | ||||||
| chr1:15374854
|
T | G | 101 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0004g0017others(98): Show | 101 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.3577+223T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15374854 | ||||||
| chr1:15374856
|
T | G | 10 | a0002c0019t0027g0244a0012c0079t0027g0248a0016c0040t0021g0249others(7): Show | 10 | HG01069.hp2 HG01167.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3577+225T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15374856 | ||||||
| chr1:15374857
|
T | G | 1 | a0003c0086t0009g0142 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3577+226T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15374857 | ||||||
| chr1:15374857
|
TTTG | T | 9 | a0002c0019t0027g0244a0012c0079t0027g0248a0016c0040t0021g0249others(6): Show | 9 | HG01069.hp2 HG01167.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3577+229_3577+231d others(5): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 15374857 | |||||
| chr1:15374858
|
T | G | 2 | a0003c0055t0012g0213a0005c0005t0015g0283 | 2 | NA18983.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.3577+227T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15374858 | ||||||
| chr1:15374858
|
TTG | T | 7 | a0002c0018t0018g0153a0018c0020t0022g0239a0018c0020t0022g0240others(4): Show | 7 | HG02965.hp2 HG03041.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.3577+229_3577+230d others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr1 | 15374858 | |||||
| chr1:15374859
|
T | G | 11 | a0001c0001t0057g0250a0001c0002t0001g0058a0001c0002t0001g0076others(8): Show | 11 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.3577+228T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15374859 | ||||||
| chr1:15374859
|
TG | T | 9 | a0001c0001t0002g0054a0001c0001t0013g0104a0001c0002t0018g0156others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.3577+229delG | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15374859 | ||||||
| chr1:15374860
|
G | C | 95 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0004g0017others(92): Show | 95 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.3577+229G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15374860 | ||||||
| chr1:15374860
|
G | T | 148 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(145): Show | 148 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.3577+229G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15374860 | ||||||
| chr1:15374861
|
T | G | 2 | a0003c0009t0028g0191a0035c0124t0029g0217 | 2 | NA18978.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.3577+230T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15374861 | ||||||
| chr1:15374863
|
TG | T | 94 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0004g0017others(91): Show | 94 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.3577+233delG | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15374863 | ||||||
| chr1:15374864
|
G | T | 54 | a0002c0003t0014g0151a0002c0018t0007g0140a0002c0018t0018g0153others(51): Show | 54 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.3577+233G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15374864 | ||||||
| chr1:15374868
|
T | G | 3 | a0001c0001t0013g0072a0001c0001t0013g0092a0005c0005t0015g0275 | 3 | HG00642.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3577+237T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15374868 | ||||||
| chr1:15374869
|
T | G | 9 | a0001c0008t0025g0112a0001c0008t0025g0113a0001c0013t0011g0266others(6): Show | 9 | HG01258.hp2 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.3577+238T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15374869 | ||||||
| chr1:15374871
|
T | G | 1 | a0003c0006t0002g0122 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3577+240T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15374871 | ||||||
| chr1:15374880
|
A | G | 2 | a0007c0059t0014g0167a0007c0101t0014g0119 | 2 | HG00735.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.3577+249A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15374880 | ||||||
| chr1:15375086
|
G | C | 7 | a0002c0018t0018g0153a0002c0080t0019g0181a0009c0011t0019g0144others(4): Show | 7 | HG02486.hp1 HG02896.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.3577+455G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15375086 | ||||||
| chr1:15375135
|
C | T | 3 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241 | 3 | HG02965.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3578-468C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15375135 | ||||||
| chr1:15375175
|
G | A | 14 | a0002c0003t0003g0133a0002c0003t0006g0062a0002c0003t0006g0083others(11): Show | 14 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(11): Show |
intron_variant | MODIFIER | c.3578-428G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15375175 | ||||||
| chr1:15375268
|
C | T | 1 | a0002c0035t0006g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3578-335C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15375268 | ||||||
| chr1:15375458
|
C | T | 5 | a0007c0012t0016g0187a0007c0012t0016g0256a0007c0012t0026g0245others(2): Show | 5 | HG02615.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.3578-145C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15375458 | ||||||
| chr1:15375460
|
A | G | 29 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(26): Show | 29 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.3578-143A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 27/33 | chr1 | 15375460 | ||||||
| chr1:15375732
|
TA | T | 4 | a0001c0090t0048g0158a0003c0085t0055g0139a0040c0077t0037g0262others(1): Show | 4 | HG02258.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.3705+4delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | INFO_REALIGN_3_PRIME | chr1 | 15375732 | |||||
| chr1:15375739
|
A | G | 4 | a0002c0018t0007g0140a0002c0018t0021g0247a0014c0112t0007g0202others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3705+9A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15375739 | ||||||
| chr1:15375801
|
T | G | 155 | a0001c0001t0002g0057a0002c0003t0003g0133a0002c0003t0003g0192others(152): Show | 155 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.3705+71T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15375801 | ||||||
| chr1:15375938
|
C | T | 13 | a0002c0035t0006g0026a0002c0035t0006g0031a0002c0053t0020g0096others(10): Show | 13 | HG00738.hp1 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.3705+208C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15375938 | ||||||
| chr1:15375980
|
G | C | 1 | a0005c0070t0035g0287 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3705+250G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15375980 | ||||||
| chr1:15376045
|
T | TTTTA | 3 | a0001c0015t0001g0111a0005c0005t0015g0280a0059c0104t0045g0014 | 3 | HG01361.hp1 HG01928.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3705+347_3705+350d others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | INFO_REALIGN_3_PRIME | chr1 | 15376045 | |||||
| chr1:15376065
|
ATTTATTT others(21): Show |
A | 1 | a0002c0035t0006g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3705+347_3705+374d others(30): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | INFO_REALIGN_3_PRIME | chr1 | 15376065 | |||||
| chr1:15376069
|
A | T | 1 | a0004c0087t0046g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3705+339A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376069 | ||||||
| chr1:15376069
|
ATTTATTT others(5): Show |
A | 23 | a0001c0090t0048g0158a0002c0035t0006g0026a0002c0053t0020g0096others(20): Show | 23 | HG00642.hp2 HG00738.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.3705+366_3705+377d others(14): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | INFO_REALIGN_3_PRIME | chr1 | 15376069 | |||||
| chr1:15376072
|
TATTTA | T | 7 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.3705+343_3705+347d others(7): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376072 | ||||||
| chr1:15376073
|
A | T | 2 | a0004c0087t0046g0121a0014c0118t0007g0198 | 2 | HG03579.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3705+343A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376073 | ||||||
| chr1:15376073
|
ATTTATTT others(1): Show |
A | 14 | a0001c0001t0015g0267a0001c0013t0011g0266a0001c0032t0014g0152others(11): Show | 14 | HG01070.hp1 HG01258.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.3705+351_3705+358d others(10): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | INFO_REALIGN_3_PRIME | chr1 | 15376073 | |||||
| chr1:15376073
|
ATTTATTT others(13): Show |
A | 47 | a0001c0001t0002g0057a0002c0003t0004g0017a0002c0003t0004g0044others(44): Show | 47 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.3705+351_3705+370d others(22): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | INFO_REALIGN_3_PRIME | chr1 | 15376073 | |||||
| chr1:15376075
|
TTATTTTT others(3): Show |
T | 3 | a0023c0130t0007g0238a0038c0129t0007g0235a0052c0088t0021g0242 | 3 | HG02622.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3705+347_3705+356d others(12): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | INFO_REALIGN_3_PRIME | chr1 | 15376075 | |||||
| chr1:15376077
|
A | T | 1 | a0004c0087t0046g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3705+347A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376077 | ||||||
| chr1:15376077
|
ATTTT | A | 85 | a0001c0001t0002g0049a0001c0001t0010g0281a0001c0001t0012g0128others(82): Show | 85 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.3705+351_3705+354d others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | INFO_REALIGN_3_PRIME | chr1 | 15376077 | |||||
| chr1:15376077
|
ATTTTTTT others(9): Show |
A | 33 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0006g0062others(30): Show | 33 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.3705+351_3705+366d others(18): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | INFO_REALIGN_3_PRIME | chr1 | 15376077 | |||||
| chr1:15376081
|
T | A | 72 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0054others(69): Show | 72 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.3705+351T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376081 | ||||||
| chr1:15376081
|
TTTTA | T | 5 | a0002c0018t0007g0140a0002c0018t0021g0247a0014c0112t0007g0202others(2): Show | 5 | HG02630.hp1 HG02723.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.3705+359_3705+362d others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | INFO_REALIGN_3_PRIME | chr1 | 15376081 | |||||
| chr1:15376084
|
TATTTA | T | 7 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.3705+355_3705+359d others(7): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376084 | ||||||
| chr1:15376085
|
A | T | 9 | a0001c0001t0002g0054a0004c0038t0014g0155a0004c0087t0046g0121others(6): Show | 9 | HG00642.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.3705+355A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376085 | ||||||
| chr1:15376089
|
A | T | 11 | a0001c0001t0002g0054a0001c0002t0001g0188a0003c0009t0001g0075others(8): Show | 11 | HG00621.hp2 HG00642.hp1 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.3705+359A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376089 | ||||||
| chr1:15376093
|
T | A | 19 | a0002c0035t0006g0026a0002c0053t0020g0096a0002c0081t0058g0251others(16): Show | 19 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.3705+363T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376093 | ||||||
| chr1:15376096
|
T | A | 1 | a0036c0121t0007g0201 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3705+366T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376096 | ||||||
| chr1:15376120
|
C | T | 3 | a0001c0032t0014g0152a0001c0032t0023g0282a0037c0128t0007g0233 | 3 | HG02622.hp1 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3705+390C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376120 | ||||||
| chr1:15376182
|
C | G | 1 | a0015c0023t0008g0130 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.3705+452C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376182 | ||||||
| chr1:15376250
|
C | T | 4 | a0002c0018t0007g0140a0002c0018t0021g0247a0014c0112t0007g0202others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3705+520C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376250 | ||||||
| chr1:15376339
|
C | G | 4 | a0001c0090t0048g0158a0003c0085t0055g0139a0040c0077t0037g0262others(1): Show | 4 | HG02258.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3705+609C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376339 | ||||||
| chr1:15376353
|
G | A | 7 | a0002c0018t0018g0153a0002c0080t0019g0181a0009c0011t0019g0144others(4): Show | 7 | HG02486.hp1 HG02896.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.3705+623G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376353 | ||||||
| chr1:15376385
|
C | T | 1 | a0001c0001t0002g0057 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.3705+655C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376385 | ||||||
| chr1:15376451
|
G | A | 1 | a0008c0125t0012g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3705+721G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376451 | ||||||
| chr1:15376491
|
C | T | 1 | a0044c0073t0011g0273 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.3705+761C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376491 | ||||||
| chr1:15376559
|
C | G | 3 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241 | 3 | HG02965.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3705+829C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376559 | ||||||
| chr1:15376572
|
C | T | 3 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241 | 3 | HG02965.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3705+842C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376572 | ||||||
| chr1:15376728
|
A | G | 2 | a0015c0023t0008g0123a0015c0023t0008g0131 | 2 | NA18977.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.3705+998A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376728 | ||||||
| chr1:15376778
|
A | G | 158 | a0001c0001t0002g0057a0001c0032t0014g0152a0001c0032t0023g0282others(155): Show | 158 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.3705+1048A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376778 | ||||||
| chr1:15376787
|
C | T | 4 | a0002c0019t0027g0244a0012c0079t0027g0248a0016c0040t0021g0249others(1): Show | 4 | HG02572.hp2 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3705+1057C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376787 | ||||||
| chr1:15376836
|
G | C | 4 | a0002c0003t0005g0177a0004c0004t0004g0024a0004c0004t0004g0027others(1): Show | 4 | NA18970.hp2 NA18978.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.3705+1106G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376836 | ||||||
| chr1:15376926
|
G | A | 6 | a0002c0018t0018g0153a0002c0080t0019g0181a0009c0011t0019g0144others(3): Show | 6 | HG02486.hp1 HG02896.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.3705+1196G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376926 | ||||||
| chr1:15376959
|
T | G | 1 | a0003c0009t0009g0178 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3705+1229T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376959 | ||||||
| chr1:15376995
|
C | G | 2 | a0001c0039t0001g0036a0001c0039t0001g0037 | 2 | HG03017.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.3705+1265C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15376995 | ||||||
| chr1:15377016
|
G | C | 1 | a0014c0110t0008g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3705+1286G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15377016 | ||||||
| chr1:15377053
|
T | C | 2 | a0002c0003t0006g0064a0006c0014t0003g0214 | 2 | HG02523.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.3705+1323T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15377053 | ||||||
| chr1:15377292
|
C | A | 150 | a0001c0001t0002g0057a0002c0003t0003g0133a0002c0003t0003g0192others(147): Show | 150 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.3705+1562C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15377292 | ||||||
| chr1:15377329
|
C | T | 1 | a0001c0002t0001g0023 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3705+1599C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15377329 | ||||||
| chr1:15377455
|
A | G | 2 | a0032c0120t0034g0259a0051c0100t0001g0091 | 2 | HG01069.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3705+1725A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15377455 | ||||||
| chr1:15377793
|
T | C | 4 | a0001c0002t0001g0188a0003c0009t0001g0075a0022c0046t0009g0193others(1): Show | 4 | HG00621.hp2 HG00673.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.3705+2063T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15377793 | ||||||
| chr1:15377812
|
A | G | 5 | a0002c0018t0007g0140a0002c0018t0021g0247a0014c0110t0008g0254others(2): Show | 5 | HG02572.hp1 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.3705+2082A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15377812 | ||||||
| chr1:15377889
|
T | G | 1 | a0050c0093t0018g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3705+2159T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15377889 | ||||||
| chr1:15377891
|
A | T | 1 | a0050c0093t0018g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3705+2161A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15377891 | ||||||
| chr1:15377935
|
A | G | 1 | a0022c0046t0009g0222 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3705+2205A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15377935 | ||||||
| chr1:15378028
|
G | T | 1 | a0002c0007t0006g0108 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3705+2298G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15378028 | ||||||
| chr1:15378042
|
G | A | 3 | a0001c0032t0014g0152a0001c0032t0023g0282a0037c0128t0007g0233 | 3 | HG02622.hp1 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3705+2312G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15378042 | ||||||
| chr1:15378057
|
A | G | 29 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(26): Show | 29 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.3705+2327A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15378057 | ||||||
| chr1:15378069
|
C | T | 6 | a0001c0010t0001g0182a0001c0013t0011g0266a0003c0098t0029g0237others(3): Show | 6 | HG01099.hp1 HG01258.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3705+2339C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15378069 | ||||||
| chr1:15378193
|
G | A | 41 | a0002c0003t0004g0017a0002c0003t0004g0044a0002c0003t0005g0135others(38): Show | 41 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.3705+2463G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15378193 | ||||||
| chr1:15378453
|
G | A | 11 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.3706-2248G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15378453 | ||||||
| chr1:15378512
|
G | A | 1 | a0039c0126t0019g0185 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3706-2189G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15378512 | ||||||
| chr1:15378535
|
G | A | 29 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(26): Show | 29 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.3706-2166G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15378535 | ||||||
| chr1:15378576
|
G | A | 41 | a0002c0003t0004g0017a0002c0003t0004g0044a0002c0003t0005g0135others(38): Show | 41 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.3706-2125G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15378576 | ||||||
| chr1:15378634
|
C | A | 12 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(9): Show | 12 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.3706-2067C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15378634 | ||||||
| chr1:15379064
|
T | G | 1 | a0010c0043t0005g0012 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3706-1637T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15379064 | ||||||
| chr1:15379093
|
CACAGAG | C | 11 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.3706-1604_3706-159 others(10): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | INFO_REALIGN_3_PRIME | chr1 | 15379093 | |||||
| chr1:15379142
|
G | A | 2 | a0006c0014t0005g0255a0057c0105t0004g0059 | 2 | HG00642.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.3706-1559G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15379142 | ||||||
| chr1:15379214
|
C | T | 3 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241 | 3 | HG02965.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3706-1487C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15379214 | ||||||
| chr1:15379316
|
A | C | 1 | a0003c0009t0001g0035 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3706-1385A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15379316 | ||||||
| chr1:15379575
|
T | G | 148 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0004g0017others(145): Show | 148 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.3706-1126T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15379575 | ||||||
| chr1:15379586
|
C | T | 3 | a0001c0032t0014g0152a0001c0032t0023g0282a0037c0128t0007g0233 | 3 | HG02622.hp1 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3706-1115C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15379586 | ||||||
| chr1:15379679
|
A | G | 12 | a0007c0012t0016g0187a0007c0012t0016g0256a0007c0012t0026g0245others(9): Show | 12 | HG02257.hp1 HG02486.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.3706-1022A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15379679 | ||||||
| chr1:15379763
|
A | G | 29 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(26): Show | 29 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.3706-938A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15379763 | ||||||
| chr1:15379796
|
T | C | 1 | a0001c0010t0001g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3706-905T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15379796 | ||||||
| chr1:15379853
|
G | A | 3 | a0001c0090t0048g0158a0003c0085t0055g0139a0040c0077t0037g0262 | 3 | HG03225.hp1 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3706-848G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15379853 | ||||||
| chr1:15379984
|
G | C | 1 | a0002c0053t0020g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3706-717G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15379984 | ||||||
| chr1:15380011
|
C | A | 29 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(26): Show | 29 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.3706-690C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15380011 | ||||||
| chr1:15380023
|
G | A | 3 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241 | 3 | HG02965.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3706-678G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15380023 | ||||||
| chr1:15380033
|
G | A | 41 | a0002c0003t0004g0017a0002c0003t0004g0044a0002c0003t0005g0135others(38): Show | 41 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.3706-668G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15380033 | ||||||
| chr1:15380044
|
G | A | 16 | a0002c0018t0018g0153a0002c0019t0027g0244a0002c0080t0019g0181others(13): Show | 16 | HG01069.hp2 HG01167.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.3706-657G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15380044 | ||||||
| chr1:15380212
|
C | G | 132 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0004g0017others(129): Show | 132 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.3706-489C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15380212 | ||||||
| chr1:15380255
|
G | T | 3 | a0002c0018t0018g0153a0002c0080t0019g0181a0039c0126t0019g0185 | 3 | HG02896.hp1 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3706-446G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15380255 | ||||||
| chr1:15380321
|
C | G | 3 | a0001c0001t0002g0070a0001c0001t0014g0052a0001c0036t0002g0055 | 3 | HG01928.hp2 HG01975.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.3706-380C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15380321 | ||||||
| chr1:15380331
|
G | C | 1 | a0001c0002t0031g0088 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3706-370G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15380331 | ||||||
| chr1:15380480
|
G | A | 1 | a0040c0077t0037g0262 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3706-221G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15380480 | ||||||
| chr1:15380599
|
C | G | 1 | a0004c0087t0046g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3706-102C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15380599 | ||||||
| chr1:15380615
|
C | T | 2 | a0012c0041t0003g0124a0012c0041t0003g0125 | 2 | HG01255.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.3706-86C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15380615 | ||||||
| chr1:15380616
|
G | A | 1 | a0033c0131t0005g0219 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3706-85G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15380616 | ||||||
| chr1:15380641
|
C | T | 41 | a0002c0003t0004g0017a0002c0003t0004g0044a0002c0003t0005g0135others(38): Show | 41 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.3706-60C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 28/33 | chr1 | 15380641 | ||||||
| chr1:15381078
|
T | C | 5 | a0001c0001t0002g0093a0001c0001t0002g0099a0001c0001t0013g0048others(2): Show | 5 | NA18943.hp2 NA18955.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.3802-153T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 29/33 | chr1 | 15381078 | ||||||
| chr1:15381168
|
T | G | 1 | a0014c0110t0008g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3802-63T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 29/33 | chr1 | 15381168 | ||||||
| chr1:15381192
|
G | T | 29 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(26): Show | 29 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.3802-39G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 29/33 | chr1 | 15381192 | ||||||
| chr1:15381218
|
G | A | 29 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(26): Show | 29 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.3802-13G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 29/33 | chr1 | 15381218 | ||||||
| chr1:15381488
|
G | A | 103 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0004g0017others(100): Show | 103 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.4022+37G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 30/33 | chr1 | 15381488 | ||||||
| chr1:15381500
|
T | C | 29 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(26): Show | 29 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.4022+49T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 30/33 | chr1 | 15381500 | ||||||
| chr1:15381529
|
C | T | 29 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(26): Show | 29 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.4022+78C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 30/33 | chr1 | 15381529 | ||||||
| chr1:15381530
|
T | C | 29 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(26): Show | 29 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.4022+79T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 30/33 | chr1 | 15381530 | ||||||
| chr1:15381592
|
C | A | 29 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(26): Show | 29 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.4022+141C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 30/33 | chr1 | 15381592 | ||||||
| chr1:15381708
|
C | T | 1 | a0002c0053t0020g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4022+257C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 30/33 | chr1 | 15381708 | ||||||
| chr1:15381722
|
T | C | 1 | a0014c0110t0008g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4022+271T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 30/33 | chr1 | 15381722 | ||||||
| chr1:15381724
|
G | A | 9 | a0002c0019t0027g0244a0012c0079t0027g0248a0016c0040t0021g0249others(6): Show | 9 | HG01069.hp2 HG01167.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.4022+273G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 30/33 | chr1 | 15381724 | ||||||
| chr1:15381742
|
AT | A | 95 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0004g0017others(92): Show | 95 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.4023-284delT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 30/33 | INFO_REALIGN_3_PRIME | chr1 | 15381742 | |||||
| chr1:15381778
|
C | T | 1 | a0020c0116t0052g0200 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4023-250C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 30/33 | chr1 | 15381778 | ||||||
| chr1:15381844
|
C | G | 5 | a0007c0033t0007g0138a0007c0033t0014g0068a0007c0059t0014g0167others(2): Show | 5 | HG00735.hp2 HG00738.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.4023-184C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 30/33 | chr1 | 15381844 | ||||||
| chr1:15381888
|
G | A | 11 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.4023-140G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 30/33 | chr1 | 15381888 | ||||||
| chr1:15381929
|
C | T | 1 | a0001c0002t0009g0162 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4023-99C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 30/33 | chr1 | 15381929 | ||||||
| chr1:15381958
|
G | A | 1 | a0032c0120t0034g0259 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4023-70G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 30/33 | chr1 | 15381958 | ||||||
| chr1:15381960
|
G | T | 1 | a0019c0022t0018g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4023-68G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 30/33 | chr1 | 15381960 | ||||||
| chr1:15382005
|
C | T | 1 | a0001c0002t0001g0025 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.4023-23C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 30/33 | chr1 | 15382005 | ||||||
| chr1:15382021
|
C | A | 1 | a0059c0104t0045g0014 | 1 | HG02559.hp1 | splice_region_variant&intron_variant | LOW | c.4023-7C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 30/33 | chr1 | 15382021 | ||||||
| chr1:15382220
|
C | A | 29 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(26): Show | 29 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.4188+27C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15382220 | ||||||
| chr1:15382271
|
G | C | 29 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(26): Show | 29 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.4188+78G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15382271 | ||||||
| chr1:15382328
|
C | G | 1 | a0020c0116t0052g0200 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4188+135C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15382328 | ||||||
| chr1:15382369
|
C | A | 1 | a0059c0104t0045g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4188+176C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15382369 | ||||||
| chr1:15382402
|
C | T | 1 | a0057c0105t0004g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4188+209C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15382402 | ||||||
| chr1:15382429
|
G | C | 6 | a0001c0001t0012g0126a0001c0001t0012g0128a0001c0001t0013g0072others(3): Show | 6 | HG00642.hp1 HG01106.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.4188+236G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15382429 | ||||||
| chr1:15382504
|
G | C | 29 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(26): Show | 29 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.4188+311G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15382504 | ||||||
| chr1:15382543
|
G | A | 2 | a0004c0004t0004g0029a0004c0004t0004g0030 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.4188+350G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15382543 | ||||||
| chr1:15382621
|
T | C | 3 | a0029c0114t0056g0199a0047c0089t0050g0105a0060c0065t0043g0005 | 3 | HG01167.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4188+428T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15382621 | ||||||
| chr1:15382632
|
G | C | 29 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(26): Show | 29 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.4188+439G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15382632 | ||||||
| chr1:15382811
|
G | A | 34 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(31): Show | 34 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.4188+618G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15382811 | ||||||
| chr1:15382825
|
G | C | 4 | a0002c0018t0007g0140a0002c0018t0021g0247a0014c0112t0007g0202others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.4188+632G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15382825 | ||||||
| chr1:15382856
|
G | A | 30 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0006g0062others(27): Show | 30 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.4188+663G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15382856 | ||||||
| chr1:15382867
|
C | T | 1 | a0032c0120t0034g0259 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4188+674C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15382867 | ||||||
| chr1:15382881
|
G | A | 5 | a0029c0114t0056g0199a0032c0120t0034g0259a0047c0089t0050g0105others(2): Show | 5 | HG01069.hp2 HG01167.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.4188+688G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15382881 | ||||||
| chr1:15382898
|
G | C | 41 | a0002c0003t0004g0017a0002c0003t0004g0044a0002c0003t0005g0135others(38): Show | 41 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.4188+705G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15382898 | ||||||
| chr1:15383009
|
C | G | 1 | a0009c0028t0011g0290 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.4188+816C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383009 | ||||||
| chr1:15383020
|
A | G | 34 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(31): Show | 34 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.4188+827A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383020 | ||||||
| chr1:15383024
|
G | A | 3 | a0021c0113t0016g0194a0021c0117t0016g0234a0059c0104t0045g0014 | 3 | HG02559.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.4188+831G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383024 | ||||||
| chr1:15383057
|
AC | A | 34 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(31): Show | 34 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.4188+865delC | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383057 | ||||||
| chr1:15383059
|
A | G | 95 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0004g0017others(92): Show | 95 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.4188+866A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383059 | ||||||
| chr1:15383145
|
T | C | 5 | a0029c0114t0056g0199a0032c0120t0034g0259a0047c0089t0050g0105others(2): Show | 5 | HG01069.hp2 HG01167.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.4188+952T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383145 | ||||||
| chr1:15383298
|
G | A | 2 | a0001c0001t0013g0072a0001c0001t0013g0092 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.4188+1105G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383298 | ||||||
| chr1:15383336
|
C | T | 34 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(31): Show | 34 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.4188+1143C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383336 | ||||||
| chr1:15383346
|
C | T | 1 | a0002c0080t0019g0181 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4188+1153C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383346 | ||||||
| chr1:15383479
|
C | T | 16 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(13): Show | 16 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.4188+1286C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383479 | ||||||
| chr1:15383560
|
C | T | 2 | a0006c0014t0005g0255a0057c0105t0004g0059 | 2 | HG00642.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.4188+1367C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383560 | ||||||
| chr1:15383617
|
C | G | 95 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0004g0017others(92): Show | 95 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.4188+1424C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383617 | ||||||
| chr1:15383730
|
C | T | 34 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(31): Show | 34 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.4188+1537C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383730 | ||||||
| chr1:15383746
|
G | A | 1 | a0014c0110t0008g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4188+1553G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383746 | ||||||
| chr1:15383836
|
A | G | 1 | a0005c0005t0015g0286 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4188+1643A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383836 | ||||||
| chr1:15383884
|
C | A | 1 | a0059c0104t0045g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4188+1691C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383884 | ||||||
| chr1:15383885
|
C | T | 1 | a0059c0104t0045g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4188+1692C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383885 | ||||||
| chr1:15383915
|
G | C | 153 | a0001c0090t0048g0158a0002c0003t0003g0133a0002c0003t0003g0192others(150): Show | 153 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.4188+1722G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383915 | ||||||
| chr1:15383983
|
T | G | 1 | a0012c0079t0027g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4188+1790T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383983 | ||||||
| chr1:15383997
|
CAT | C | 76 | a0002c0003t0004g0017a0002c0003t0004g0044a0002c0003t0005g0135others(73): Show | 76 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.4188+1805_4188+180 others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383997 | ||||||
| chr1:15383998
|
A | G | 1 | a0004c0087t0046g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4188+1805A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15383998 | ||||||
| chr1:15384017
|
CAT | C | 34 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(31): Show | 34 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.4188+1825_4188+182 others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15384017 | ||||||
| chr1:15384093
|
C | G | 1 | a0004c0087t0046g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4188+1900C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15384093 | ||||||
| chr1:15384233
|
T | C | 34 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(31): Show | 34 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.4188+2040T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15384233 | ||||||
| chr1:15384417
|
G | A | 3 | a0025c0042t0003g0010a0025c0042t0003g0011a0062c0062t0011g0285 | 3 | HG01069.hp1 HG01071.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.4188+2224G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15384417 | ||||||
| chr1:15384446
|
C | T | 4 | a0002c0018t0007g0140a0002c0018t0021g0247a0014c0112t0007g0202others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.4188+2253C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15384446 | ||||||
| chr1:15384557
|
T | A | 17 | a0007c0012t0016g0187a0007c0012t0016g0256a0007c0012t0026g0245others(14): Show | 17 | HG00735.hp2 HG00738.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.4188+2364T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15384557 | ||||||
| chr1:15384576
|
G | A | 1 | a0059c0104t0045g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4188+2383G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15384576 | ||||||
| chr1:15384630
|
C | G | 137 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0004g0017others(134): Show | 137 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.4188+2437C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15384630 | ||||||
| chr1:15384821
|
C | T | 1 | a0032c0120t0034g0259 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4188+2628C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15384821 | ||||||
| chr1:15384867
|
A | G | 140 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0004g0017others(137): Show | 140 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.4188+2674A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15384867 | ||||||
| chr1:15384875
|
G | A | 34 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(31): Show | 34 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.4188+2682G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15384875 | ||||||
| chr1:15384942
|
C | T | 8 | a0002c0003t0053g0176a0004c0004t0004g0074a0004c0004t0004g0086others(5): Show | 8 | HG00438.hp2 HG00673.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.4188+2749C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15384942 | ||||||
| chr1:15384979
|
A | G | 34 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(31): Show | 34 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.4188+2786A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15384979 | ||||||
| chr1:15384989
|
C | T | 1 | a0033c0131t0005g0219 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4188+2796C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15384989 | ||||||
| chr1:15384991
|
T | C | 147 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0004g0017others(144): Show | 147 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.4188+2798T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15384991 | ||||||
| chr1:15385027
|
C | G | 34 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(31): Show | 34 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.4188+2834C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15385027 | ||||||
| chr1:15385071
|
G | T | 1 | a0016c0040t0021g0249 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4188+2878G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15385071 | ||||||
| chr1:15385113
|
G | A | 1 | a0019c0022t0004g0071 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.4188+2920G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15385113 | ||||||
| chr1:15385118
|
A | AAAG | 135 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0004g0017others(132): Show | 135 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.4188+2925_4188+292 others(7): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15385118 | ||||||
| chr1:15385129
|
CT | C | 112 | a0001c0032t0014g0152a0001c0032t0023g0282a0001c0090t0048g0158others(109): Show | 112 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.4189-2907delT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr1 | 15385129 | |||||
| chr1:15385129
|
CTT | C | 35 | a0002c0003t0006g0083a0002c0003t0014g0151a0004c0004t0007g0001others(32): Show | 35 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.4189-2908_4189-290 others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr1 | 15385129 | |||||
| chr1:15385144
|
T | G | 34 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(31): Show | 34 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.4189-2907T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15385144 | ||||||
| chr1:15385156
|
A | G | 34 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(31): Show | 34 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.4189-2895A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15385156 | ||||||
| chr1:15385299
|
CAA | C | 4 | a0009c0011t0019g0144a0019c0022t0018g0015a0023c0127t0019g0184others(1): Show | 4 | HG02486.hp1 HG03471.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.4189-2750_4189-274 others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr1 | 15385299 | |||||
| chr1:15385529
|
T | C | 34 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(31): Show | 34 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.4189-2522T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15385529 | ||||||
| chr1:15385683
|
G | A | 34 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(31): Show | 34 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.4189-2368G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15385683 | ||||||
| chr1:15385719
|
A | G | 2 | a0001c0001t0012g0161a0003c0006t0008g0134 | 2 | HG02602.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.4189-2332A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15385719 | ||||||
| chr1:15385730
|
G | C | 11 | a0002c0018t0018g0153a0002c0019t0027g0244a0002c0080t0019g0181others(8): Show | 11 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.4189-2321G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15385730 | ||||||
| chr1:15385733
|
C | A | 52 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0006g0062others(49): Show | 52 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.4189-2318C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15385733 | ||||||
| chr1:15385741
|
CT | C | 8 | a0002c0018t0007g0140a0002c0018t0021g0247a0014c0110t0008g0254others(5): Show | 8 | HG02572.hp1 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.4189-2309delT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15385741 | ||||||
| chr1:15385960
|
A | G | 1 | a0059c0104t0045g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4189-2091A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15385960 | ||||||
| chr1:15386165
|
C | T | 4 | a0001c0090t0048g0158a0003c0085t0055g0139a0040c0077t0037g0262others(1): Show | 4 | HG02258.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4189-1886C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15386165 | ||||||
| chr1:15386279
|
C | T | 3 | a0025c0042t0003g0010a0025c0042t0003g0011a0062c0062t0011g0285 | 3 | HG01069.hp1 HG01071.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.4189-1772C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15386279 | ||||||
| chr1:15386389
|
C | A | 153 | a0001c0090t0048g0158a0002c0003t0003g0133a0002c0003t0003g0192others(150): Show | 153 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.4189-1662C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15386389 | ||||||
| chr1:15386495
|
C | T | 1 | a0001c0092t0002g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4189-1556C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15386495 | ||||||
| chr1:15386678
|
C | T | 3 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241 | 3 | HG02965.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.4189-1373C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15386678 | ||||||
| chr1:15386811
|
C | G | 16 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(13): Show | 16 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.4189-1240C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15386811 | ||||||
| chr1:15386826
|
T | C | 1 | a0058c0106t0004g0042 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.4189-1225T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15386826 | ||||||
| chr1:15386832
|
T | C | 1 | a0058c0106t0004g0042 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.4189-1219T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15386832 | ||||||
| chr1:15386849
|
C | CT | 96 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0004g0017others(93): Show | 96 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.4189-1191dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr1 | 15386849 | |||||
| chr1:15386849
|
C | CTT | 14 | a0001c0002t0018g0156a0001c0002t0049g0101a0002c0003t0005g0172others(11): Show | 14 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.4189-1192_4189-119 others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr1 | 15386849 | |||||
| chr1:15386849
|
C | CTTT | 31 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(28): Show | 31 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.4189-1193_4189-119 others(7): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr1 | 15386849 | |||||
| chr1:15386861
|
G | T | 1 | a0004c0087t0046g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4189-1190G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15386861 | ||||||
| chr1:15386919
|
G | A | 1 | a0004c0004t0005g0174 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.4189-1132G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15386919 | ||||||
| chr1:15387020
|
C | T | 4 | a0002c0081t0058g0251a0026c0031t0003g0252a0026c0031t0003g0253others(1): Show | 4 | HG02055.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4189-1031C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15387020 | ||||||
| chr1:15387180
|
C | T | 5 | a0007c0033t0007g0138a0007c0033t0014g0068a0007c0059t0014g0167others(2): Show | 5 | HG00735.hp2 HG00738.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.4189-871C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15387180 | ||||||
| chr1:15387244
|
T | C | 150 | a0001c0002t0018g0156a0001c0002t0049g0101a0002c0003t0003g0133others(147): Show | 150 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.4189-807T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15387244 | ||||||
| chr1:15387307
|
T | C | 17 | a0007c0012t0016g0187a0007c0012t0016g0256a0007c0012t0026g0245others(14): Show | 17 | HG00735.hp2 HG00738.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.4189-744T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15387307 | ||||||
| chr1:15387339
|
A | T | 3 | a0001c0032t0014g0152a0001c0032t0023g0282a0037c0128t0007g0233 | 3 | HG02622.hp1 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.4189-712A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15387339 | ||||||
| chr1:15387405
|
A | G | 3 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241 | 3 | HG02965.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.4189-646A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15387405 | ||||||
| chr1:15387422
|
G | A | 52 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0006g0062others(49): Show | 52 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.4189-629G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15387422 | ||||||
| chr1:15387514
|
C | T | 17 | a0007c0012t0016g0187a0007c0012t0016g0256a0007c0012t0026g0245others(14): Show | 17 | HG00735.hp2 HG00738.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.4189-537C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15387514 | ||||||
| chr1:15387660
|
G | A | 34 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(31): Show | 34 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.4189-391G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15387660 | ||||||
| chr1:15387747
|
T | G | 1 | a0058c0106t0004g0042 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.4189-304T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15387747 | ||||||
| chr1:15387748
|
G | T | 1 | a0058c0106t0004g0042 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.4189-303G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15387748 | ||||||
| chr1:15387762
|
G | A | 1 | a0002c0018t0007g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4189-289G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15387762 | ||||||
| chr1:15387834
|
A | G | 34 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(31): Show | 34 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.4189-217A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15387834 | ||||||
| chr1:15387936
|
C | T | 1 | a0001c0010t0001g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4189-115C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 31/33 | chr1 | 15387936 | ||||||
| chr1:15388220
|
G | A | 41 | a0002c0003t0004g0017a0002c0003t0004g0044a0002c0003t0005g0135others(38): Show | 41 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.4269+89G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15388220 | ||||||
| chr1:15388278
|
T | A | 155 | a0001c0002t0018g0156a0001c0002t0049g0101a0001c0090t0048g0158others(152): Show | 155 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.4269+147T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15388278 | ||||||
| chr1:15388313
|
G | C | 293 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(290): Show | 293 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(290): Show |
intron_variant | MODIFIER | c.4269+182G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15388313 | ||||||
| chr1:15388335
|
C | CCCCTCCC others(189): Show |
1 | a0004c0087t0046g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4269+214_4269+215i others(198): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(173): Show |
17 | a0007c0012t0016g0187a0007c0012t0016g0256a0007c0012t0026g0245others(14): Show | 17 | HG00735.hp2 HG00738.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.4269+214_4269+215i others(182): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(189): Show |
3 | a0029c0114t0056g0199a0047c0089t0050g0105a0060c0065t0043g0005 | 3 | HG01167.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4269+214_4269+215i others(198): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(185): Show |
1 | a0032c0120t0034g0259 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4269+214_4269+215i others(194): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(181): Show |
1 | a0051c0100t0001g0091 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.4269+214_4269+215i others(190): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(177): Show |
10 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.4269+214_4269+215i others(186): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(176): Show |
1 | a0052c0088t0021g0242 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4269+214_4269+215i others(185): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(251): Show |
4 | a0009c0011t0019g0144a0019c0022t0018g0015a0023c0127t0019g0184others(1): Show | 4 | HG02486.hp1 HG03471.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.4269+214_4269+215i others(260): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(288): Show |
3 | a0002c0018t0018g0153a0002c0080t0019g0181a0039c0126t0019g0185 | 3 | HG02896.hp1 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4269+214_4269+215i others(297): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(116): Show |
52 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0006g0062others(49): Show | 52 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.4269+214_4269+215i others(125): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(174): Show |
1 | a0019c0022t0004g0071 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.4269+214_4269+215i others(183): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(103): Show |
7 | a0001c0001t0012g0126a0001c0001t0012g0128a0001c0001t0013g0072others(4): Show | 7 | HG01106.hp2 HG01192.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.4269+214_4269+215i others(112): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(140): Show |
1 | a0059c0104t0045g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4269+214_4269+215i others(149): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(99): Show |
121 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(118): Show | 121 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.4269+214_4269+215i others(108): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(136): Show |
3 | a0001c0032t0014g0152a0001c0032t0023g0282a0037c0128t0007g0233 | 3 | HG02622.hp1 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.4269+214_4269+215i others(145): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(173): Show |
1 | a0058c0106t0004g0042 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.4269+214_4269+215i others(182): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(173): Show |
38 | a0002c0003t0004g0017a0002c0003t0004g0044a0002c0003t0005g0135others(35): Show | 38 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.4269+214_4269+215i others(182): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(95): Show |
5 | a0001c0001t0013g0104a0001c0102t0012g0146a0003c0086t0009g0142others(2): Show | 5 | HG01070.hp1 HG01109.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.4269+214_4269+215i others(104): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(206): Show |
6 | a0001c0002t0018g0156a0001c0002t0049g0101a0002c0019t0027g0244others(3): Show | 6 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.4269+214_4269+215i others(215): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(87): Show |
2 | a0001c0010t0001g0097a0001c0010t0001g0098 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.4269+214_4269+215i others(96): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(123): Show |
4 | a0001c0090t0048g0158a0003c0085t0055g0139a0040c0077t0037g0262others(1): Show | 4 | HG02258.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4269+214_4269+215i others(132): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(157): Show |
10 | a0002c0018t0007g0140a0002c0018t0021g0247a0006c0014t0005g0255others(7): Show | 10 | HG00642.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.4269+214_4269+215i others(166): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388335
|
C | CCCCTCCC others(176): Show |
1 | a0004c0004t0004g0024 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.4269+212_4269+213i others(185): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15388335 | |||||
| chr1:15388346
|
G | C | 150 | a0001c0002t0018g0156a0001c0002t0049g0101a0002c0003t0003g0133others(147): Show | 150 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.4269+215G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15388346 | ||||||
| chr1:15388363
|
T | C | 10 | a0002c0018t0007g0140a0002c0018t0021g0247a0006c0014t0005g0255others(7): Show | 10 | HG00642.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.4269+232T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15388363 | ||||||
| chr1:15388369
|
T | A | 4 | a0002c0018t0007g0140a0002c0018t0021g0247a0014c0112t0007g0202others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.4269+238T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15388369 | ||||||
| chr1:15388397
|
G | A | 13 | a0001c0002t0018g0156a0001c0002t0049g0101a0002c0018t0018g0153others(10): Show | 13 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.4269+266G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15388397 | ||||||
| chr1:15388576
|
T | G | 1 | a0001c0001t0002g0081 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.4269+445T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15388576 | ||||||
| chr1:15388577
|
G | A | 1 | a0004c0087t0046g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4269+446G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15388577 | ||||||
| chr1:15388657
|
C | T | 17 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(14): Show | 17 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.4269+526C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15388657 | ||||||
| chr1:15388705
|
C | T | 4 | a0002c0018t0007g0140a0002c0018t0021g0247a0014c0112t0007g0202others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.4269+574C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15388705 | ||||||
| chr1:15388771
|
T | C | 155 | a0001c0002t0018g0156a0001c0002t0049g0101a0001c0090t0048g0158others(152): Show | 155 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.4269+640T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15388771 | ||||||
| chr1:15388918
|
C | T | 4 | a0001c0090t0048g0158a0003c0085t0055g0139a0040c0077t0037g0262others(1): Show | 4 | HG02258.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4269+787C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15388918 | ||||||
| chr1:15388966
|
G | A | 7 | a0002c0018t0018g0153a0002c0080t0019g0181a0009c0011t0019g0144others(4): Show | 7 | HG02486.hp1 HG02896.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.4269+835G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15388966 | ||||||
| chr1:15389194
|
C | T | 3 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241 | 3 | HG02965.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.4269+1063C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15389194 | ||||||
| chr1:15389271
|
C | T | 158 | a0001c0002t0018g0156a0001c0002t0049g0101a0001c0032t0014g0152others(155): Show | 158 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.4269+1140C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15389271 | ||||||
| chr1:15389272
|
C | T | 1 | a0003c0037t0001g0032 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4269+1141C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15389272 | ||||||
| chr1:15389387
|
G | A | 3 | a0002c0019t0004g0118a0010c0043t0005g0012a0010c0043t0005g0013 | 3 | HG01261.hp2 HG01433.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.4269+1256G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15389387 | ||||||
| chr1:15389407
|
C | T | 3 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241 | 3 | HG02965.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.4269+1276C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15389407 | ||||||
| chr1:15389447
|
C | CA | 27 | a0001c0001t0002g0040a0001c0001t0002g0093a0001c0001t0010g0281others(24): Show | 27 | HG00544.hp2 HG00609.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.4269+1337dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAA | 8 | a0007c0012t0016g0256a0007c0012t0026g0246a0007c0033t0014g0068others(5): Show | 8 | HG00738.hp2 HG02615.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.4269+1335_4269+133 others(7): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAA | 11 | a0007c0033t0007g0138a0007c0059t0014g0167a0011c0025t0003g0211others(8): Show | 11 | HG00438.hp1 HG00558.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.4269+1334_4269+133 others(8): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA | 10 | a0002c0035t0006g0026a0002c0035t0006g0031a0002c0053t0020g0096others(7): Show | 10 | HG01074.hp2 HG01099.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.4269+1331_4269+133 others(11): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(1): Show |
8 | a0004c0058t0006g0183a0019c0022t0004g0022a0024c0027t0024g0258others(5): Show | 8 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.4269+1330_4269+133 others(12): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(5): Show |
2 | a0012c0041t0003g0124a0012c0041t0003g0125 | 2 | HG01255.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.4269+1326_4269+133 others(16): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(7): Show |
1 | a0066c0061t0042g0007 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4269+1324_4269+133 others(18): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(8): Show |
1 | a0067c0049t0005g0236 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.4269+1323_4269+133 others(19): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(9): Show |
3 | a0001c0090t0048g0158a0004c0004t0004g0116a0040c0077t0037g0262 | 3 | HG03225.hp1 HG03540.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.4269+1322_4269+133 others(20): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(10): Show |
5 | a0002c0003t0005g0172a0002c0007t0006g0115a0002c0134t0003g0209others(2): Show | 5 | HG01074.hp1 HG01515.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.4269+1321_4269+133 others(21): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(11): Show |
5 | a0004c0004t0004g0067a0010c0029t0017g0276a0010c0043t0005g0012others(2): Show | 5 | HG01255.hp1 HG01433.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.4269+1320_4269+133 others(22): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(12): Show |
8 | a0002c0003t0004g0044a0002c0080t0019g0181a0004c0004t0004g0073others(5): Show | 8 | HG01069.hp2 HG01081.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.4269+1319_4269+133 others(23): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(13): Show |
11 | a0002c0003t0053g0176a0002c0007t0005g0210a0002c0018t0007g0140others(8): Show | 11 | HG00423.hp2 HG00609.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.4269+1318_4269+133 others(24): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(14): Show |
8 | a0004c0004t0004g0074a0004c0004t0005g0174a0004c0057t0005g0189others(5): Show | 8 | HG00438.hp2 HG00673.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.4269+1317_4269+133 others(25): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(15): Show |
2 | a0002c0003t0005g0177a0004c0004t0004g0027 | 2 | NA18970.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.4269+1337_4269+133 others(26): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(16): Show |
6 | a0004c0004t0004g0024a0004c0004t0004g0030a0004c0004t0004g0086others(3): Show | 6 | HG01169.hp2 HG03927.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.4269+1337_4269+133 others(27): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(17): Show |
4 | a0002c0007t0005g0212a0004c0004t0004g0029a0006c0014t0005g0220others(1): Show | 4 | HG01167.hp2 HG02738.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.4269+1337_4269+133 others(28): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(18): Show |
5 | a0002c0003t0005g0135a0002c0018t0021g0247a0036c0121t0007g0201others(2): Show | 5 | HG01106.hp1 HG02723.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.4269+1337_4269+133 others(29): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(19): Show |
4 | a0004c0004t0005g0173a0004c0038t0014g0155a0028c0109t0007g0197others(1): Show | 4 | HG03209.hp2 HG03516.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.4269+1337_4269+133 others(30): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(20): Show |
1 | a0038c0129t0007g0235 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4269+1337_4269+133 others(31): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(21): Show |
7 | a0002c0003t0006g0064a0002c0003t0006g0069a0002c0003t0006g0089others(4): Show | 7 | HG02055.hp1 HG02523.hp2 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.4269+1337_4269+133 others(32): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(22): Show |
1 | a0002c0003t0004g0017 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4269+1337_4269+133 others(33): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(23): Show |
6 | a0002c0003t0003g0192a0002c0007t0003g0190a0004c0004t0005g0164others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.4269+1337_4269+133 others(34): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(24): Show |
3 | a0006c0014t0003g0224a0023c0130t0007g0238a0025c0042t0003g0010 | 3 | HG01069.hp1 NA18906.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.4269+1337_4269+133 others(35): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(25): Show |
3 | a0002c0007t0006g0108a0025c0042t0003g0011a0062c0062t0011g0285 | 3 | HG01071.hp2 HG01975.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.4269+1337_4269+133 others(36): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(26): Show |
1 | a0009c0011t0011g0272 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.4269+1337_4269+133 others(37): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(27): Show |
1 | a0002c0003t0003g0133 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.4269+1337_4269+133 others(38): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(28): Show |
2 | a0002c0003t0006g0062a0010c0074t0011g0261 | 2 | HG01109.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.4269+1337_4269+133 others(39): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
C | CAAAAAAA others(32): Show |
1 | a0006c0045t0003g0225 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.4269+1337_4269+133 others(43): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389447
|
CA | C | 7 | a0001c0002t0001g0038a0003c0006t0002g0046a0003c0009t0001g0075others(4): Show | 7 | HG00621.hp1 HG00621.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.4269+1337delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389447 | |||||
| chr1:15389460
|
A | AAAAAACA others(8): Show |
1 | a0004c0087t0046g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4269+1334_4269+133 others(19): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389460 | |||||
| chr1:15389599
|
GC | G | 11 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.4269+1470delC | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15389599 | |||||
| chr1:15389669
|
G | T | 3 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241 | 3 | HG02965.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.4269+1538G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15389669 | ||||||
| chr1:15389680
|
C | T | 4 | a0001c0090t0048g0158a0003c0085t0055g0139a0040c0077t0037g0262others(1): Show | 4 | HG02258.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4270-1530C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15389680 | ||||||
| chr1:15389681
|
G | A | 2 | a0001c0039t0001g0036a0001c0039t0001g0037 | 2 | HG03017.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.4270-1529G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15389681 | ||||||
| chr1:15389776
|
A | T | 1 | a0058c0106t0004g0042 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.4270-1434A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15389776 | ||||||
| chr1:15389777
|
T | A | 1 | a0058c0106t0004g0042 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.4270-1433T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15389777 | ||||||
| chr1:15389827
|
G | T | 1 | a0024c0027t0024g0288 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4270-1383G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15389827 | ||||||
| chr1:15389856
|
G | A | 7 | a0002c0018t0018g0153a0002c0080t0019g0181a0009c0011t0019g0144others(4): Show | 7 | HG02486.hp1 HG02896.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.4270-1354G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15389856 | ||||||
| chr1:15389990
|
C | T | 52 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0006g0062others(49): Show | 52 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.4270-1220C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15389990 | ||||||
| chr1:15390336
|
C | T | 4 | a0001c0090t0048g0158a0003c0085t0055g0139a0040c0077t0037g0262others(1): Show | 4 | HG02258.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4270-874C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15390336 | ||||||
| chr1:15390344
|
C | CA | 18 | a0001c0001t0002g0054a0001c0001t0002g0057a0001c0001t0008g0129others(15): Show | 18 | HG00423.hp1 HG00735.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.4270-843dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15390344 | |||||
| chr1:15390344
|
C | CAA | 8 | a0007c0033t0014g0068a0007c0082t0016g0180a0017c0017t0007g0008others(5): Show | 8 | HG02280.hp2 HG02486.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.4270-844_4270-843d others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15390344 | |||||
| chr1:15390344
|
C | CAAA | 8 | a0007c0012t0016g0187a0007c0012t0016g0256a0007c0012t0026g0245others(5): Show | 8 | HG02257.hp1 HG02615.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.4270-845_4270-843d others(5): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15390344 | |||||
| chr1:15390344
|
CA | C | 55 | a0001c0002t0018g0156a0001c0002t0049g0101a0001c0032t0014g0152others(52): Show | 55 | HG00642.hp2 HG00738.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.4270-843delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15390344 | |||||
| chr1:15390344
|
CAA | C | 39 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0006g0062others(36): Show | 39 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.4270-844_4270-843d others(4): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15390344 | |||||
| chr1:15390344
|
CAAA | C | 34 | a0002c0003t0004g0044a0002c0003t0005g0135a0002c0003t0005g0172others(31): Show | 34 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.4270-845_4270-843d others(5): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15390344 | |||||
| chr1:15390344
|
CAAAAAAA others(4): Show |
C | 1 | a0059c0104t0045g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4270-853_4270-843d others(13): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | INFO_REALIGN_3_PRIME | chr1 | 15390344 | |||||
| chr1:15390383
|
T | A | 4 | a0002c0081t0058g0251a0026c0031t0003g0252a0026c0031t0003g0253others(1): Show | 4 | HG02055.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4270-827T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15390383 | ||||||
| chr1:15390519
|
C | G | 3 | a0025c0042t0003g0010a0025c0042t0003g0011a0062c0062t0011g0285 | 3 | HG01069.hp1 HG01071.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.4270-691C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15390519 | ||||||
| chr1:15390646
|
T | C | 1 | a0002c0003t0004g0017 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4270-564T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15390646 | ||||||
| chr1:15390699
|
T | C | 1 | a0001c0002t0001g0079 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.4270-511T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15390699 | ||||||
| chr1:15390778
|
C | T | 3 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241 | 3 | HG02965.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.4270-432C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15390778 | ||||||
| chr1:15390857
|
T | C | 16 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(13): Show | 16 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.4270-353T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15390857 | ||||||
| chr1:15390871
|
G | A | 1 | a0004c0004t0004g0168 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.4270-339G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15390871 | ||||||
| chr1:15390936
|
A | G | 16 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(13): Show | 16 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.4270-274A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15390936 | ||||||
| chr1:15390957
|
A | C | 4 | a0001c0090t0048g0158a0003c0085t0055g0139a0040c0077t0037g0262others(1): Show | 4 | HG02258.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4270-253A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 32/33 | chr1 | 15390957 | ||||||
| chr1:15391302
|
G | GTTGTT | 4 | a0002c0003t0006g0157a0002c0003t0053g0176a0004c0057t0005g0189others(1): Show | 4 | HG02040.hp1 HG03130.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.4323+63_4323+67dup others(5): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15391302 | |||||
| chr1:15391342
|
A | G | 136 | a0002c0003t0003g0133a0002c0003t0003g0192a0002c0003t0004g0017others(133): Show | 136 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.4323+79A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15391342 | ||||||
| chr1:15391791
|
A | T | 1 | a0004c0087t0046g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4323+528A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15391791 | ||||||
| chr1:15391850
|
C | A | 6 | a0001c0002t0018g0156a0001c0002t0049g0101a0002c0019t0027g0244others(3): Show | 6 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.4323+587C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15391850 | ||||||
| chr1:15391870
|
T | G | 2 | a0004c0004t0004g0029a0004c0004t0004g0030 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.4323+607T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15391870 | ||||||
| chr1:15391974
|
T | G | 149 | a0001c0002t0018g0156a0001c0002t0049g0101a0002c0003t0003g0133others(146): Show | 149 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.4323+711T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15391974 | ||||||
| chr1:15392019
|
A | C | 1 | a0058c0106t0004g0042 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.4323+756A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15392019 | ||||||
| chr1:15392020
|
T | A | 1 | a0058c0106t0004g0042 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.4323+757T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15392020 | ||||||
| chr1:15392022
|
G | T | 1 | a0058c0106t0004g0042 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.4323+759G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15392022 | ||||||
| chr1:15392176
|
A | C | 2 | a0002c0003t0003g0133a0002c0007t0006g0108 | 2 | HG01952.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.4323+913A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15392176 | ||||||
| chr1:15392260
|
T | C | 4 | a0001c0001t0008g0160a0003c0056t0001g0107a0004c0004t0004g0168others(1): Show | 4 | HG00423.hp2 HG03490.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.4323+997T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15392260 | ||||||
| chr1:15392261
|
G | A | 1 | a0023c0130t0007g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4323+998G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15392261 | ||||||
| chr1:15392328
|
C | T | 4 | a0009c0011t0019g0144a0019c0022t0018g0015a0023c0127t0019g0184others(1): Show | 4 | HG02486.hp1 HG03471.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.4323+1065C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15392328 | ||||||
| chr1:15392343
|
T | C | 3 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241 | 3 | HG02965.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.4323+1080T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15392343 | ||||||
| chr1:15392360
|
G | A | 1 | a0002c0003t0004g0044 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.4323+1097G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15392360 | ||||||
| chr1:15392364
|
T | C | 5 | a0002c0003t0004g0044a0009c0011t0019g0144a0019c0022t0018g0015others(2): Show | 5 | HG01516.hp2 HG02486.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.4323+1101T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15392364 | ||||||
| chr1:15392393
|
A | G | 17 | a0002c0003t0003g0192a0002c0019t0004g0118a0002c0035t0006g0026others(14): Show | 17 | HG00738.hp1 HG01074.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.4323+1130A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15392393 | ||||||
| chr1:15392486
|
T | C | 5 | a0024c0027t0024g0258a0024c0027t0024g0288a0030c0115t0054g0203others(2): Show | 5 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.4323+1223T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15392486 | ||||||
| chr1:15392489
|
G | T | 1 | a0001c0001t0015g0267 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4323+1226G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15392489 | ||||||
| chr1:15392531
|
GA | G | 7 | a0001c0002t0018g0156a0001c0002t0049g0101a0002c0019t0027g0244others(4): Show | 7 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.4323+1280delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15392531 | |||||
| chr1:15392532
|
A | G | 40 | a0002c0003t0004g0017a0002c0003t0004g0044a0002c0003t0005g0135others(37): Show | 40 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.4323+1269A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15392532 | ||||||
| chr1:15392702
|
A | C | 1 | a0051c0100t0001g0091 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.4323+1439A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15392702 | ||||||
| chr1:15393068
|
A | T | 2 | a0002c0003t0006g0064a0006c0014t0003g0214 | 2 | HG02523.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.4323+1805A>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15393068 | ||||||
| chr1:15393072
|
C | CT | 29 | a0001c0001t0012g0128a0001c0002t0001g0061a0002c0018t0018g0153others(26): Show | 29 | HG00609.hp2 HG00735.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.4323+1829dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15393072 | |||||
| chr1:15393072
|
CT | C | 83 | a0001c0090t0048g0158a0002c0003t0003g0133a0002c0003t0004g0017others(80): Show | 83 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.4323+1829delT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15393072 | |||||
| chr1:15393072
|
CTT | C | 21 | a0002c0003t0014g0151a0002c0134t0003g0209a0004c0004t0007g0001others(18): Show | 21 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.4323+1828_4323+182 others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15393072 | |||||
| chr1:15393200
|
G | A | 3 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241 | 3 | HG02965.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.4323+1937G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15393200 | ||||||
| chr1:15393284
|
T | G | 15 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(12): Show | 15 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.4323+2021T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15393284 | ||||||
| chr1:15393420
|
A | G | 3 | a0018c0020t0022g0239a0018c0020t0022g0240a0018c0020t0022g0241 | 3 | HG02965.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.4323+2157A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15393420 | ||||||
| chr1:15393430
|
G | GCA | 12 | a0002c0019t0027g0244a0003c0055t0012g0213a0004c0004t0004g0067others(9): Show | 12 | HG00423.hp2 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.4323+2191_4323+219 others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15393430 | |||||
| chr1:15393430
|
G | GCACA | 70 | a0001c0002t0018g0156a0001c0002t0049g0101a0001c0013t0011g0266others(67): Show | 70 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.4323+2189_4323+219 others(8): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15393430 | |||||
| chr1:15393430
|
G | GCACACA | 30 | a0002c0003t0004g0017a0002c0003t0004g0044a0002c0003t0005g0135others(27): Show | 30 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.4323+2187_4323+219 others(10): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15393430 | |||||
| chr1:15393430
|
G | GCACACAC others(1): Show |
9 | a0002c0003t0005g0177a0002c0007t0005g0212a0004c0004t0004g0024others(6): Show | 9 | HG03688.hp2 NA18612.hp1 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.4323+2185_4323+219 others(12): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15393430 | |||||
| chr1:15393430
|
G | GCACACAC others(3): Show |
2 | a0004c0038t0014g0155a0004c0087t0046g0121 | 2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.4323+2183_4323+219 others(14): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15393430 | |||||
| chr1:15393430
|
G | GCACACAC others(5): Show |
8 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0038t0007g0143others(5): Show | 8 | HG01071.hp1 HG01106.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.4323+2181_4323+219 others(16): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15393430 | |||||
| chr1:15393430
|
G | GCACACAC others(7): Show |
2 | a0004c0004t0007g0002a0052c0088t0021g0242 | 2 | HG01070.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4323+2179_4323+219 others(18): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15393430 | |||||
| chr1:15393430
|
GCA | G | 16 | a0001c0002t0001g0079a0007c0012t0016g0187a0007c0012t0016g0256others(13): Show | 16 | HG01167.hp1 HG02280.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.4323+2191_4323+219 others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15393430 | |||||
| chr1:15393457
|
G | A | 2 | a0032c0120t0034g0259a0059c0104t0045g0014 | 2 | HG02559.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4323+2194G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15393457 | ||||||
| chr1:15393485
|
G | GA | 3 | a0007c0059t0014g0167a0007c0101t0014g0119a0057c0105t0004g0059 | 3 | HG00735.hp2 HG00738.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.4323+2228dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15393485 | |||||
| chr1:15393514
|
G | A | 4 | a0001c0001t0013g0104a0001c0102t0012g0146a0005c0005t0015g0286others(1): Show | 4 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.4323+2251G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15393514 | ||||||
| chr1:15393607
|
C | CT | 16 | a0001c0001t0002g0081a0001c0002t0018g0156a0001c0002t0049g0101others(13): Show | 16 | HG02145.hp1 HG02145.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.4323+2356dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15393607 | |||||
| chr1:15393608
|
T | C | 1 | a0001c0001t0012g0161 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4323+2345T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15393608 | ||||||
| chr1:15393757
|
T | C | 153 | a0001c0002t0018g0156a0001c0002t0049g0101a0001c0013t0011g0266others(150): Show | 153 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.4323+2494T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15393757 | ||||||
| chr1:15393762
|
CT | C | 6 | a0003c0006t0002g0103a0003c0006t0002g0122a0003c0006t0008g0171others(3): Show | 6 | HG00609.hp2 HG02523.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.4323+2500delT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15393762 | ||||||
| chr1:15393798
|
A | G | 1 | a0014c0110t0008g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4323+2535A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15393798 | ||||||
| chr1:15393922
|
G | A | 2 | a0019c0022t0004g0022a0019c0022t0004g0071 | 2 | NA18992.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.4323+2659G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15393922 | ||||||
| chr1:15394243
|
T | C | 1 | a0004c0087t0046g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4323+2980T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15394243 | ||||||
| chr1:15394258
|
G | C | 4 | a0001c0032t0014g0152a0001c0032t0023g0282a0016c0040t0021g0249others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.4323+2995G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15394258 | ||||||
| chr1:15394389
|
G | C | 1 | a0024c0027t0024g0288 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4324-2908G>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15394389 | ||||||
| chr1:15394400
|
T | G | 1 | a0001c0102t0012g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4324-2897T>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15394400 | ||||||
| chr1:15394403
|
A | C | 40 | a0002c0003t0004g0017a0002c0003t0004g0044a0002c0003t0005g0135others(37): Show | 40 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.4324-2894A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15394403 | ||||||
| chr1:15394462
|
C | T | 7 | a0001c0002t0001g0023a0001c0002t0001g0061a0001c0002t0001g0065others(4): Show | 7 | HG02135.hp2 HG02165.hp2 NA18986.hp1 others(4): Show |
intron_variant | MODIFIER | c.4324-2835C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15394462 | ||||||
| chr1:15394496
|
A | G | 1 | a0004c0087t0046g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4324-2801A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15394496 | ||||||
| chr1:15394556
|
G | A | 1 | a0002c0003t0005g0135 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4324-2741G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15394556 | ||||||
| chr1:15394809
|
G | T | 1 | a0002c0018t0018g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4324-2488G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15394809 | ||||||
| chr1:15394883
|
G | T | 7 | a0002c0018t0018g0153a0002c0080t0019g0181a0009c0011t0019g0144others(4): Show | 7 | HG02486.hp1 HG02896.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.4324-2414G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15394883 | ||||||
| chr1:15394979
|
G | A | 1 | a0007c0033t0014g0068 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4324-2318G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15394979 | ||||||
| chr1:15395008
|
A | G | 22 | a0002c0018t0007g0140a0002c0018t0021g0247a0003c0098t0029g0237others(19): Show | 22 | HG00735.hp2 HG00738.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.4324-2289A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15395008 | ||||||
| chr1:15395183
|
G | A | 1 | a0012c0051t0011g0284 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4324-2114G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15395183 | ||||||
| chr1:15395286
|
C | T | 95 | a0001c0013t0011g0266a0002c0003t0003g0133a0002c0003t0003g0192others(92): Show | 95 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.4324-2011C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15395286 | ||||||
| chr1:15395307
|
C | CA | 145 | a0001c0002t0001g0076a0001c0002t0044g0169a0001c0008t0008g0204others(142): Show | 145 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.4324-1973dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15395307 | |||||
| chr1:15395307
|
C | CAA | 17 | a0001c0002t0018g0156a0001c0002t0049g0101a0001c0090t0048g0158others(14): Show | 17 | HG02056.hp1 HG02145.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.4324-1974_4324-197 others(6): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15395307 | |||||
| chr1:15395330
|
G | A | 1 | a0005c0005t0015g0275 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4324-1967G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15395330 | ||||||
| chr1:15395363
|
C | G | 5 | a0024c0027t0024g0258a0024c0027t0024g0288a0030c0115t0054g0203others(2): Show | 5 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.4324-1934C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15395363 | ||||||
| chr1:15395441
|
C | A | 4 | a0001c0090t0048g0158a0003c0085t0055g0139a0040c0077t0037g0262others(1): Show | 4 | HG02258.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4324-1856C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15395441 | ||||||
| chr1:15395590
|
C | A | 3 | a0002c0018t0018g0153a0002c0080t0019g0181a0039c0126t0019g0185 | 3 | HG02896.hp1 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4324-1707C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15395590 | ||||||
| chr1:15395634
|
G | T | 11 | a0009c0011t0019g0144a0018c0020t0022g0239a0018c0020t0022g0240others(8): Show | 11 | HG01167.hp1 HG02486.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.4324-1663G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15395634 | ||||||
| chr1:15395730
|
A | G | 12 | a0001c0002t0018g0156a0001c0002t0049g0101a0001c0090t0048g0158others(9): Show | 12 | HG02145.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.4324-1567A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15395730 | ||||||
| chr1:15395765
|
T | C | 4 | a0029c0114t0056g0199a0032c0120t0034g0259a0047c0089t0050g0105others(1): Show | 4 | HG01167.hp1 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4324-1532T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15395765 | ||||||
| chr1:15395796
|
A | AT | 33 | a0002c0003t0014g0151a0002c0018t0007g0140a0002c0018t0021g0247others(30): Show | 33 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.4324-1491dupT | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15395796 | |||||
| chr1:15396025
|
A | G | 6 | a0002c0003t0005g0177a0002c0007t0005g0212a0004c0004t0004g0024others(3): Show | 6 | NA18612.hp1 NA18970.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.4324-1272A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396025 | ||||||
| chr1:15396047
|
C | T | 10 | a0004c0087t0046g0121a0007c0012t0016g0187a0007c0012t0016g0256others(7): Show | 10 | HG02572.hp1 HG02615.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.4324-1250C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396047 | ||||||
| chr1:15396048
|
A | G | 154 | a0001c0002t0018g0156a0001c0002t0049g0101a0001c0013t0011g0266others(151): Show | 154 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.4324-1249A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396048 | ||||||
| chr1:15396077
|
A | C | 1 | a0009c0028t0011g0290 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.4324-1220A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396077 | ||||||
| chr1:15396078
|
G | A | 1 | a0004c0087t0046g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4324-1219G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396078 | ||||||
| chr1:15396255
|
G | A | 72 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(69): Show | 72 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.4324-1042G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396255 | ||||||
| chr1:15396260
|
T | C | 5 | a0001c0002t0018g0156a0001c0002t0049g0101a0002c0019t0027g0244others(2): Show | 5 | HG02145.hp2 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.4324-1037T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396260 | ||||||
| chr1:15396344
|
A | C | 2 | a0023c0127t0019g0184a0041c0076t0038g0289 | 2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4324-953A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396344 | ||||||
| chr1:15396506
|
G | A | 2 | a0032c0120t0034g0259a0059c0104t0045g0014 | 2 | HG02559.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4324-791G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396506 | ||||||
| chr1:15396574
|
C | A | 1 | a0004c0004t0004g0067 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.4324-723C>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396574 | ||||||
| chr1:15396627
|
G | A | 10 | a0002c0018t0018g0153a0002c0080t0019g0181a0009c0011t0019g0144others(7): Show | 10 | HG01167.hp1 HG02486.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.4324-670G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396627 | ||||||
| chr1:15396797
|
A | C | 1 | a0003c0009t0001g0035 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4324-500A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396797 | ||||||
| chr1:15396799
|
G | A | 1 | a0003c0009t0001g0035 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4324-498G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396799 | ||||||
| chr1:15396804
|
T | A | 1 | a0003c0009t0001g0035 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4324-493T>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396804 | ||||||
| chr1:15396807
|
C | T | 9 | a0001c0002t0018g0156a0001c0002t0049g0101a0001c0090t0048g0158others(6): Show | 9 | HG02145.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.4324-490C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396807 | ||||||
| chr1:15396809
|
C | G | 1 | a0001c0001t0008g0149 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4324-488C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396809 | ||||||
| chr1:15396828
|
G | T | 1 | a0003c0009t0001g0035 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4324-469G>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396828 | ||||||
| chr1:15396886
|
T | C | 94 | a0001c0013t0011g0266a0002c0003t0003g0133a0002c0003t0003g0192others(91): Show | 94 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.4324-411T>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396886 | ||||||
| chr1:15396912
|
C | T | 11 | a0002c0003t0014g0151a0004c0004t0007g0001a0004c0004t0007g0002others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.4324-385C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396912 | ||||||
| chr1:15396955
|
C | T | 1 | a0002c0003t0006g0157 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4324-342C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396955 | ||||||
| chr1:15396981
|
A | G | 4 | a0001c0090t0048g0158a0003c0085t0055g0139a0040c0077t0037g0262others(1): Show | 4 | HG02258.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4324-316A>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15396981 | ||||||
| chr1:15397011
|
C | T | 2 | a0001c0008t0012g0205a0005c0005t0015g0268 | 2 | HG03688.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.4324-286C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15397011 | ||||||
| chr1:15397020
|
T | TA | 48 | a0001c0002t0001g0079a0001c0002t0001g0188a0001c0013t0011g0266others(45): Show | 48 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.4324-256dupA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15397020 | |||||
| chr1:15397020
|
T | TAAAAAAA others(6): Show |
4 | a0001c0090t0048g0158a0003c0085t0055g0139a0040c0077t0037g0262others(1): Show | 4 | HG02258.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4324-268_4324-256d others(15): Show |
FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15397020 | |||||
| chr1:15397020
|
TA | T | 116 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0049others(113): Show | 116 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.4324-256delA | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | INFO_REALIGN_3_PRIME | chr1 | 15397020 | |||||
| chr1:15397051
|
C | T | 14 | a0001c0002t0018g0156a0001c0002t0049g0101a0002c0019t0027g0244others(11): Show | 14 | HG01167.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.4324-246C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15397051 | ||||||
| chr1:15397060
|
G | A | 2 | a0002c0035t0006g0026a0012c0097t0003g0141 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4324-237G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15397060 | ||||||
| chr1:15397064
|
G | A | 4 | a0001c0090t0048g0158a0003c0085t0055g0139a0040c0077t0037g0262others(1): Show | 4 | HG02258.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4324-233G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15397064 | ||||||
| chr1:15397084
|
G | A | 2 | a0006c0014t0005g0255a0057c0105t0004g0059 | 2 | HG00642.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.4324-213G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15397084 | ||||||
| chr1:15397130
|
G | A | 4 | a0001c0090t0048g0158a0003c0085t0055g0139a0040c0077t0037g0262others(1): Show | 4 | HG02258.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4324-167G>A | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15397130 | ||||||
| chr1:15397164
|
C | G | 1 | a0001c0092t0002g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4324-133C>G | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15397164 | ||||||
| chr1:15397185
|
C | T | 1 | a0004c0087t0046g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4324-112C>T | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15397185 | ||||||
| chr1:15397225
|
A | C | 2 | a0006c0014t0005g0255a0057c0105t0004g0059 | 2 | HG00642.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.4324-72A>C | FHAD1 | ENSG00000142621.21 | transcript | ENST00000688493.1 | protein_coding | 33/33 | chr1 | 15397225 |