Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 81533 |
|---|---|
| ensemblid | ENSG00000129636.13 |
| hgncid | 30697 |
| symbol | ITFG1 |
| name | integrin alpha FG-GAP repeat containing 1 |
| refseq_nuc | NM_030790.5 |
| refseq_prot | NP_110417.2 |
| ensembl_nuc | ENST00000320640.11 |
| ensembl_prot | ENSP00000319918.6 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 47154391 |
| end | 47461063 |
| strand | - |
| ver | v1.2 |
| region | chr16:47154391-47461063 |
| region5000 | chr16:47149391-47466063 |
| regionname0 | ITFG1_chr16_47154391_47461063 |
| regionname5000 | ITFG1_chr16_47149391_47466063 |
| 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 | 612 | 110 | 70 | 20 | 4 | 4 | 10 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1839 | 81 | 48 | 13 | 4 | 4 | 10 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| c0002 | 0/0 | 1839 | 26 | 20 | 6 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| c0003 | 0/0 | 1839 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| c0004 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| c0005 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1347 | 82 | 47 | 15 | 4 | 4 | 10 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| t0002 | 0/0 | 1347 | 18 | 13 | 5 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| t0003 | 0/0 | 1347 | 7 | 7 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| t0004 | 0/0 | 1344 | 3 | 3 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| 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 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0018 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0025 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1839 | 81 | 48 | 13 | 4 | 4 | 10 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| a0001c0002 | 0/0 | 1839 | 26 | 20 | 6 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| a0001c0003 | 0/0 | 1839 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| a0001c0004 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| a0001c0005 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3185 | 74 | 41 | 13 | 4 | 4 | 10 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| a0001c0001t0003 | 0/0 | 3185 | 7 | 7 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| a0001c0002t0001 | 0/0 | 3185 | 5 | 4 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| a0001c0002t0002 | 0/0 | 3185 | 18 | 13 | 5 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| a0001c0002t0004 | 0/0 | 3182 | 3 | 3 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| a0001c0003t0001 | 0/0 | 3185 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| a0001c0004t0001 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| a0001c0005t0001 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | copy fasta | chr16 | 47149391 | 47466063 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0018 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0025 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0002t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0003t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| a0001c0005t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | GBR | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | FIN | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0088 | AMR | PUR | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0087 | AMR | PUR | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0078 | AMR | PUR | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0086 | AMR | CLM | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0077 | AMR | CLM | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | CLM | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | ACB | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0075 | AFR | ACB | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | ACB | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0083 | AFR | ACB | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0093 | AFR | ACB | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02622 | hp1 | a0001 | c0004 | t0001 | g0071 | AFR | GWD | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0081 | AFR | GWD | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0090 | AFR | GWD | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0096 | AFR | GWD | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0073 | AFR | GWD | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02895 | hp2 | a0001 | c0002 | t0004 | g0064 | AFR | GWD | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02897 | hp1 | a0001 | c0002 | t0004 | g0065 | AFR | GWD | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | ESN | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0080 | AFR | ESN | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | GWD | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03098 | hp1 | a0001 | c0002 | t0004 | g0095 | AFR | MSL | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0079 | AFR | ESN | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0089 | AFR | MSL | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0082 | AFR | GWD | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | YRI | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0076 | AFR | YRI | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0084 | AFR | LWK | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | LWK | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | YRI | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0085 | AFR | YRI | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | ASW | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ASW | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02109 | hp2 | a0001 | c0005 | t0001 | g0103 | AFR | ACB | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | ACB | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0074 | AFR | MSL | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | USA | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0072 | AFR | USA | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | LWK | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | LWK | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0018 | REF | REF | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0025 | REF | REF | ITFG1_chr16_47149391_47466063 | ITFG1 | chr16 | 47149391 | 47466063 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:47237965
|
T | C | 2 | a0001c0002a0001c0004 | 27 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(24): Show |
splice_region_variant&synonymous_variant | LOW | c.1374A>G | p.Thr458Thr | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/18 | 1392/3185 | 1374/1839 | 458/612 | chr16 | 47237965 | ||
| chr16:47260548
|
T | C | 1 | a0001c0004 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1218A>G | p.Glu406Glu | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 11/18 | 1236/3185 | 1218/1839 | 406/612 | chr16 | 47260548 | ||
| chr16:47451404
|
T | C | 1 | a0001c0005 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.552A>G | p.Leu184Leu | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/18 | 570/3185 | 552/1839 | 184/612 | chr16 | 47451404 | ||
| chr16:47461001
|
C | T | 1 | a0001c0003 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.45G>A | p.Ser15Ser | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 1/18 | 63/3185 | 45/1839 | 15/612 | chr16 | 47461001 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:47154400
|
G | T | 2 | a0001c0002t0002a0001c0002t0004 | 21 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1319C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 18/18 | 1319 | chr16 | 47154400 | |||||
| chr16:47154488
|
GAAC | G | 1 | a0001c0002t0004 | 3 | HG02895.hp2 HG02897.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1228_*1230delGTT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 18/18 | 1228 | chr16 | 47154488 | |||||
| chr16:47155153
|
G | C | 1 | a0001c0001t0003 | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*566C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 18/18 | 566 | chr16 | 47155153 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:47156085
|
A | G | 1 | a0001c0002t0002g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1780-307T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 17/17 | chr16 | 47156085 | ||||||
| chr16:47156106
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1780-328G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 17/17 | chr16 | 47156106 | ||||||
| chr16:47156226
|
G | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(17): Show | 20 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.1780-448C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 17/17 | chr16 | 47156226 | ||||||
| chr16:47156265
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1780-487G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 17/17 | chr16 | 47156265 | ||||||
| chr16:47156685
|
G | C | 19 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(16): Show | 19 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.1780-907C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 17/17 | chr16 | 47156685 | ||||||
| chr16:47157590
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1779+1283T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 17/17 | chr16 | 47157590 | ||||||
| chr16:47157735
|
T | C | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1779+1138A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 17/17 | chr16 | 47157735 | ||||||
| chr16:47158518
|
A | G | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1779+355T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 17/17 | chr16 | 47158518 | ||||||
| chr16:47158525
|
A | G | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1779+348T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 17/17 | chr16 | 47158525 | ||||||
| chr16:47158846
|
A | G | 41 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1779+27T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 17/17 | chr16 | 47158846 | ||||||
| chr16:47159935
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1662-945A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 16/17 | chr16 | 47159935 | ||||||
| chr16:47159991
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1662-1001G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 16/17 | chr16 | 47159991 | ||||||
| chr16:47160081
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1662-1091G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 16/17 | chr16 | 47160081 | ||||||
| chr16:47160140
|
T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0043 | 2 | HG01258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1662-1150A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 16/17 | chr16 | 47160140 | ||||||
| chr16:47160609
|
A | G | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1661+1141T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 16/17 | chr16 | 47160609 | ||||||
| chr16:47160820
|
T | G | 3 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0039 | 3 | HG00140.hp2 HG00280.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1661+930A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 16/17 | chr16 | 47160820 | ||||||
| chr16:47160897
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1661+853G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 16/17 | chr16 | 47160897 | ||||||
| chr16:47161085
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1661+665G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 16/17 | chr16 | 47161085 | ||||||
| chr16:47161392
|
A | G | 5 | a0001c0001t0001g0031a0001c0001t0001g0057a0001c0001t0001g0061others(2): Show | 5 | HG00642.hp2 HG02735.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1661+358T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 16/17 | chr16 | 47161392 | ||||||
| chr16:47162086
|
C | T | 43 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(40): Show | 43 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.1579-254G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 15/17 | chr16 | 47162086 | ||||||
| chr16:47163275
|
A | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0042 | 2 | HG02896.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1454-611T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47163275 | ||||||
| chr16:47163582
|
A | G | 20 | a0001c0002t0001g0094a0001c0002t0002g0072a0001c0002t0002g0073others(17): Show | 20 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1454-918T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47163582 | ||||||
| chr16:47163914
|
TAC | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(46): Show | 49 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.1454-1252_1454-125 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47163914 | ||||||
| chr16:47163914
|
TACAC | T | 9 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0042others(6): Show | 9 | HG00642.hp2 HG01258.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1454-1254_1454-125 others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47163914 | ||||||
| chr16:47163914
|
TACACAC | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0066 | 3 | HG01074.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1454-1256_1454-125 others(10): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47163914 | ||||||
| chr16:47163934
|
C | T | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1454-1270G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47163934 | ||||||
| chr16:47163944
|
C | T | 2 | a0001c0001t0003g0068a0001c0004t0001g0071 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1454-1280G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47163944 | ||||||
| chr16:47163948
|
C | T | 25 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0091others(22): Show | 25 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1454-1284G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47163948 | ||||||
| chr16:47163950
|
C | T | 7 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(4): Show | 7 | HG01361.hp1 HG01496.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1454-1286G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47163950 | ||||||
| chr16:47163950
|
CACAT | C | 6 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0091others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1454-1290_1454-128 others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47163950 | ||||||
| chr16:47163952
|
CAT | C | 23 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(20): Show | 23 | HG01109.hp2 HG01891.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1454-1290_1454-128 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47163952 | ||||||
| chr16:47163954
|
T | C | 3 | a0001c0002t0001g0067a0001c0002t0001g0096a0001c0002t0002g0077 | 3 | HG01361.hp1 HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1454-1290A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47163954 | ||||||
| chr16:47163954
|
T | TAC | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-1292_1454-129 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47163954 | ||||||
| chr16:47163954
|
T | TACAC | 3 | a0001c0002t0002g0086a0001c0002t0002g0087a0001c0002t0002g0088 | 3 | HG00735.hp2 HG01074.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1454-1294_1454-129 others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47163954 | ||||||
| chr16:47164060
|
T | G | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1454-1396A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47164060 | ||||||
| chr16:47164126
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1454-1462G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47164126 | ||||||
| chr16:47164519
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1454-1855A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47164519 | ||||||
| chr16:47164632
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1454-1968C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47164632 | ||||||
| chr16:47164762
|
A | C | 1 | a0001c0001t0001g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1454-2098T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47164762 | ||||||
| chr16:47164847
|
C | G | 1 | a0001c0001t0001g0022 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1454-2183G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47164847 | ||||||
| chr16:47165101
|
A | T | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1454-2437T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47165101 | ||||||
| chr16:47165670
|
G | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-3006C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47165670 | ||||||
| chr16:47166254
|
A | G | 27 | a0001c0002t0001g0067a0001c0002t0001g0079a0001c0002t0001g0080others(24): Show | 27 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1454-3590T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47166254 | ||||||
| chr16:47166595
|
G | A | 1 | a0001c0002t0002g0077 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1454-3931C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47166595 | ||||||
| chr16:47166763
|
G | GTGAACAT others(1): Show |
109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1454-4100_1454-409 others(12): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47166763 | ||||||
| chr16:47166765
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1454-4101A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47166765 | ||||||
| chr16:47166768
|
C | CAA | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1454-4105_1454-410 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47166768 | ||||||
| chr16:47166770
|
C | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1454-4106G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47166770 | ||||||
| chr16:47166772
|
C | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1454-4108G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47166772 | ||||||
| chr16:47166774
|
A | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1454-4110T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47166774 | ||||||
| chr16:47166778
|
A | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1454-4114T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47166778 | ||||||
| chr16:47166896
|
C | G | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1454-4232G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47166896 | ||||||
| chr16:47167047
|
C | G | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1454-4383G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47167047 | ||||||
| chr16:47167544
|
C | T | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1454-4880G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47167544 | ||||||
| chr16:47167610
|
G | T | 40 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(37): Show | 40 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.1454-4946C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47167610 | ||||||
| chr16:47167620
|
C | T | 24 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0002g0072others(21): Show | 24 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1454-4956G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47167620 | ||||||
| chr16:47168315
|
A | G | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1454-5651T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47168315 | ||||||
| chr16:47168545
|
G | GT | 19 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0030others(16): Show | 19 | HG01361.hp1 HG01361.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1454-5882dupA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47168545 | ||||||
| chr16:47169003
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1454-6339A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47169003 | ||||||
| chr16:47170386
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1454-7722T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47170386 | ||||||
| chr16:47170517
|
C | G | 1 | a0001c0002t0001g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1454-7853G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47170517 | ||||||
| chr16:47170675
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1454-8011C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47170675 | ||||||
| chr16:47170736
|
C | CT | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(78): Show | 81 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1454-8073dupA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47170736 | ||||||
| chr16:47170736
|
C | CTT | 24 | a0001c0001t0001g0005a0001c0002t0001g0067a0001c0002t0001g0079others(21): Show | 24 | HG00735.hp2 HG01109.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.1454-8074_1454-807 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47170736 | ||||||
| chr16:47170830
|
G | A | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1454-8166C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47170830 | ||||||
| chr16:47171025
|
G | A | 1 | a0001c0004t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1454-8361C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47171025 | ||||||
| chr16:47171029
|
C | CT | 5 | a0001c0002t0001g0067a0001c0002t0002g0078a0001c0002t0002g0086others(2): Show | 5 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1454-8366dupA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47171029 | ||||||
| chr16:47171029
|
CT | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(63): Show | 66 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.1454-8366delA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47171029 | ||||||
| chr16:47171254
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1454-8590A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47171254 | ||||||
| chr16:47171255
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0110 | 2 | HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1454-8591C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47171255 | ||||||
| chr16:47171717
|
TTTTG | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0050 | 2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1454-9057_1454-905 others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47171717 | ||||||
| chr16:47171849
|
T | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1454-9185A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47171849 | ||||||
| chr16:47173195
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1454-10531G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47173195 | ||||||
| chr16:47175117
|
A | G | 4 | a0001c0002t0001g0094a0001c0002t0002g0082a0001c0002t0002g0083others(1): Show | 4 | HG02257.hp2 HG02922.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1454-12453T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47175117 | ||||||
| chr16:47175794
|
T | C | 1 | a0001c0002t0002g0083 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1454-13130A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47175794 | ||||||
| chr16:47176029
|
C | G | 2 | a0001c0002t0002g0075a0001c0002t0002g0076 | 2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1454-13365G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47176029 | ||||||
| chr16:47176057
|
G | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1454-13393C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47176057 | ||||||
| chr16:47176268
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1454-13604A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47176268 | ||||||
| chr16:47176362
|
C | A | 1 | a0001c0001t0001g0034 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1454-13698G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47176362 | ||||||
| chr16:47176941
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1454-14277G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47176941 | ||||||
| chr16:47176953
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-14289G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47176953 | ||||||
| chr16:47176953
|
CT | C | 7 | a0001c0001t0001g0038a0001c0001t0001g0102a0001c0001t0001g0107others(4): Show | 7 | HG01074.hp2 HG01169.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.1454-14290delA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47176953 | ||||||
| chr16:47176956
|
T | C | 6 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 6 | HG02559.hp1 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1454-14292A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47176956 | ||||||
| chr16:47176957
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1454-14293A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47176957 | ||||||
| chr16:47177145
|
A | T | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1454-14481T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47177145 | ||||||
| chr16:47177311
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1454-14647G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47177311 | ||||||
| chr16:47177321
|
T | C | 37 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(34): Show | 37 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1454-14657A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47177321 | ||||||
| chr16:47177573
|
A | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1454-14909T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47177573 | ||||||
| chr16:47177691
|
T | C | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG00735.hp1 HG01169.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1454-15027A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47177691 | ||||||
| chr16:47178186
|
T | A | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1454-15522A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47178186 | ||||||
| chr16:47179077
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1454-16413T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47179077 | ||||||
| chr16:47179639
|
T | TA | 40 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(37): Show | 40 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.1454-16976dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47179639 | ||||||
| chr16:47179702
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-17038G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47179702 | ||||||
| chr16:47179880
|
C | T | 2 | a0001c0002t0001g0094a0001c0005t0001g0103 | 2 | HG02109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1454-17216G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47179880 | ||||||
| chr16:47180198
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1454-17534C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180198 | ||||||
| chr16:47180298
|
T | TG | 41 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1454-17635dupC | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180298 | ||||||
| chr16:47180379
|
C | T | 2 | a0001c0002t0001g0079a0001c0002t0001g0080 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1454-17715G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180379 | ||||||
| chr16:47180386
|
C | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0054 | 2 | HG00609.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1454-17722G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180386 | ||||||
| chr16:47180436
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-17772T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180436 | ||||||
| chr16:47180447
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-17783C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180447 | ||||||
| chr16:47180461
|
T | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0026 | 2 | HG00140.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1454-17797A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180461 | ||||||
| chr16:47180475
|
T | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-17811A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180475 | ||||||
| chr16:47180506
|
C | T | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-17842G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180506 | ||||||
| chr16:47180507
|
T | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-17843A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180507 | ||||||
| chr16:47180528
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-17864T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180528 | ||||||
| chr16:47180549
|
T | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-17885A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180549 | ||||||
| chr16:47180573
|
T | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-17909A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180573 | ||||||
| chr16:47180594
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-17930T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180594 | ||||||
| chr16:47180616
|
C | T | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-17952G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180616 | ||||||
| chr16:47180618
|
T | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-17954A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180618 | ||||||
| chr16:47180672
|
C | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-18008G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180672 | ||||||
| chr16:47180692
|
G | T | 1 | a0001c0001t0001g0039 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1454-18028C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180692 | ||||||
| chr16:47180693
|
T | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-18029A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180693 | ||||||
| chr16:47180705
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-18041C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180705 | ||||||
| chr16:47180716
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-18052T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180716 | ||||||
| chr16:47180724
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-18060T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180724 | ||||||
| chr16:47180752
|
G | A | 27 | a0001c0002t0001g0067a0001c0002t0001g0079a0001c0002t0001g0080others(24): Show | 27 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1454-18088C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180752 | ||||||
| chr16:47180764
|
G | C | 41 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1454-18100C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180764 | ||||||
| chr16:47180795
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1454-18131G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47180795 | ||||||
| chr16:47181018
|
G | A | 1 | a0001c0004t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1454-18354C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181018 | ||||||
| chr16:47181053
|
C | T | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1454-18389G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181053 | ||||||
| chr16:47181054
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1454-18390C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181054 | ||||||
| chr16:47181058
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1454-18394C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181058 | ||||||
| chr16:47181107
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1454-18443G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181107 | ||||||
| chr16:47181173
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1454-18509G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181173 | ||||||
| chr16:47181183
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1454-18519G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181183 | ||||||
| chr16:47181189
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1454-18525G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181189 | ||||||
| chr16:47181232
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1454-18568G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181232 | ||||||
| chr16:47181272
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1454-18608G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181272 | ||||||
| chr16:47181272
|
CGTCTGGG others(17): Show |
C | 3 | a0001c0002t0002g0072a0001c0002t0002g0078a0001c0002t0002g0081 | 3 | HG01109.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1454-18632_1454-18 others(30): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181272 | ||||||
| chr16:47181290
|
C | G | 1 | a0001c0001t0001g0007 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1454-18626G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181290 | ||||||
| chr16:47181362
|
GCCCCCCG others(43): Show |
G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-18748_1454-18 others(56): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181362 | ||||||
| chr16:47181385
|
C | T | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1454-18721G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181385 | ||||||
| chr16:47181399
|
A | G | 38 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(35): Show | 38 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1454-18735T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181399 | ||||||
| chr16:47181422
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-18758G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181422 | ||||||
| chr16:47181423
|
G | A | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1454-18759C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181423 | ||||||
| chr16:47181450
|
T | TG | 26 | a0001c0002t0001g0067a0001c0002t0001g0079a0001c0002t0001g0080others(23): Show | 26 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1454-18787dupC | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181450 | ||||||
| chr16:47181469
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1454-18805G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181469 | ||||||
| chr16:47181523
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1454-18859G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181523 | ||||||
| chr16:47181540
|
T | C | 41 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1454-18876A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181540 | ||||||
| chr16:47181551
|
TG | T | 41 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1454-18888delC | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181551 | ||||||
| chr16:47181571
|
C | T | 2 | a0001c0002t0002g0073a0001c0002t0002g0074 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1454-18907G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181571 | ||||||
| chr16:47181620
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG00735.hp1 HG01169.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1454-18956G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181620 | ||||||
| chr16:47181625
|
G | A | 2 | a0001c0002t0004g0064a0001c0002t0004g0065 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1454-18961C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181625 | ||||||
| chr16:47181677
|
A | T | 1 | a0001c0001t0001g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1454-19013T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181677 | ||||||
| chr16:47181885
|
C | G | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1454-19221G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181885 | ||||||
| chr16:47181980
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1454-19316C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47181980 | ||||||
| chr16:47182045
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG01361.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1454-19381C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47182045 | ||||||
| chr16:47182386
|
C | CA | 41 | a0001c0001t0001g0006a0001c0001t0001g0100a0001c0001t0001g0101others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1454-19723dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47182386 | ||||||
| chr16:47182653
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1454-19989T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47182653 | ||||||
| chr16:47182694
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1454-20030C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47182694 | ||||||
| chr16:47182776
|
C | T | 34 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(31): Show | 34 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1454-20112G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47182776 | ||||||
| chr16:47182806
|
C | A | 1 | a0001c0002t0001g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1454-20142G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47182806 | ||||||
| chr16:47182922
|
C | T | 34 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(31): Show | 34 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1454-20258G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47182922 | ||||||
| chr16:47182926
|
C | T | 1 | a0001c0002t0001g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1454-20262G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47182926 | ||||||
| chr16:47183438
|
C | T | 5 | a0001c0001t0001g0031a0001c0001t0001g0057a0001c0001t0001g0061others(2): Show | 5 | HG00642.hp2 HG02735.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1454-20774G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47183438 | ||||||
| chr16:47183494
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1454-20830C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47183494 | ||||||
| chr16:47183557
|
C | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0051 | 2 | HG00741.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1454-20893G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47183557 | ||||||
| chr16:47184085
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1454-21421T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47184085 | ||||||
| chr16:47184086
|
T | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0023 | 2 | HG00140.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1454-21422A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47184086 | ||||||
| chr16:47184148
|
G | C | 41 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1454-21484C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47184148 | ||||||
| chr16:47184150
|
G | C | 10 | a0001c0002t0002g0072a0001c0002t0002g0075a0001c0002t0002g0076others(7): Show | 10 | HG01109.hp2 HG01891.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1454-21486C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47184150 | ||||||
| chr16:47184281
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1454-21617G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47184281 | ||||||
| chr16:47184562
|
C | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0100a0001c0001t0001g0101others(1): Show | 4 | HG02896.hp2 HG02970.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1454-21898G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47184562 | ||||||
| chr16:47184630
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1454-21966C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47184630 | ||||||
| chr16:47184695
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1454-22031G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47184695 | ||||||
| chr16:47184982
|
G | C | 1 | a0001c0001t0001g0049 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1454-22318C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47184982 | ||||||
| chr16:47184993
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0042 | 2 | HG02896.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1454-22329T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47184993 | ||||||
| chr16:47185251
|
T | C | 1 | a0001c0002t0002g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1454-22587A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47185251 | ||||||
| chr16:47185305
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1454-22641G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47185305 | ||||||
| chr16:47185422
|
A | C | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1454-22758T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47185422 | ||||||
| chr16:47185470
|
C | T | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1454-22806G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47185470 | ||||||
| chr16:47185524
|
T | C | 1 | a0001c0002t0002g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1454-22860A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47185524 | ||||||
| chr16:47185830
|
C | T | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1454-23166G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47185830 | ||||||
| chr16:47185841
|
A | C | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1454-23177T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47185841 | ||||||
| chr16:47186281
|
G | A | 41 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1454-23617C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47186281 | ||||||
| chr16:47186348
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0050 | 2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1454-23684C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47186348 | ||||||
| chr16:47186829
|
T | C | 1 | a0001c0002t0002g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1454-24165A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47186829 | ||||||
| chr16:47186891
|
C | G | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1454-24227G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47186891 | ||||||
| chr16:47186964
|
G | A | 4 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0091others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454-24300C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47186964 | ||||||
| chr16:47186965
|
T | A | 4 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0091others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454-24301A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47186965 | ||||||
| chr16:47186983
|
C | T | 4 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0091others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454-24319G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47186983 | ||||||
| chr16:47187013
|
T | G | 4 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0091others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454-24349A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47187013 | ||||||
| chr16:47187138
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1454-24474G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47187138 | ||||||
| chr16:47187362
|
T | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG01496.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1454-24698A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47187362 | ||||||
| chr16:47187456
|
C | T | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1454-24792G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47187456 | ||||||
| chr16:47187533
|
T | C | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1454-24869A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47187533 | ||||||
| chr16:47187693
|
T | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1454-25029A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47187693 | ||||||
| chr16:47187713
|
C | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1454-25049G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47187713 | ||||||
| chr16:47187743
|
A | C | 3 | a0001c0002t0002g0086a0001c0002t0002g0087a0001c0002t0002g0088 | 3 | HG00735.hp2 HG01074.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1454-25079T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47187743 | ||||||
| chr16:47188058
|
G | A | 27 | a0001c0002t0001g0067a0001c0002t0001g0079a0001c0002t0001g0080others(24): Show | 27 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1454-25394C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47188058 | ||||||
| chr16:47188277
|
G | T | 1 | a0001c0001t0001g0020 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1454-25613C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47188277 | ||||||
| chr16:47188340
|
A | G | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1454-25676T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47188340 | ||||||
| chr16:47188528
|
C | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG00735.hp1 HG01169.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1454-25864G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47188528 | ||||||
| chr16:47188555
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1454-25891A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47188555 | ||||||
| chr16:47188625
|
A | AG | 12 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0030others(9): Show | 12 | HG01109.hp1 HG01109.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1454-25962dupC | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47188625 | ||||||
| chr16:47188773
|
G | GA | 36 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(33): Show | 36 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1454-26110dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47188773 | ||||||
| chr16:47188847
|
C | T | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1454-26183G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47188847 | ||||||
| chr16:47189381
|
A | T | 3 | a0001c0002t0002g0072a0001c0002t0002g0078a0001c0002t0002g0081 | 3 | HG01109.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1454-26717T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47189381 | ||||||
| chr16:47189507
|
T | C | 41 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1454-26843A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47189507 | ||||||
| chr16:47189549
|
G | C | 3 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0092 | 3 | HG02055.hp1 HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1454-26885C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47189549 | ||||||
| chr16:47189844
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1454-27180G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47189844 | ||||||
| chr16:47189922
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1454-27258G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47189922 | ||||||
| chr16:47190055
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1454-27391G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47190055 | ||||||
| chr16:47190261
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1454-27597T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47190261 | ||||||
| chr16:47190276
|
C | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1454-27612G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47190276 | ||||||
| chr16:47190604
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1454-27940G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47190604 | ||||||
| chr16:47190782
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG01169.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1453+28086T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47190782 | ||||||
| chr16:47191069
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1453+27799C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47191069 | ||||||
| chr16:47191118
|
G | A | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1453+27750C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47191118 | ||||||
| chr16:47191194
|
A | G | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1453+27674T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47191194 | ||||||
| chr16:47191556
|
A | C | 3 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0041 | 3 | HG02559.hp1 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1453+27312T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47191556 | ||||||
| chr16:47191584
|
C | T | 2 | a0001c0002t0001g0079a0001c0002t0001g0080 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1453+27284G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47191584 | ||||||
| chr16:47191806
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1453+27062G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47191806 | ||||||
| chr16:47192338
|
G | A | 1 | a0001c0002t0002g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1453+26530C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47192338 | ||||||
| chr16:47193094
|
C | CT | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1453+25773dupA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47193094 | ||||||
| chr16:47193130
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1453+25738G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47193130 | ||||||
| chr16:47193222
|
T | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.1453+25646A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47193222 | ||||||
| chr16:47193223
|
T | A | 8 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(5): Show | 8 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1453+25645A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47193223 | ||||||
| chr16:47193432
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0023 | 2 | HG00140.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1453+25436G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47193432 | ||||||
| chr16:47193967
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1453+24901T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47193967 | ||||||
| chr16:47194159
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1453+24709G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47194159 | ||||||
| chr16:47194703
|
A | AAT | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1453+24163_1453+24 others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47194703 | ||||||
| chr16:47195576
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1453+23292A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47195576 | ||||||
| chr16:47195598
|
T | C | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1453+23270A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47195598 | ||||||
| chr16:47196202
|
G | GT | 6 | a0001c0001t0001g0011a0001c0001t0001g0054a0001c0001t0001g0066others(3): Show | 6 | HG00609.hp2 HG00735.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1453+22665dupA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47196202 | ||||||
| chr16:47196249
|
A | T | 2 | a0001c0001t0003g0069a0001c0001t0003g0092 | 2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1453+22619T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47196249 | ||||||
| chr16:47196449
|
G | C | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1453+22419C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47196449 | ||||||
| chr16:47196594
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1453+22274C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47196594 | ||||||
| chr16:47196688
|
G | C | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1453+22180C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47196688 | ||||||
| chr16:47196916
|
C | T | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1453+21952G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47196916 | ||||||
| chr16:47197179
|
A | T | 41 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1453+21689T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47197179 | ||||||
| chr16:47197594
|
C | T | 1 | a0001c0003t0001g0001 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1453+21274G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47197594 | ||||||
| chr16:47198227
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1453+20641C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47198227 | ||||||
| chr16:47198453
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1453+20415A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47198453 | ||||||
| chr16:47198674
|
GT | G | 41 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1453+20193delA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47198674 | ||||||
| chr16:47198886
|
G | C | 2 | a0001c0002t0001g0079a0001c0002t0001g0080 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1453+19982C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47198886 | ||||||
| chr16:47199150
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1453+19718G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47199150 | ||||||
| chr16:47199209
|
G | A | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1453+19659C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47199209 | ||||||
| chr16:47199269
|
C | CCCAAACC others(3): Show |
98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(95): Show | 98 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.1453+19589_1453+19 others(16): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47199269 | ||||||
| chr16:47199269
|
C | CCCAAACC others(8): Show |
5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0003g0068others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1453+19584_1453+19 others(21): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47199269 | ||||||
| chr16:47199269
|
C | CCCAAACC others(13): Show |
4 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0091others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1453+19579_1453+19 others(26): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47199269 | ||||||
| chr16:47199641
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1453+19227A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47199641 | ||||||
| chr16:47199981
|
AGGTGGAG others(24): Show |
A | 20 | a0001c0002t0001g0094a0001c0002t0002g0072a0001c0002t0002g0073others(17): Show | 20 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1453+18856_1453+18 others(37): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47199981 | ||||||
| chr16:47200037
|
G | A | 3 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0092 | 3 | HG02055.hp1 HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1453+18831C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47200037 | ||||||
| chr16:47200074
|
T | A | 20 | a0001c0002t0001g0094a0001c0002t0002g0072a0001c0002t0002g0073others(17): Show | 20 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1453+18794A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47200074 | ||||||
| chr16:47200106
|
C | T | 2 | a0001c0002t0001g0079a0001c0002t0001g0080 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1453+18762G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47200106 | ||||||
| chr16:47200736
|
G | A | 2 | a0001c0002t0001g0079a0001c0002t0001g0080 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1453+18132C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47200736 | ||||||
| chr16:47201055
|
A | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0110 | 2 | HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1453+17813T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47201055 | ||||||
| chr16:47201207
|
AT | A | 36 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0100others(33): Show | 36 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1453+17660delA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47201207 | ||||||
| chr16:47201310
|
G | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1453+17558C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47201310 | ||||||
| chr16:47201356
|
C | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1453+17512G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47201356 | ||||||
| chr16:47201509
|
G | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1453+17359C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47201509 | ||||||
| chr16:47201527
|
C | T | 3 | a0001c0002t0002g0086a0001c0002t0002g0087a0001c0002t0002g0088 | 3 | HG00735.hp2 HG01074.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1453+17341G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47201527 | ||||||
| chr16:47201703
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1453+17165G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47201703 | ||||||
| chr16:47201735
|
T | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1453+17133A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47201735 | ||||||
| chr16:47201912
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1453+16956C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47201912 | ||||||
| chr16:47202090
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1453+16778C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47202090 | ||||||
| chr16:47202446
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0054 | 3 | HG00280.hp1 HG00609.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1453+16422G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47202446 | ||||||
| chr16:47203698
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0043 | 2 | HG01258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1453+15170C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47203698 | ||||||
| chr16:47204169
|
C | T | 41 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1453+14699G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47204169 | ||||||
| chr16:47204486
|
G | T | 10 | a0001c0002t0002g0072a0001c0002t0002g0075a0001c0002t0002g0076others(7): Show | 10 | HG01109.hp2 HG01891.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1453+14382C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47204486 | ||||||
| chr16:47204524
|
A | G | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1453+14344T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47204524 | ||||||
| chr16:47204549
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1453+14319G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47204549 | ||||||
| chr16:47204626
|
A | G | 3 | a0001c0002t0004g0064a0001c0002t0004g0065a0001c0002t0004g0095 | 3 | HG02895.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1453+14242T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47204626 | ||||||
| chr16:47204636
|
AAG | A | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1453+14230_1453+14 others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47204636 | ||||||
| chr16:47204928
|
A | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1453+13940T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47204928 | ||||||
| chr16:47205059
|
A | C | 2 | a0001c0002t0001g0079a0001c0002t0001g0080 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1453+13809T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47205059 | ||||||
| chr16:47205174
|
T | A | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1453+13694A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47205174 | ||||||
| chr16:47205178
|
C | T | 41 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1453+13690G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47205178 | ||||||
| chr16:47205241
|
C | T | 1 | a0001c0002t0002g0081 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1453+13627G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47205241 | ||||||
| chr16:47205616
|
A | C | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1453+13252T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47205616 | ||||||
| chr16:47205699
|
A | G | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1453+13169T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47205699 | ||||||
| chr16:47205828
|
T | TTATC | 8 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0026others(5): Show | 8 | HG00280.hp1 HG01074.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1453+13036_1453+13 others(10): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47205828 | ||||||
| chr16:47205828
|
T | TTATCTAT others(1): Show |
5 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(2): Show | 5 | HG01258.hp1 HG02258.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1453+13032_1453+13 others(14): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47205828 | ||||||
| chr16:47205828
|
TTATC | T | 31 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0020others(28): Show | 31 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1453+13036_1453+13 others(10): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47205828 | ||||||
| chr16:47205828
|
TTATCTAT others(1): Show |
T | 22 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0033others(19): Show | 22 | HG00642.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1453+13032_1453+13 others(14): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47205828 | ||||||
| chr16:47205828
|
TTATCTAT others(5): Show |
T | 6 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0042others(3): Show | 6 | HG00741.hp2 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1453+13028_1453+13 others(18): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47205828 | ||||||
| chr16:47205828
|
TTATCTAT others(9): Show |
T | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0002t0001g0079 | 3 | HG01496.hp2 HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1453+13024_1453+13 others(22): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47205828 | ||||||
| chr16:47205828
|
TTATCTAT others(17): Show |
T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0034 | 3 | HG01169.hp2 HG02602.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1453+13016_1453+13 others(30): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47205828 | ||||||
| chr16:47205854
|
A | C | 1 | a0001c0002t0001g0067 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1453+13014T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47205854 | ||||||
| chr16:47205936
|
G | A | 1 | a0001c0004t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1453+12932C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47205936 | ||||||
| chr16:47206019
|
C | T | 1 | a0001c0004t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1453+12849G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47206019 | ||||||
| chr16:47206272
|
C | G | 1 | a0001c0002t0002g0078 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1453+12596G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47206272 | ||||||
| chr16:47206466
|
C | A | 1 | a0001c0001t0001g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1453+12402G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47206466 | ||||||
| chr16:47206645
|
G | T | 2 | a0001c0002t0002g0073a0001c0002t0002g0074 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1453+12223C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47206645 | ||||||
| chr16:47207375
|
C | T | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1453+11493G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47207375 | ||||||
| chr16:47207406
|
G | A | 1 | a0001c0004t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1453+11462C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47207406 | ||||||
| chr16:47208027
|
TTAAA | T | 3 | a0001c0002t0002g0075a0001c0002t0002g0076a0001c0002t0002g0085 | 3 | HG01891.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1453+10837_1453+10 others(10): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47208027 | ||||||
| chr16:47208279
|
T | A | 1 | a0001c0001t0001g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1453+10589A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47208279 | ||||||
| chr16:47208764
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1453+10104C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47208764 | ||||||
| chr16:47209061
|
T | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1453+9807A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47209061 | ||||||
| chr16:47209158
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1453+9710T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47209158 | ||||||
| chr16:47209226
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0051 | 2 | HG00741.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1453+9642G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47209226 | ||||||
| chr16:47209886
|
G | T | 1 | a0001c0001t0001g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1453+8982C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47209886 | ||||||
| chr16:47211008
|
C | T | 2 | a0001c0002t0002g0073a0001c0002t0002g0074 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1453+7860G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47211008 | ||||||
| chr16:47211185
|
G | C | 41 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1453+7683C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47211185 | ||||||
| chr16:47211621
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1453+7247G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47211621 | ||||||
| chr16:47212789
|
G | A | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1453+6079C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47212789 | ||||||
| chr16:47213730
|
C | G | 1 | a0001c0001t0001g0039 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1453+5138G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47213730 | ||||||
| chr16:47214162
|
C | CA | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG01496.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1453+4705dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47214162 | ||||||
| chr16:47214281
|
G | T | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1453+4587C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47214281 | ||||||
| chr16:47214824
|
ATGT | A | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1453+4041_1453+404 others(7): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47214824 | ||||||
| chr16:47214921
|
A | AAC | 7 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0018others(4): Show | 7 | HG00741.hp2 HG01891.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1453+3945_1453+394 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47214921 | ||||||
| chr16:47214921
|
AAC | A | 22 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(19): Show | 22 | HG00140.hp2 HG00280.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.1453+3945_1453+394 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47214921 | ||||||
| chr16:47214921
|
AACAC | A | 33 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0037others(30): Show | 33 | HG00735.hp1 HG00735.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1453+3943_1453+394 others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47214921 | ||||||
| chr16:47214921
|
AACACAC | A | 10 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0054others(7): Show | 10 | HG00609.hp2 HG01496.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1453+3941_1453+394 others(10): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47214921 | ||||||
| chr16:47214921
|
AACACACA others(1): Show |
A | 4 | a0001c0001t0001g0026a0001c0001t0001g0061a0001c0002t0002g0073others(1): Show | 4 | HG01074.hp1 HG02723.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1453+3939_1453+394 others(12): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47214921 | ||||||
| chr16:47216050
|
C | T | 41 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1453+2818G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47216050 | ||||||
| chr16:47216085
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1453+2783G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47216085 | ||||||
| chr16:47216152
|
A | AG | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1453+2715dupC | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47216152 | ||||||
| chr16:47216443
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0023 | 2 | HG00140.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1453+2425G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47216443 | ||||||
| chr16:47216444
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1453+2424C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47216444 | ||||||
| chr16:47216591
|
C | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0063 | 2 | HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1453+2277G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47216591 | ||||||
| chr16:47216668
|
A | AT | 2 | a0001c0002t0002g0078a0001c0002t0002g0081 | 2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1453+2199dupA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47216668 | ||||||
| chr16:47216672
|
A | T | 34 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(31): Show | 34 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1453+2196T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47216672 | ||||||
| chr16:47216676
|
T | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0003g0097 | 3 | HG01361.hp2 HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1453+2192A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47216676 | ||||||
| chr16:47217104
|
T | C | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.1453+1764A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47217104 | ||||||
| chr16:47217144
|
G | GA | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.1453+1723dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47217144 | ||||||
| chr16:47217155
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1453+1713T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47217155 | ||||||
| chr16:47217233
|
C | T | 1 | a0001c0002t0002g0093 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1453+1635G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47217233 | ||||||
| chr16:47217430
|
T | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1453+1438A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47217430 | ||||||
| chr16:47217546
|
G | T | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1453+1322C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47217546 | ||||||
| chr16:47218156
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1453+712G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47218156 | ||||||
| chr16:47218593
|
G | C | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1453+275C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47218593 | ||||||
| chr16:47218771
|
A | G | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1453+97T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47218771 | ||||||
| chr16:47218829
|
G | T | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1453+39C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 14/17 | chr16 | 47218829 | ||||||
| chr16:47219597
|
A | G | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1375-651T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47219597 | ||||||
| chr16:47220595
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1375-1649C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47220595 | ||||||
| chr16:47220667
|
C | T | 2 | a0001c0002t0002g0078a0001c0002t0002g0081 | 2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1375-1721G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47220667 | ||||||
| chr16:47221146
|
C | T | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1375-2200G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47221146 | ||||||
| chr16:47221876
|
G | C | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1375-2930C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47221876 | ||||||
| chr16:47222337
|
A | G | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.1375-3391T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47222337 | ||||||
| chr16:47222413
|
C | CT | 32 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0091others(29): Show | 32 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1375-3468dupA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47222413 | ||||||
| chr16:47222419
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1375-3473A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47222419 | ||||||
| chr16:47222436
|
C | T | 4 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0091others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1375-3490G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47222436 | ||||||
| chr16:47222476
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1375-3530G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47222476 | ||||||
| chr16:47222482
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1375-3536G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47222482 | ||||||
| chr16:47222655
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1375-3709G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47222655 | ||||||
| chr16:47222741
|
A | C | 20 | a0001c0002t0001g0094a0001c0002t0002g0072a0001c0002t0002g0073others(17): Show | 20 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1375-3795T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47222741 | ||||||
| chr16:47222754
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1375-3808A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47222754 | ||||||
| chr16:47223306
|
A | G | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1375-4360T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47223306 | ||||||
| chr16:47223571
|
G | A | 10 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0026others(7): Show | 10 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.1375-4625C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47223571 | ||||||
| chr16:47223702
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1375-4756C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47223702 | ||||||
| chr16:47223827
|
G | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1375-4881C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47223827 | ||||||
| chr16:47224070
|
T | TG | 20 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0022others(17): Show | 20 | HG00642.hp2 HG00735.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1375-5125dupC | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47224070 | ||||||
| chr16:47224487
|
C | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0054 | 2 | HG00609.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1375-5541G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47224487 | ||||||
| chr16:47224589
|
C | T | 1 | a0001c0002t0001g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1375-5643G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47224589 | ||||||
| chr16:47225219
|
T | C | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1375-6273A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47225219 | ||||||
| chr16:47225621
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1375-6675C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47225621 | ||||||
| chr16:47226040
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1375-7094A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47226040 | ||||||
| chr16:47226563
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1375-7617C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47226563 | ||||||
| chr16:47227851
|
G | A | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1375-8905C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47227851 | ||||||
| chr16:47228353
|
GT | G | 38 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(35): Show | 38 | HG00735.hp2 HG01074.hp2 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.1375-9408delA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47228353 | ||||||
| chr16:47228364
|
G | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1375-9418C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47228364 | ||||||
| chr16:47228413
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1375-9467G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47228413 | ||||||
| chr16:47228420
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0051 | 2 | HG00741.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1375-9474G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47228420 | ||||||
| chr16:47228932
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1374+9033A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47228932 | ||||||
| chr16:47228978
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1374+8987T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47228978 | ||||||
| chr16:47229065
|
T | C | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1374+8900A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47229065 | ||||||
| chr16:47229592
|
T | A | 1 | a0001c0001t0001g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1374+8373A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47229592 | ||||||
| chr16:47229855
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1374+8110G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47229855 | ||||||
| chr16:47229943
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1374+8022A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47229943 | ||||||
| chr16:47230247
|
T | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0023 | 2 | HG00140.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1374+7718A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47230247 | ||||||
| chr16:47230249
|
G | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0023 | 2 | HG00140.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1374+7716C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47230249 | ||||||
| chr16:47230710
|
G | T | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1374+7255C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47230710 | ||||||
| chr16:47231030
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1374+6935C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47231030 | ||||||
| chr16:47231534
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1374+6431G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47231534 | ||||||
| chr16:47232000
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1374+5965G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47232000 | ||||||
| chr16:47232004
|
A | C | 1 | a0001c0004t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1374+5961T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47232004 | ||||||
| chr16:47232637
|
G | GT | 7 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(4): Show | 7 | HG00741.hp2 HG01169.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1374+5327dupA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47232637 | ||||||
| chr16:47232655
|
T | C | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1374+5310A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47232655 | ||||||
| chr16:47232823
|
T | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1374+5142A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47232823 | ||||||
| chr16:47232976
|
A | G | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1374+4989T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47232976 | ||||||
| chr16:47234053
|
G | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0023 | 2 | HG00140.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1374+3912C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47234053 | ||||||
| chr16:47234088
|
A | C | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1374+3877T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47234088 | ||||||
| chr16:47234295
|
G | C | 1 | a0001c0001t0001g0006 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1374+3670C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47234295 | ||||||
| chr16:47234620
|
G | T | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1374+3345C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47234620 | ||||||
| chr16:47234706
|
T | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1374+3259A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47234706 | ||||||
| chr16:47234802
|
T | C | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1374+3163A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47234802 | ||||||
| chr16:47234840
|
G | T | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1374+3125C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47234840 | ||||||
| chr16:47234841
|
T | G | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1374+3124A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47234841 | ||||||
| chr16:47234932
|
G | C | 1 | a0001c0001t0003g0092 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1374+3033C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47234932 | ||||||
| chr16:47235268
|
T | TA | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(1): Show | 4 | HG01361.hp2 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1374+2696dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47235268 | ||||||
| chr16:47235295
|
G | T | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1374+2670C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47235295 | ||||||
| chr16:47235727
|
G | C | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1374+2238C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47235727 | ||||||
| chr16:47235751
|
A | G | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1374+2214T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47235751 | ||||||
| chr16:47236047
|
T | C | 45 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(42): Show | 45 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.1374+1918A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47236047 | ||||||
| chr16:47236400
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1374+1565G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47236400 | ||||||
| chr16:47236474
|
CA | C | 36 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0027others(33): Show | 36 | HG00735.hp2 HG01109.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.1374+1490delT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47236474 | ||||||
| chr16:47237597
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1374+368G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47237597 | ||||||
| chr16:47237679
|
C | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1374+286G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 13/17 | chr16 | 47237679 | ||||||
| chr16:47238467
|
G | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1331-459C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47238467 | ||||||
| chr16:47238487
|
T | C | 1 | a0001c0002t0001g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1331-479A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47238487 | ||||||
| chr16:47239163
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1331-1155C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47239163 | ||||||
| chr16:47239341
|
C | G | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1331-1333G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47239341 | ||||||
| chr16:47239355
|
C | G | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1331-1347G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47239355 | ||||||
| chr16:47239390
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1331-1382C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47239390 | ||||||
| chr16:47239482
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1331-1474T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47239482 | ||||||
| chr16:47239515
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | HG02922.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1331-1507A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47239515 | ||||||
| chr16:47239733
|
C | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1331-1725G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47239733 | ||||||
| chr16:47239885
|
G | A | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1331-1877C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47239885 | ||||||
| chr16:47240129
|
G | GA | 4 | a0001c0001t0001g0030a0001c0001t0001g0104a0001c0001t0001g0105others(1): Show | 4 | HG02055.hp2 HG02280.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1331-2122dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47240129 | ||||||
| chr16:47240129
|
GA | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0055a0001c0001t0001g0056others(1): Show | 4 | HG01255.hp1 HG02922.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1331-2122delT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47240129 | ||||||
| chr16:47240161
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1331-2153C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47240161 | ||||||
| chr16:47240295
|
C | CA | 19 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0032others(16): Show | 19 | HG00280.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1331-2288dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47240295 | ||||||
| chr16:47240955
|
T | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1331-2947A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47240955 | ||||||
| chr16:47240972
|
T | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0050 | 2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1331-2964A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47240972 | ||||||
| chr16:47241068
|
TA | T | 40 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(37): Show | 40 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.1331-3061delT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47241068 | ||||||
| chr16:47241325
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1331-3317A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47241325 | ||||||
| chr16:47241683
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1331-3675G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47241683 | ||||||
| chr16:47241949
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1331-3941C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47241949 | ||||||
| chr16:47241953
|
C | CA | 6 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0049others(3): Show | 6 | HG01169.hp2 HG02109.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1331-3946dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47241953 | ||||||
| chr16:47242012
|
G | A | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1331-4004C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47242012 | ||||||
| chr16:47242054
|
C | T | 3 | a0001c0002t0004g0064a0001c0002t0004g0065a0001c0002t0004g0095 | 3 | HG02895.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1331-4046G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47242054 | ||||||
| chr16:47242131
|
C | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1331-4123G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47242131 | ||||||
| chr16:47242333
|
C | CA | 10 | a0001c0002t0002g0072a0001c0002t0002g0075a0001c0002t0002g0076others(7): Show | 10 | HG01109.hp2 HG01891.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1331-4326dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47242333 | ||||||
| chr16:47242533
|
T | A | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1331-4525A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47242533 | ||||||
| chr16:47242592
|
T | C | 5 | a0001c0001t0001g0031a0001c0001t0001g0058a0001c0001t0001g0061others(2): Show | 5 | HG00642.hp2 HG02735.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1331-4584A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47242592 | ||||||
| chr16:47242853
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1331-4845A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47242853 | ||||||
| chr16:47242909
|
G | T | 70 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(67): Show | 70 | HG00140.hp2 HG00609.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.1331-4901C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47242909 | ||||||
| chr16:47242934
|
C | T | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1331-4926G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47242934 | ||||||
| chr16:47242970
|
A | G | 24 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(21): Show | 24 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.1331-4962T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47242970 | ||||||
| chr16:47243090
|
T | G | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1331-5082A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47243090 | ||||||
| chr16:47243110
|
CAT | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1331-5104_1331-510 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47243110 | ||||||
| chr16:47243164
|
A | C | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1331-5156T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47243164 | ||||||
| chr16:47244102
|
T | A | 1 | a0001c0001t0001g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1331-6094A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47244102 | ||||||
| chr16:47244337
|
T | A | 3 | a0001c0002t0002g0072a0001c0002t0002g0078a0001c0002t0002g0081 | 3 | HG01109.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1331-6329A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47244337 | ||||||
| chr16:47244381
|
A | C | 1 | a0001c0001t0003g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1331-6373T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47244381 | ||||||
| chr16:47244415
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1331-6407A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47244415 | ||||||
| chr16:47244453
|
G | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1331-6445C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47244453 | ||||||
| chr16:47244589
|
TTTTGTGT others(3): Show |
T | 1 | a0001c0001t0001g0004 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1331-6591_1331-658 others(14): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47244589 | ||||||
| chr16:47244590
|
TTTGTGTG others(4): Show |
T | 2 | a0001c0001t0001g0033a0001c0001t0001g0110 | 2 | HG00642.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1331-6593_1331-658 others(15): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47244590 | ||||||
| chr16:47244591
|
TTG | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0060 | 2 | HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1331-6585_1331-658 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47244591 | ||||||
| chr16:47244591
|
TTGTG | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0011others(2): Show | 5 | HG02602.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1331-6587_1331-658 others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47244591 | ||||||
| chr16:47244591
|
TTGTGTG | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0063 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1331-6589_1331-658 others(10): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47244591 | ||||||
| chr16:47244591
|
TTGTGTGT others(1): Show |
T | 11 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0022others(8): Show | 11 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.1331-6591_1331-658 others(12): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47244591 | ||||||
| chr16:47244591
|
TTGTGTGT others(3): Show |
T | 24 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(21): Show | 24 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.1331-6593_1331-658 others(14): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47244591 | ||||||
| chr16:47244591
|
TTGTGTGT others(5): Show |
T | 10 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0019others(7): Show | 10 | HG00140.hp1 HG00741.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.1331-6595_1331-658 others(16): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47244591 | ||||||
| chr16:47244591
|
TTGTGTGT others(7): Show |
T | 6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0066others(3): Show | 6 | HG01496.hp1 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1331-6597_1331-658 others(18): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47244591 | ||||||
| chr16:47244591
|
TTGTGTGT others(9): Show |
T | 28 | a0001c0001t0001g0050a0001c0001t0001g0059a0001c0001t0001g0100others(25): Show | 28 | HG01109.hp1 HG01109.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.1331-6599_1331-658 others(20): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47244591 | ||||||
| chr16:47244591
|
TTGTGTGT others(11): Show |
T | 12 | a0001c0001t0001g0018a0001c0001t0003g0069a0001c0001t0003g0070others(9): Show | 12 | HG00735.hp2 HG01074.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1331-6601_1331-658 others(22): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47244591 | ||||||
| chr16:47244591
|
TTGTGTGT others(13): Show |
T | 1 | a0001c0004t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1331-6603_1331-658 others(24): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47244591 | ||||||
| chr16:47244615
|
G | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG01496.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1331-6607C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47244615 | ||||||
| chr16:47244883
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1331-6875T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47244883 | ||||||
| chr16:47245026
|
C | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1331-7018G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47245026 | ||||||
| chr16:47245068
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1331-7060G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47245068 | ||||||
| chr16:47245764
|
T | A | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1331-7756A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47245764 | ||||||
| chr16:47245770
|
T | C | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1331-7762A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47245770 | ||||||
| chr16:47247026
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0043 | 2 | HG01258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1331-9018G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47247026 | ||||||
| chr16:47247326
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1331-9318C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47247326 | ||||||
| chr16:47247571
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1331-9563C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47247571 | ||||||
| chr16:47247622
|
C | T | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1331-9614G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47247622 | ||||||
| chr16:47247838
|
G | A | 1 | a0001c0004t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1331-9830C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47247838 | ||||||
| chr16:47247842
|
C | T | 35 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(32): Show | 35 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.1331-9834G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47247842 | ||||||
| chr16:47248074
|
T | TA | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.1331-10067dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47248074 | ||||||
| chr16:47249499
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1330+9133T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47249499 | ||||||
| chr16:47249708
|
A | G | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG00735.hp1 HG01169.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1330+8924T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47249708 | ||||||
| chr16:47249732
|
GT | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1330+8899delA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47249732 | ||||||
| chr16:47250066
|
T | C | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.1330+8566A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47250066 | ||||||
| chr16:47250579
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1330+8053T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47250579 | ||||||
| chr16:47250649
|
A | G | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1330+7983T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47250649 | ||||||
| chr16:47250781
|
A | C | 1 | a0001c0002t0002g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1330+7851T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47250781 | ||||||
| chr16:47251263
|
C | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1330+7369G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47251263 | ||||||
| chr16:47251423
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1330+7209C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47251423 | ||||||
| chr16:47252394
|
G | A | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1330+6238C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47252394 | ||||||
| chr16:47252490
|
A | G | 1 | a0001c0001t0003g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1330+6142T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47252490 | ||||||
| chr16:47252612
|
C | T | 1 | a0001c0002t0001g0079 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1330+6020G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47252612 | ||||||
| chr16:47253277
|
C | G | 1 | a0001c0001t0003g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1330+5355G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47253277 | ||||||
| chr16:47254407
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1330+4225G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47254407 | ||||||
| chr16:47254408
|
A | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1330+4224T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47254408 | ||||||
| chr16:47254430
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1330+4202A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47254430 | ||||||
| chr16:47254766
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1330+3866A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47254766 | ||||||
| chr16:47254947
|
C | G | 10 | a0001c0002t0002g0072a0001c0002t0002g0075a0001c0002t0002g0076others(7): Show | 10 | HG01109.hp2 HG01891.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1330+3685G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47254947 | ||||||
| chr16:47255738
|
G | A | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1330+2894C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47255738 | ||||||
| chr16:47255776
|
T | A | 2 | a0001c0002t0004g0064a0001c0002t0004g0065 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1330+2856A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47255776 | ||||||
| chr16:47256248
|
T | G | 1 | a0001c0001t0001g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1330+2384A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47256248 | ||||||
| chr16:47256297
|
C | G | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1330+2335G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47256297 | ||||||
| chr16:47256516
|
T | C | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1330+2116A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47256516 | ||||||
| chr16:47257104
|
G | A | 41 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1330+1528C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47257104 | ||||||
| chr16:47258217
|
G | C | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1330+415C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 12/17 | chr16 | 47258217 | ||||||
| chr16:47258905
|
C | A | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.1222-165G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 11/17 | chr16 | 47258905 | ||||||
| chr16:47259330
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1222-590G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 11/17 | chr16 | 47259330 | ||||||
| chr16:47259441
|
T | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1222-701A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 11/17 | chr16 | 47259441 | ||||||
| chr16:47260100
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1221+445C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 11/17 | chr16 | 47260100 | ||||||
| chr16:47260514
|
C | T | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1221+31G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 11/17 | chr16 | 47260514 | ||||||
| chr16:47260937
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1071-242A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47260937 | ||||||
| chr16:47261007
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1071-312G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47261007 | ||||||
| chr16:47262228
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1071-1533A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47262228 | ||||||
| chr16:47262828
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1071-2133T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47262828 | ||||||
| chr16:47263223
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1071-2528G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47263223 | ||||||
| chr16:47263337
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1071-2642T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47263337 | ||||||
| chr16:47263683
|
T | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1071-2988A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47263683 | ||||||
| chr16:47263725
|
C | CTGAA | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1071-3034_1071-303 others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47263725 | ||||||
| chr16:47263821
|
C | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1071-3126G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47263821 | ||||||
| chr16:47264112
|
C | A | 2 | a0001c0002t0001g0079a0001c0002t0001g0080 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1071-3417G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47264112 | ||||||
| chr16:47264239
|
A | T | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.1071-3544T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47264239 | ||||||
| chr16:47264545
|
T | TAC | 12 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0020others(9): Show | 12 | HG00280.hp2 HG00609.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1071-3852_1071-385 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47264545 | ||||||
| chr16:47264545
|
T | TACAC | 11 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0018others(8): Show | 11 | HG00741.hp2 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1071-3854_1071-385 others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47264545 | ||||||
| chr16:47264545
|
T | TACACAC | 4 | a0001c0001t0001g0009a0001c0001t0003g0068a0001c0002t0002g0084others(1): Show | 4 | HG02258.hp2 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1071-3856_1071-385 others(10): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47264545 | ||||||
| chr16:47264545
|
TAC | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | HG00609.hp2 HG00642.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.1071-3852_1071-385 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47264545 | ||||||
| chr16:47264545
|
TACAC | T | 13 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(10): Show | 13 | HG00140.hp2 HG01169.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.1071-3854_1071-385 others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47264545 | ||||||
| chr16:47264545
|
TACACAC | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0109a0001c0002t0001g0067 | 3 | HG00735.hp1 HG01496.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1071-3856_1071-385 others(10): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47264545 | ||||||
| chr16:47264545
|
TACACACA others(1): Show |
T | 2 | a0001c0001t0001g0060a0001c0002t0001g0096 | 2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1071-3858_1071-385 others(12): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47264545 | ||||||
| chr16:47264545
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1071-3860_1071-385 others(14): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47264545 | ||||||
| chr16:47264545
|
TACACACA others(9): Show |
T | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1071-3866_1071-385 others(20): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47264545 | ||||||
| chr16:47264798
|
T | C | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1071-4103A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47264798 | ||||||
| chr16:47265103
|
C | CTATTAT | 2 | a0001c0001t0001g0002a0001c0001t0001g0063 | 2 | HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1071-4414_1071-440 others(10): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47265103 | ||||||
| chr16:47265178
|
AT | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.1071-4484delA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47265178 | ||||||
| chr16:47265560
|
C | T | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1071-4865G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47265560 | ||||||
| chr16:47265571
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1071-4876T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47265571 | ||||||
| chr16:47265750
|
C | A | 1 | a0001c0003t0001g0001 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1071-5055G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47265750 | ||||||
| chr16:47266240
|
T | TG | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1071-5546dupC | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47266240 | ||||||
| chr16:47266249
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1071-5554C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47266249 | ||||||
| chr16:47266364
|
C | T | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1071-5669G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47266364 | ||||||
| chr16:47266586
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1071-5891C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47266586 | ||||||
| chr16:47266700
|
G | C | 1 | a0001c0002t0002g0077 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1071-6005C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47266700 | ||||||
| chr16:47266949
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1071-6254G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47266949 | ||||||
| chr16:47267081
|
G | A | 35 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(32): Show | 35 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.1071-6386C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47267081 | ||||||
| chr16:47267176
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1071-6481A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47267176 | ||||||
| chr16:47267338
|
T | C | 1 | a0001c0002t0002g0077 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1071-6643A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47267338 | ||||||
| chr16:47267423
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1071-6728A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47267423 | ||||||
| chr16:47267591
|
C | T | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1071-6896G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47267591 | ||||||
| chr16:47267880
|
C | A | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1071-7185G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47267880 | ||||||
| chr16:47268302
|
G | A | 4 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0091others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1071-7607C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47268302 | ||||||
| chr16:47268438
|
G | C | 1 | a0001c0001t0001g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1071-7743C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47268438 | ||||||
| chr16:47268921
|
T | A | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1071-8226A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47268921 | ||||||
| chr16:47269141
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1071-8446T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47269141 | ||||||
| chr16:47269486
|
T | TA | 35 | a0001c0001t0001g0058a0001c0001t0001g0066a0001c0001t0001g0100others(32): Show | 35 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.1071-8792dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47269486 | ||||||
| chr16:47269486
|
T | TAA | 8 | a0001c0001t0001g0106a0001c0001t0003g0068a0001c0001t0003g0069others(5): Show | 8 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1071-8793_1071-879 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47269486 | ||||||
| chr16:47269657
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0051 | 2 | HG00741.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1071-8962G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47269657 | ||||||
| chr16:47269724
|
T | G | 26 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(23): Show | 26 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.1071-9029A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47269724 | ||||||
| chr16:47269927
|
C | T | 9 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0026others(6): Show | 9 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.1071-9232G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47269927 | ||||||
| chr16:47270357
|
CAAT | C | 9 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0026others(6): Show | 9 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.1071-9665_1071-966 others(7): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47270357 | ||||||
| chr16:47270586
|
G | C | 2 | a0001c0002t0002g0073a0001c0002t0002g0074 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1071-9891C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47270586 | ||||||
| chr16:47270835
|
A | C | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1071-10140T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47270835 | ||||||
| chr16:47270839
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1071-10144T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47270839 | ||||||
| chr16:47270842
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1071-10147T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47270842 | ||||||
| chr16:47270846
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1071-10151C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47270846 | ||||||
| chr16:47270848
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1071-10153T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47270848 | ||||||
| chr16:47270853
|
C | G | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1071-10158G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47270853 | ||||||
| chr16:47270858
|
T | A | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1071-10163A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47270858 | ||||||
| chr16:47270859
|
A | C | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1071-10164T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47270859 | ||||||
| chr16:47270868
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1071-10173G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47270868 | ||||||
| chr16:47270944
|
G | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG00735.hp1 HG01169.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1071-10249C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47270944 | ||||||
| chr16:47271736
|
G | A | 9 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0026others(6): Show | 9 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.1071-11041C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47271736 | ||||||
| chr16:47272133
|
T | C | 27 | a0001c0002t0001g0067a0001c0002t0001g0079a0001c0002t0001g0080others(24): Show | 27 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1071-11438A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47272133 | ||||||
| chr16:47272263
|
T | C | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1071-11568A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47272263 | ||||||
| chr16:47272372
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1071-11677G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47272372 | ||||||
| chr16:47272494
|
G | C | 3 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0092 | 3 | HG02055.hp1 HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1071-11799C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47272494 | ||||||
| chr16:47272545
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1071-11850C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47272545 | ||||||
| chr16:47272687
|
C | T | 1 | a0001c0002t0001g0067 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1071-11992G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47272687 | ||||||
| chr16:47273122
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1071-12427A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47273122 | ||||||
| chr16:47273236
|
A | G | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1071-12541T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47273236 | ||||||
| chr16:47273355
|
A | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1071-12660T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47273355 | ||||||
| chr16:47273510
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1071-12815A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47273510 | ||||||
| chr16:47273556
|
A | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0023 | 2 | HG00140.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1071-12861T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47273556 | ||||||
| chr16:47273632
|
A | T | 1 | a0001c0001t0001g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1071-12937T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47273632 | ||||||
| chr16:47273790
|
G | GTTTA | 17 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.1071-13099_1071-13 others(10): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47273790 | ||||||
| chr16:47273790
|
GTTTA | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1071-13099_1071-13 others(10): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47273790 | ||||||
| chr16:47273792
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1071-13097A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47273792 | ||||||
| chr16:47273994
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1071-13299G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47273994 | ||||||
| chr16:47274148
|
T | G | 3 | a0001c0001t0001g0031a0001c0001t0001g0058a0001c0003t0001g0001 | 3 | HG00642.hp2 HG02735.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1071-13453A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47274148 | ||||||
| chr16:47274249
|
C | T | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1071-13554G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47274249 | ||||||
| chr16:47274303
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1071-13608T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47274303 | ||||||
| chr16:47274340
|
T | C | 1 | a0001c0002t0001g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1071-13645A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47274340 | ||||||
| chr16:47274637
|
A | C | 2 | a0001c0002t0001g0079a0001c0002t0001g0080 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1071-13942T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47274637 | ||||||
| chr16:47274745
|
G | GT | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1071-14051dupA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47274745 | ||||||
| chr16:47277027
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1071-16332G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47277027 | ||||||
| chr16:47277189
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1071-16494A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47277189 | ||||||
| chr16:47277417
|
A | C | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1071-16722T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47277417 | ||||||
| chr16:47277469
|
G | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG00735.hp1 HG01169.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1071-16774C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47277469 | ||||||
| chr16:47277634
|
T | A | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1071-16939A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47277634 | ||||||
| chr16:47277657
|
G | C | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1071-16962C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47277657 | ||||||
| chr16:47277660
|
A | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1071-16965T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47277660 | ||||||
| chr16:47278164
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1071-17469G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47278164 | ||||||
| chr16:47278269
|
A | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1071-17574T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47278269 | ||||||
| chr16:47279427
|
T | C | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1071-18732A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47279427 | ||||||
| chr16:47279819
|
T | A | 1 | a0001c0001t0001g0033 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1071-19124A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47279819 | ||||||
| chr16:47280515
|
T | G | 1 | a0001c0001t0001g0052 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1071-19820A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47280515 | ||||||
| chr16:47280744
|
C | T | 1 | a0001c0002t0001g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1071-20049G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47280744 | ||||||
| chr16:47281397
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1071-20702A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47281397 | ||||||
| chr16:47282462
|
T | C | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.1071-21767A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47282462 | ||||||
| chr16:47282612
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1071-21917A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47282612 | ||||||
| chr16:47282708
|
A | G | 3 | a0001c0002t0004g0064a0001c0002t0004g0065a0001c0002t0004g0095 | 3 | HG02895.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1071-22013T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47282708 | ||||||
| chr16:47283257
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1071-22562A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47283257 | ||||||
| chr16:47284424
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1071-23729C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47284424 | ||||||
| chr16:47284451
|
A | C | 2 | a0001c0002t0002g0078a0001c0002t0002g0081 | 2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1071-23756T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47284451 | ||||||
| chr16:47284851
|
T | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1071-24156A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47284851 | ||||||
| chr16:47285363
|
A | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG01496.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1071-24668T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47285363 | ||||||
| chr16:47285443
|
C | A | 1 | a0001c0002t0001g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1071-24748G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47285443 | ||||||
| chr16:47285490
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1071-24795T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47285490 | ||||||
| chr16:47285568
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1071-24873T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47285568 | ||||||
| chr16:47285962
|
A | C | 1 | a0001c0002t0001g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1071-25267T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47285962 | ||||||
| chr16:47286077
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1070+25163A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47286077 | ||||||
| chr16:47286284
|
G | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0058a0001c0003t0001g0001 | 3 | HG00642.hp2 HG02735.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1070+24956C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47286284 | ||||||
| chr16:47286366
|
G | A | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1070+24874C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47286366 | ||||||
| chr16:47286798
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1070+24442A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47286798 | ||||||
| chr16:47286853
|
T | C | 38 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(35): Show | 38 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1070+24387A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47286853 | ||||||
| chr16:47287503
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1070+23737G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47287503 | ||||||
| chr16:47287725
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1070+23515A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47287725 | ||||||
| chr16:47287755
|
T | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1070+23485A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47287755 | ||||||
| chr16:47287899
|
A | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1070+23341T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47287899 | ||||||
| chr16:47288305
|
C | T | 41 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1070+22935G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47288305 | ||||||
| chr16:47288368
|
A | G | 1 | a0001c0001t0003g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1070+22872T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47288368 | ||||||
| chr16:47288413
|
A | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1070+22827T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47288413 | ||||||
| chr16:47288618
|
T | A | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1070+22622A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47288618 | ||||||
| chr16:47288691
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0023 | 3 | HG00140.hp2 HG00280.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1070+22549C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47288691 | ||||||
| chr16:47289206
|
T | G | 3 | a0001c0002t0002g0086a0001c0002t0002g0087a0001c0002t0002g0088 | 3 | HG00735.hp2 HG01074.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1070+22034A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47289206 | ||||||
| chr16:47289311
|
T | A | 1 | a0001c0001t0001g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1070+21929A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47289311 | ||||||
| chr16:47289423
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1070+21817T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47289423 | ||||||
| chr16:47289429
|
G | T | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1070+21811C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47289429 | ||||||
| chr16:47290569
|
T | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0038others(3): Show | 6 | HG02055.hp2 HG02559.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1070+20671A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47290569 | ||||||
| chr16:47290621
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0043 | 2 | HG01258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1070+20619C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47290621 | ||||||
| chr16:47291020
|
GC | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1070+20219delG | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47291020 | ||||||
| chr16:47291155
|
A | G | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1070+20085T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47291155 | ||||||
| chr16:47291336
|
C | T | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1070+19904G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47291336 | ||||||
| chr16:47291833
|
T | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1070+19407A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47291833 | ||||||
| chr16:47292060
|
C | T | 1 | a0001c0004t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1070+19180G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47292060 | ||||||
| chr16:47292481
|
G | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1070+18759C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47292481 | ||||||
| chr16:47293028
|
A | C | 7 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(4): Show | 7 | HG00735.hp1 HG01169.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1070+18212T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47293028 | ||||||
| chr16:47293075
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1070+18165A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47293075 | ||||||
| chr16:47293181
|
A | AATGATAT others(22): Show |
30 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(27): Show | 30 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1070+18030_1070+18 others(35): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47293181 | ||||||
| chr16:47293181
|
A | AATGATAT others(51): Show |
1 | a0001c0002t0001g0067 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1070+18058_1070+18 others(64): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47293181 | ||||||
| chr16:47293192
|
T | TTATATAT others(28): Show |
1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1070+18013_1070+18 others(41): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47293192 | ||||||
| chr16:47293232
|
T | TATC | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.1070+18007_1070+18 others(9): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47293232 | ||||||
| chr16:47293327
|
T | C | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1070+17913A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47293327 | ||||||
| chr16:47293587
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1070+17653G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47293587 | ||||||
| chr16:47293612
|
C | T | 31 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(28): Show | 31 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.1070+17628G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47293612 | ||||||
| chr16:47293613
|
AT | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1070+17626delA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47293613 | ||||||
| chr16:47294447
|
A | T | 38 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(35): Show | 38 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1070+16793T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47294447 | ||||||
| chr16:47295061
|
T | A | 1 | a0001c0001t0001g0027 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1070+16179A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47295061 | ||||||
| chr16:47295222
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1070+16018A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47295222 | ||||||
| chr16:47295432
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG00735.hp1 HG01169.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1070+15808G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47295432 | ||||||
| chr16:47295661
|
T | C | 1 | a0001c0002t0002g0077 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1070+15579A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47295661 | ||||||
| chr16:47296068
|
T | TTTTTA | 28 | a0001c0001t0001g0031a0001c0001t0001g0058a0001c0001t0001g0100others(25): Show | 28 | HG00642.hp2 HG00735.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.1070+15167_1070+15 others(11): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47296068 | ||||||
| chr16:47296068
|
T | TTTTTATT others(3): Show |
3 | a0001c0001t0001g0105a0001c0002t0004g0064a0001c0002t0004g0065 | 3 | HG02280.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1070+15162_1070+15 others(16): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47296068 | ||||||
| chr16:47296068
|
T | TTTTTATT others(8): Show |
1 | a0001c0004t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1070+15157_1070+15 others(21): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47296068 | ||||||
| chr16:47296068
|
TTTTTA | T | 6 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0002t0002g0075others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1070+15167_1070+15 others(11): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47296068 | ||||||
| chr16:47296333
|
C | T | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.1070+14907G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47296333 | ||||||
| chr16:47296761
|
T | C | 4 | a0001c0002t0002g0077a0001c0002t0002g0086a0001c0002t0002g0087others(1): Show | 4 | HG00735.hp2 HG01074.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.1070+14479A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47296761 | ||||||
| chr16:47296790
|
G | A | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1070+14450C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47296790 | ||||||
| chr16:47296857
|
C | G | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1070+14383G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47296857 | ||||||
| chr16:47296865
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1070+14375G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47296865 | ||||||
| chr16:47296905
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005 | 3 | HG01891.hp2 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1070+14335A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47296905 | ||||||
| chr16:47297646
|
T | C | 8 | a0001c0001t0001g0007a0001c0001t0003g0068a0001c0001t0003g0069others(5): Show | 8 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1070+13594A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47297646 | ||||||
| chr16:47297743
|
T | C | 27 | a0001c0002t0001g0067a0001c0002t0001g0079a0001c0002t0001g0080others(24): Show | 27 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1070+13497A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47297743 | ||||||
| chr16:47298080
|
G | C | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.1070+13160C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47298080 | ||||||
| chr16:47298095
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1070+13145C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47298095 | ||||||
| chr16:47298299
|
A | T | 1 | a0001c0001t0001g0022 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1070+12941T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47298299 | ||||||
| chr16:47298793
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1070+12447A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47298793 | ||||||
| chr16:47299087
|
C | T | 38 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(35): Show | 38 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1070+12153G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47299087 | ||||||
| chr16:47299397
|
G | A | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1070+11843C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47299397 | ||||||
| chr16:47299433
|
TAGG | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(8): Show | 11 | HG00741.hp1 HG01169.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1070+11804_1070+11 others(9): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47299433 | ||||||
| chr16:47299434
|
AG | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0021others(3): Show | 6 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1070+11805delC | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47299434 | ||||||
| chr16:47299644
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1070+11596G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47299644 | ||||||
| chr16:47299712
|
C | A | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1070+11528G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47299712 | ||||||
| chr16:47299721
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1070+11519C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47299721 | ||||||
| chr16:47299734
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1070+11506G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47299734 | ||||||
| chr16:47299896
|
C | G | 1 | a0001c0002t0002g0087 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1070+11344G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47299896 | ||||||
| chr16:47300142
|
G | C | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1070+11098C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47300142 | ||||||
| chr16:47300234
|
A | G | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1070+11006T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47300234 | ||||||
| chr16:47300884
|
C | T | 1 | a0001c0002t0001g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1070+10356G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47300884 | ||||||
| chr16:47301135
|
T | C | 1 | a0001c0002t0002g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1070+10105A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47301135 | ||||||
| chr16:47301319
|
ACTGAGT | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1070+9915_1070+992 others(10): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47301319 | ||||||
| chr16:47301631
|
A | G | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1070+9609T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47301631 | ||||||
| chr16:47301686
|
G | A | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1070+9554C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47301686 | ||||||
| chr16:47302035
|
C | CA | 41 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1070+9204dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47302035 | ||||||
| chr16:47302380
|
AT | A | 8 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(5): Show | 8 | HG02280.hp1 HG02970.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1070+8859delA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47302380 | ||||||
| chr16:47302740
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1070+8500A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47302740 | ||||||
| chr16:47302766
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1070+8474T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47302766 | ||||||
| chr16:47302912
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG00741.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1070+8328C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47302912 | ||||||
| chr16:47303121
|
A | G | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1070+8119T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47303121 | ||||||
| chr16:47303281
|
G | T | 1 | a0001c0001t0001g0002 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1070+7959C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47303281 | ||||||
| chr16:47303379
|
G | T | 1 | a0001c0002t0002g0081 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1070+7861C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47303379 | ||||||
| chr16:47303404
|
C | A | 5 | a0001c0001t0001g0031a0001c0001t0001g0058a0001c0001t0001g0061others(2): Show | 5 | HG00642.hp2 HG02735.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1070+7836G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47303404 | ||||||
| chr16:47303495
|
AG | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1070+7744delC | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47303495 | ||||||
| chr16:47304309
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1070+6931C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47304309 | ||||||
| chr16:47305220
|
A | G | 34 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(31): Show | 34 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1070+6020T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47305220 | ||||||
| chr16:47306054
|
G | C | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1070+5186C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47306054 | ||||||
| chr16:47306592
|
T | G | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1070+4648A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47306592 | ||||||
| chr16:47306650
|
A | AT | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1070+4589dupA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47306650 | ||||||
| chr16:47306652
|
T | TA | 32 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(29): Show | 32 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1070+4587dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47306652 | ||||||
| chr16:47306804
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1070+4436C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47306804 | ||||||
| chr16:47307085
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1070+4155G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47307085 | ||||||
| chr16:47307093
|
C | CA | 15 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(12): Show | 15 | HG00280.hp2 HG01074.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1070+4146dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47307093 | ||||||
| chr16:47307093
|
C | CAA | 30 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(27): Show | 30 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1070+4145_1070+414 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47307093 | ||||||
| chr16:47307093
|
C | CAAA | 18 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(15): Show | 18 | HG00140.hp2 HG00741.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.1070+4144_1070+414 others(7): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47307093 | ||||||
| chr16:47307093
|
C | CAAAA | 6 | a0001c0001t0001g0016a0001c0001t0001g0043a0001c0001t0001g0047others(3): Show | 6 | HG01258.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1070+4143_1070+414 others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47307093 | ||||||
| chr16:47307093
|
C | CAAAAAAA others(4): Show |
5 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0094others(2): Show | 5 | HG01496.hp1 HG02258.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1070+4136_1070+414 others(15): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47307093 | ||||||
| chr16:47307093
|
C | CAAAAAAA others(5): Show |
13 | a0001c0002t0001g0079a0001c0002t0001g0096a0001c0002t0002g0072others(10): Show | 13 | HG01361.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1070+4135_1070+414 others(16): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47307093 | ||||||
| chr16:47307093
|
C | CAAAAAAA others(6): Show |
5 | a0001c0001t0001g0066a0001c0002t0002g0073a0001c0002t0002g0074others(2): Show | 5 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1070+4134_1070+414 others(17): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47307093 | ||||||
| chr16:47307093
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1070+4133_1070+414 others(18): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47307093 | ||||||
| chr16:47307093
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1070+4132_1070+414 others(19): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47307093 | ||||||
| chr16:47307093
|
C | CAAAAAAA others(11): Show |
2 | a0001c0002t0002g0087a0001c0002t0002g0089 | 2 | HG01074.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1070+4129_1070+414 others(22): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47307093 | ||||||
| chr16:47307093
|
C | CAAAAAAA others(12): Show |
1 | a0001c0002t0002g0086 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1070+4128_1070+414 others(23): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47307093 | ||||||
| chr16:47307093
|
C | CAAAAAAA others(13): Show |
1 | a0001c0002t0002g0088 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1070+4127_1070+414 others(24): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47307093 | ||||||
| chr16:47307093
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0023 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1070+4136_1070+414 others(15): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47307093 | ||||||
| chr16:47307116
|
A | AAAAAAAA others(5): Show |
1 | a0001c0002t0002g0084 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1070+4123_1070+412 others(16): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47307116 | ||||||
| chr16:47307290
|
A | G | 1 | a0001c0002t0002g0081 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1070+3950T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47307290 | ||||||
| chr16:47307353
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1070+3887C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47307353 | ||||||
| chr16:47308128
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1070+3112C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47308128 | ||||||
| chr16:47308595
|
G | A | 2 | a0001c0002t0001g0079a0001c0002t0001g0080 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1070+2645C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47308595 | ||||||
| chr16:47308649
|
T | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0050 | 2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1070+2591A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47308649 | ||||||
| chr16:47308812
|
G | C | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1070+2428C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47308812 | ||||||
| chr16:47308923
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1070+2317G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47308923 | ||||||
| chr16:47309107
|
C | T | 1 | a0001c0002t0002g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1070+2133G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47309107 | ||||||
| chr16:47309157
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1070+2083G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47309157 | ||||||
| chr16:47309954
|
A | G | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1070+1286T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47309954 | ||||||
| chr16:47310632
|
A | G | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1070+608T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47310632 | ||||||
| chr16:47311003
|
C | T | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1070+237G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47311003 | ||||||
| chr16:47311180
|
G | A | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1070+60C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 10/17 | chr16 | 47311180 | ||||||
| chr16:47311587
|
G | GA | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.898-176dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 9/17 | chr16 | 47311587 | ||||||
| chr16:47311709
|
A | C | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.898-297T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 9/17 | chr16 | 47311709 | ||||||
| chr16:47311764
|
T | C | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.898-352A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 9/17 | chr16 | 47311764 | ||||||
| chr16:47311904
|
CA | C | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.898-493delT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 9/17 | chr16 | 47311904 | ||||||
| chr16:47311997
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.898-585G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 9/17 | chr16 | 47311997 | ||||||
| chr16:47312033
|
G | A | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.898-621C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 9/17 | chr16 | 47312033 | ||||||
| chr16:47312132
|
T | C | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.898-720A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 9/17 | chr16 | 47312132 | ||||||
| chr16:47312506
|
GT | G | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.898-1095delA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 9/17 | chr16 | 47312506 | ||||||
| chr16:47312514
|
A | T | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.898-1102T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 9/17 | chr16 | 47312514 | ||||||
| chr16:47312718
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.897+1011A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 9/17 | chr16 | 47312718 | ||||||
| chr16:47312988
|
T | TA | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.897+740dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 9/17 | chr16 | 47312988 | ||||||
| chr16:47313177
|
G | A | 1 | a0001c0002t0001g0067 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.897+552C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 9/17 | chr16 | 47313177 | ||||||
| chr16:47313468
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.897+261G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 9/17 | chr16 | 47313468 | ||||||
| chr16:47313544
|
A | C | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.897+185T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 9/17 | chr16 | 47313544 | ||||||
| chr16:47313627
|
G | T | 1 | a0001c0001t0001g0020 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.897+102C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 9/17 | chr16 | 47313627 | ||||||
| chr16:47313869
|
G | A | 25 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(22): Show | 25 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.803-46C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47313869 | ||||||
| chr16:47314777
|
C | T | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.803-954G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47314777 | ||||||
| chr16:47314810
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.803-987G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47314810 | ||||||
| chr16:47315238
|
G | A | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.803-1415C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47315238 | ||||||
| chr16:47315768
|
C | CATATATA others(11): Show |
1 | a0001c0002t0002g0075 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.803-1946_803-1945i others(20): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47315768 | ||||||
| chr16:47315768
|
C | CATATATA others(13): Show |
14 | a0001c0002t0002g0072a0001c0002t0002g0074a0001c0002t0002g0076others(11): Show | 14 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.803-1946_803-1945i others(22): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47315768 | ||||||
| chr16:47315768
|
C | CATATATA others(15): Show |
3 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0002t0002g0073 | 3 | HG02723.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.803-1946_803-1945i others(24): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47315768 | ||||||
| chr16:47315768
|
C | CATATATA others(17): Show |
3 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0002g0077 | 3 | HG01361.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.803-1946_803-1945i others(26): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47315768 | ||||||
| chr16:47315768
|
C | CATATATA others(19): Show |
4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0002t0001g0094others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-1946_803-1945i others(28): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47315768 | ||||||
| chr16:47315768
|
C | CATATATA others(23): Show |
5 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0003g0068others(2): Show | 5 | HG01496.hp1 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-1946_803-1945i others(32): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47315768 | ||||||
| chr16:47315768
|
C | CATATATA others(27): Show |
1 | a0001c0002t0002g0082 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.803-1946_803-1945i others(36): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47315768 | ||||||
| chr16:47315768
|
C | CATATATA others(29): Show |
2 | a0001c0002t0002g0083a0001c0002t0002g0084 | 2 | HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.803-1946_803-1945i others(38): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47315768 | ||||||
| chr16:47315770
|
T | TATATATA others(13): Show |
2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.803-1948_803-1947i others(22): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47315770 | ||||||
| chr16:47315775
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.803-1953_803-1952i others(24): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47315775 | ||||||
| chr16:47315775
|
A | ATATATAT others(9): Show |
4 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0091others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-1953_803-1952i others(18): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47315775 | ||||||
| chr16:47316263
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.803-2440A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47316263 | ||||||
| chr16:47316265
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.803-2442T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47316265 | ||||||
| chr16:47316384
|
A | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.803-2561T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47316384 | ||||||
| chr16:47316547
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.803-2724G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47316547 | ||||||
| chr16:47316740
|
T | A | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.803-2917A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47316740 | ||||||
| chr16:47316781
|
A | C | 1 | a0001c0002t0002g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.803-2958T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47316781 | ||||||
| chr16:47316801
|
C | T | 4 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0091others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-2978G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47316801 | ||||||
| chr16:47317275
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.803-3452A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47317275 | ||||||
| chr16:47317676
|
G | A | 39 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(36): Show | 39 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.803-3853C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47317676 | ||||||
| chr16:47317732
|
C | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(24): Show | 27 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.803-3909G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47317732 | ||||||
| chr16:47317921
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.803-4098C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47317921 | ||||||
| chr16:47318101
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.803-4278C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47318101 | ||||||
| chr16:47318971
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.803-5148G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47318971 | ||||||
| chr16:47319141
|
G | T | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.803-5318C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47319141 | ||||||
| chr16:47319260
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.803-5437A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47319260 | ||||||
| chr16:47319580
|
T | A | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.803-5757A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47319580 | ||||||
| chr16:47319582
|
T | C | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-5759A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47319582 | ||||||
| chr16:47319962
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.803-6139G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47319962 | ||||||
| chr16:47320758
|
A | C | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.803-6935T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47320758 | ||||||
| chr16:47320810
|
G | C | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.803-6987C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47320810 | ||||||
| chr16:47321068
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.803-7245A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47321068 | ||||||
| chr16:47321095
|
G | C | 1 | a0001c0001t0001g0017 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.803-7272C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47321095 | ||||||
| chr16:47321500
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0052 | 2 | HG00140.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.803-7677C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47321500 | ||||||
| chr16:47321954
|
T | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.803-8131A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47321954 | ||||||
| chr16:47322021
|
T | C | 22 | a0001c0002t0001g0094a0001c0002t0002g0072a0001c0002t0002g0073others(19): Show | 22 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.803-8198A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47322021 | ||||||
| chr16:47322257
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.803-8434G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47322257 | ||||||
| chr16:47322985
|
T | TTTTA | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.803-9163_803-9162i others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47322985 | ||||||
| chr16:47323461
|
GTATTATC others(9): Show |
G | 3 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0004t0001g0071 | 3 | HG02622.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.803-9654_803-9639d others(18): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47323461 | ||||||
| chr16:47323640
|
G | A | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.803-9817C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47323640 | ||||||
| chr16:47323651
|
C | CAA | 38 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(35): Show | 38 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.803-9829_803-9828i others(4): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47323651 | ||||||
| chr16:47323652
|
A | AAG | 4 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0091others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-9830_803-9829i others(4): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47323652 | ||||||
| chr16:47323727
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.803-9904A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47323727 | ||||||
| chr16:47323728
|
A | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.803-9905T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47323728 | ||||||
| chr16:47323855
|
A | C | 1 | a0001c0001t0001g0023 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.803-10032T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47323855 | ||||||
| chr16:47324111
|
C | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.803-10288G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47324111 | ||||||
| chr16:47324172
|
G | A | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.803-10349C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47324172 | ||||||
| chr16:47324270
|
C | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.803-10447G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47324270 | ||||||
| chr16:47324433
|
A | G | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.803-10610T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47324433 | ||||||
| chr16:47324448
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.803-10625G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47324448 | ||||||
| chr16:47324509
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.803-10686C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47324509 | ||||||
| chr16:47324510
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.803-10687A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47324510 | ||||||
| chr16:47324530
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.803-10707C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47324530 | ||||||
| chr16:47324534
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.803-10711C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47324534 | ||||||
| chr16:47324910
|
C | T | 16 | a0001c0002t0002g0072a0001c0002t0002g0073a0001c0002t0002g0074others(13): Show | 16 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.803-11087G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47324910 | ||||||
| chr16:47324926
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.803-11103C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47324926 | ||||||
| chr16:47324933
|
A | G | 4 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0091others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-11110T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47324933 | ||||||
| chr16:47325057
|
T | C | 6 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.803-11234A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47325057 | ||||||
| chr16:47325237
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.803-11414G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47325237 | ||||||
| chr16:47325324
|
A | C | 41 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.803-11501T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47325324 | ||||||
| chr16:47325419
|
A | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.803-11596T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47325419 | ||||||
| chr16:47325473
|
C | A | 1 | a0001c0001t0001g0020 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.803-11650G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47325473 | ||||||
| chr16:47325593
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.803-11770C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47325593 | ||||||
| chr16:47325712
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.803-11889A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47325712 | ||||||
| chr16:47326075
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.803-12252T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47326075 | ||||||
| chr16:47326092
|
C | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0099 | 2 | HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.803-12269G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47326092 | ||||||
| chr16:47326245
|
C | T | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.803-12422G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47326245 | ||||||
| chr16:47326460
|
G | T | 1 | a0001c0001t0003g0070 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.803-12637C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47326460 | ||||||
| chr16:47326480
|
T | C | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.803-12657A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47326480 | ||||||
| chr16:47326600
|
T | C | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.803-12777A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47326600 | ||||||
| chr16:47326687
|
A | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0051 | 2 | HG00642.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.803-12864T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47326687 | ||||||
| chr16:47326985
|
A | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.803-13162T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47326985 | ||||||
| chr16:47327563
|
T | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.803-13740A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47327563 | ||||||
| chr16:47327745
|
T | C | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-13922A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47327745 | ||||||
| chr16:47327878
|
C | G | 1 | a0001c0001t0001g0031 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.803-14055G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47327878 | ||||||
| chr16:47328022
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.803-14199C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47328022 | ||||||
| chr16:47328415
|
T | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0038others(3): Show | 6 | HG02055.hp2 HG02559.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.803-14592A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47328415 | ||||||
| chr16:47328492
|
A | T | 1 | a0001c0002t0002g0084 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.803-14669T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47328492 | ||||||
| chr16:47328960
|
C | A | 2 | a0001c0002t0001g0079a0001c0002t0001g0080 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.803-15137G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47328960 | ||||||
| chr16:47329012
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.803-15189G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47329012 | ||||||
| chr16:47329195
|
C | G | 1 | a0001c0001t0001g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.803-15372G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47329195 | ||||||
| chr16:47329290
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.803-15467G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47329290 | ||||||
| chr16:47329328
|
A | G | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-15505T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47329328 | ||||||
| chr16:47329490
|
C | T | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.803-15667G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47329490 | ||||||
| chr16:47329655
|
G | A | 3 | a0001c0002t0004g0064a0001c0002t0004g0065a0001c0002t0004g0095 | 3 | HG02895.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.803-15832C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47329655 | ||||||
| chr16:47329713
|
C | G | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.803-15890G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47329713 | ||||||
| chr16:47329973
|
T | G | 1 | a0001c0001t0001g0022 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.803-16150A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47329973 | ||||||
| chr16:47330705
|
C | G | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-16882G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47330705 | ||||||
| chr16:47330787
|
A | C | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-16964T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47330787 | ||||||
| chr16:47331634
|
T | C | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.803-17811A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47331634 | ||||||
| chr16:47331640
|
T | A | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.803-17817A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47331640 | ||||||
| chr16:47331999
|
C | T | 3 | a0001c0002t0002g0082a0001c0002t0002g0083a0001c0002t0002g0084 | 3 | HG02257.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.803-18176G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47331999 | ||||||
| chr16:47332073
|
G | T | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.803-18250C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47332073 | ||||||
| chr16:47332196
|
TAATAAAA others(3): Show |
T | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-18383_803-1837 others(14): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47332196 | ||||||
| chr16:47332425
|
C | T | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.803-18602G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47332425 | ||||||
| chr16:47332626
|
A | G | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-18803T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47332626 | ||||||
| chr16:47333168
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.803-19345C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47333168 | ||||||
| chr16:47333247
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.803-19424C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47333247 | ||||||
| chr16:47333284
|
A | C | 1 | a0001c0001t0001g0054 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.803-19461T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47333284 | ||||||
| chr16:47333360
|
T | G | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.803-19537A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47333360 | ||||||
| chr16:47334104
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.803-20281T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47334104 | ||||||
| chr16:47334957
|
G | C | 1 | a0001c0002t0002g0084 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.803-21134C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47334957 | ||||||
| chr16:47335240
|
C | T | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.803-21417G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47335240 | ||||||
| chr16:47335241
|
C | T | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.803-21418G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47335241 | ||||||
| chr16:47335243
|
G | T | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-21420C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47335243 | ||||||
| chr16:47335936
|
G | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0058 | 2 | HG02735.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.803-22113C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47335936 | ||||||
| chr16:47336019
|
C | T | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.803-22196G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47336019 | ||||||
| chr16:47336273
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.803-22450G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47336273 | ||||||
| chr16:47336685
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.803-22862G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47336685 | ||||||
| chr16:47336720
|
T | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.803-22897A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47336720 | ||||||
| chr16:47336987
|
A | T | 1 | a0001c0001t0001g0022 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.803-23164T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47336987 | ||||||
| chr16:47337137
|
C | CA | 29 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(26): Show | 29 | HG00280.hp1 HG00609.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.803-23315dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47337137 | ||||||
| chr16:47337188
|
T | C | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.803-23365A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47337188 | ||||||
| chr16:47337359
|
C | T | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-23536G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47337359 | ||||||
| chr16:47337752
|
C | T | 2 | a0001c0002t0002g0073a0001c0002t0002g0074 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.803-23929G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47337752 | ||||||
| chr16:47337854
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.803-24031A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47337854 | ||||||
| chr16:47338240
|
T | C | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.803-24417A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47338240 | ||||||
| chr16:47338283
|
C | T | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.803-24460G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47338283 | ||||||
| chr16:47338388
|
T | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.803-24565A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47338388 | ||||||
| chr16:47338670
|
A | T | 46 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(43): Show | 46 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.803-24847T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47338670 | ||||||
| chr16:47339209
|
G | A | 1 | a0001c0002t0001g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.803-25386C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47339209 | ||||||
| chr16:47339226
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.803-25403G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47339226 | ||||||
| chr16:47339333
|
T | C | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-25510A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47339333 | ||||||
| chr16:47339690
|
C | A | 1 | a0001c0002t0001g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.803-25867G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47339690 | ||||||
| chr16:47339733
|
T | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.803-25910A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47339733 | ||||||
| chr16:47339977
|
C | T | 3 | a0001c0002t0002g0086a0001c0002t0002g0087a0001c0002t0002g0088 | 3 | HG00735.hp2 HG01074.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.802+25811G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47339977 | ||||||
| chr16:47340053
|
TGTATTTA others(5): Show |
T | 1 | a0001c0001t0001g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.802+25723_802+2573 others(16): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47340053 | ||||||
| chr16:47340066
|
C | A | 1 | a0001c0001t0001g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.802+25722G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47340066 | ||||||
| chr16:47340204
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.802+25584G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47340204 | ||||||
| chr16:47340939
|
C | T | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.802+24849G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47340939 | ||||||
| chr16:47341249
|
T | C | 5 | a0001c0001t0001g0031a0001c0001t0001g0058a0001c0001t0001g0061others(2): Show | 5 | HG00642.hp2 HG02735.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.802+24539A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47341249 | ||||||
| chr16:47341256
|
A | AAAATAAA others(1): Show |
7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+24524_802+2453 others(12): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47341256 | ||||||
| chr16:47341415
|
A | G | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.802+24373T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47341415 | ||||||
| chr16:47342291
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.802+23497T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47342291 | ||||||
| chr16:47342705
|
T | C | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.802+23083A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47342705 | ||||||
| chr16:47342894
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.802+22894T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47342894 | ||||||
| chr16:47343147
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.802+22641A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47343147 | ||||||
| chr16:47343576
|
T | A | 1 | a0001c0004t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.802+22212A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47343576 | ||||||
| chr16:47343649
|
G | A | 3 | a0001c0002t0002g0086a0001c0002t0002g0087a0001c0002t0002g0088 | 3 | HG00735.hp2 HG01074.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.802+22139C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47343649 | ||||||
| chr16:47343740
|
C | T | 2 | a0001c0002t0002g0075a0001c0002t0002g0076 | 2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.802+22048G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47343740 | ||||||
| chr16:47344432
|
T | C | 1 | a0001c0002t0001g0080 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.802+21356A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47344432 | ||||||
| chr16:47344830
|
C | T | 20 | a0001c0002t0001g0094a0001c0002t0002g0072a0001c0002t0002g0073others(17): Show | 20 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.802+20958G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47344830 | ||||||
| chr16:47344954
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.802+20834A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47344954 | ||||||
| chr16:47345036
|
G | A | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.802+20752C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47345036 | ||||||
| chr16:47345109
|
T | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.802+20679A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47345109 | ||||||
| chr16:47345287
|
A | C | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.802+20501T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47345287 | ||||||
| chr16:47345291
|
CT | C | 35 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(32): Show | 35 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.802+20496delA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47345291 | ||||||
| chr16:47345302
|
T | G | 1 | a0001c0001t0001g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.802+20486A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47345302 | ||||||
| chr16:47345302
|
TG | T | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+20485delC | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47345302 | ||||||
| chr16:47345303
|
G | T | 27 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(24): Show | 27 | HG00140.hp1 HG00280.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.802+20485C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47345303 | ||||||
| chr16:47345340
|
G | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG00735.hp1 HG01169.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.802+20448C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47345340 | ||||||
| chr16:47345457
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.802+20331G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47345457 | ||||||
| chr16:47345542
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.802+20246C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47345542 | ||||||
| chr16:47345813
|
A | T | 1 | a0001c0001t0001g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.802+19975T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47345813 | ||||||
| chr16:47345815
|
G | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.802+19973C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47345815 | ||||||
| chr16:47347250
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.802+18538C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47347250 | ||||||
| chr16:47347354
|
C | T | 1 | a0001c0002t0002g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.802+18434G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47347354 | ||||||
| chr16:47347406
|
A | G | 1 | a0001c0001t0001g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.802+18382T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47347406 | ||||||
| chr16:47347424
|
C | T | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+18364G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47347424 | ||||||
| chr16:47347846
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.802+17942G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47347846 | ||||||
| chr16:47347944
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.802+17844G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47347944 | ||||||
| chr16:47347948
|
T | C | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.802+17840A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47347948 | ||||||
| chr16:47348059
|
G | A | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.802+17729C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47348059 | ||||||
| chr16:47348409
|
A | G | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.802+17379T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47348409 | ||||||
| chr16:47348416
|
T | C | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.802+17372A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47348416 | ||||||
| chr16:47348501
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.802+17287C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47348501 | ||||||
| chr16:47348759
|
T | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.802+17029A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47348759 | ||||||
| chr16:47348842
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.802+16946A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47348842 | ||||||
| chr16:47348968
|
C | T | 4 | a0001c0002t0001g0094a0001c0002t0002g0082a0001c0002t0002g0083others(1): Show | 4 | HG02257.hp2 HG02922.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+16820G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47348968 | ||||||
| chr16:47348991
|
T | A | 1 | a0001c0001t0001g0006 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.802+16797A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47348991 | ||||||
| chr16:47349119
|
A | C | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+16669T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47349119 | ||||||
| chr16:47349132
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.802+16656G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47349132 | ||||||
| chr16:47349176
|
C | T | 2 | a0001c0002t0001g0079a0001c0002t0001g0080 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.802+16612G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47349176 | ||||||
| chr16:47349236
|
A | C | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.802+16552T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47349236 | ||||||
| chr16:47349335
|
CAT | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.802+16451_802+1645 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47349335 | ||||||
| chr16:47349343
|
C | A | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.802+16445G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47349343 | ||||||
| chr16:47349375
|
C | A | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.802+16413G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47349375 | ||||||
| chr16:47349529
|
A | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.802+16259T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47349529 | ||||||
| chr16:47349911
|
C | G | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.802+15877G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47349911 | ||||||
| chr16:47350066
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.802+15722A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47350066 | ||||||
| chr16:47350138
|
T | C | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.802+15650A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47350138 | ||||||
| chr16:47350302
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.802+15486A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47350302 | ||||||
| chr16:47350497
|
TC | T | 4 | a0001c0002t0001g0094a0001c0002t0002g0082a0001c0002t0002g0083others(1): Show | 4 | HG02257.hp2 HG02922.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+15290delG | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47350497 | ||||||
| chr16:47350510
|
C | G | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.802+15278G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47350510 | ||||||
| chr16:47350643
|
G | A | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+15145C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47350643 | ||||||
| chr16:47350652
|
C | A | 1 | a0001c0001t0001g0053 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.802+15136G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47350652 | ||||||
| chr16:47351053
|
A | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.802+14735T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47351053 | ||||||
| chr16:47351299
|
C | T | 1 | a0001c0003t0001g0001 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.802+14489G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47351299 | ||||||
| chr16:47351373
|
G | C | 8 | a0001c0001t0001g0042a0001c0001t0003g0068a0001c0001t0003g0069others(5): Show | 8 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.802+14415C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47351373 | ||||||
| chr16:47351731
|
CA | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.802+14056delT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47351731 | ||||||
| chr16:47351942
|
CA | C | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.802+13845delT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47351942 | ||||||
| chr16:47352213
|
G | C | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.802+13575C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47352213 | ||||||
| chr16:47352453
|
A | G | 3 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0004t0001g0071 | 3 | HG02622.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.802+13335T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47352453 | ||||||
| chr16:47352666
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.802+13122A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47352666 | ||||||
| chr16:47352708
|
G | C | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.802+13080C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47352708 | ||||||
| chr16:47352909
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.802+12879G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47352909 | ||||||
| chr16:47353018
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.802+12770A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47353018 | ||||||
| chr16:47353072
|
G | C | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+12716C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47353072 | ||||||
| chr16:47353139
|
A | T | 1 | a0001c0001t0001g0054 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.802+12649T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47353139 | ||||||
| chr16:47353211
|
A | T | 6 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0091others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+12577T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47353211 | ||||||
| chr16:47353273
|
G | A | 1 | a0001c0002t0002g0087 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.802+12515C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47353273 | ||||||
| chr16:47353273
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.802+12515C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47353273 | ||||||
| chr16:47353303
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.802+12485A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47353303 | ||||||
| chr16:47353420
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.802+12368A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47353420 | ||||||
| chr16:47353459
|
T | C | 1 | a0001c0004t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.802+12329A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47353459 | ||||||
| chr16:47353728
|
T | C | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.802+12060A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47353728 | ||||||
| chr16:47353838
|
A | C | 1 | a0001c0001t0001g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.802+11950T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47353838 | ||||||
| chr16:47354141
|
T | C | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.802+11647A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47354141 | ||||||
| chr16:47354177
|
A | G | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.802+11611T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47354177 | ||||||
| chr16:47354268
|
C | A | 31 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(28): Show | 31 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.802+11520G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47354268 | ||||||
| chr16:47354973
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.802+10815G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47354973 | ||||||
| chr16:47354987
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.802+10801G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47354987 | ||||||
| chr16:47355205
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.802+10583G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47355205 | ||||||
| chr16:47355461
|
A | C | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.802+10327T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47355461 | ||||||
| chr16:47355650
|
T | C | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.802+10138A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47355650 | ||||||
| chr16:47355851
|
TG | T | 35 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(32): Show | 35 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.802+9936delC | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47355851 | ||||||
| chr16:47356211
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.802+9577C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47356211 | ||||||
| chr16:47356528
|
T | C | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.802+9260A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47356528 | ||||||
| chr16:47356689
|
C | G | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.802+9099G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47356689 | ||||||
| chr16:47356815
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.802+8973T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47356815 | ||||||
| chr16:47357158
|
A | G | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.802+8630T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47357158 | ||||||
| chr16:47357390
|
G | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0063 | 2 | HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.802+8398C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47357390 | ||||||
| chr16:47357438
|
C | A | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.802+8350G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47357438 | ||||||
| chr16:47357503
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.802+8285C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47357503 | ||||||
| chr16:47357508
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.802+8280C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47357508 | ||||||
| chr16:47357614
|
C | CA | 24 | a0001c0001t0001g0017a0001c0002t0001g0079a0001c0002t0001g0080others(21): Show | 24 | HG00280.hp1 HG00735.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.802+8173dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47357614 | ||||||
| chr16:47358698
|
T | C | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.802+7090A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47358698 | ||||||
| chr16:47358875
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.802+6913C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47358875 | ||||||
| chr16:47358990
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.802+6798T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47358990 | ||||||
| chr16:47359253
|
ACT | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.802+6533_802+6534d others(4): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47359253 | ||||||
| chr16:47359688
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0054 | 3 | HG00280.hp2 HG00609.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.802+6100G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47359688 | ||||||
| chr16:47359852
|
T | C | 4 | a0001c0002t0001g0094a0001c0002t0002g0082a0001c0002t0002g0083others(1): Show | 4 | HG02257.hp2 HG02922.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+5936A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47359852 | ||||||
| chr16:47360209
|
A | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.802+5579T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47360209 | ||||||
| chr16:47361240
|
A | G | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.802+4548T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47361240 | ||||||
| chr16:47361475
|
C | T | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.802+4313G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47361475 | ||||||
| chr16:47361640
|
C | A | 1 | a0001c0001t0001g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.802+4148G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47361640 | ||||||
| chr16:47361799
|
A | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.802+3989T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47361799 | ||||||
| chr16:47362055
|
C | T | 6 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0038others(3): Show | 6 | HG02055.hp2 HG02559.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.802+3733G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47362055 | ||||||
| chr16:47362437
|
C | G | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+3351G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47362437 | ||||||
| chr16:47362888
|
C | CTTAT | 4 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0091others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+2896_802+2899d others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47362888 | ||||||
| chr16:47362978
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG00741.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.802+2810G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47362978 | ||||||
| chr16:47363007
|
C | A | 4 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0091others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+2781G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47363007 | ||||||
| chr16:47363211
|
AAAGAC | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.802+2572_802+2576d others(7): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47363211 | ||||||
| chr16:47363870
|
C | A | 1 | a0001c0003t0001g0001 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.802+1918G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47363870 | ||||||
| chr16:47364203
|
A | G | 1 | a0001c0002t0001g0067 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.802+1585T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47364203 | ||||||
| chr16:47364326
|
T | C | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG00735.hp1 HG01169.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.802+1462A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47364326 | ||||||
| chr16:47365000
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.802+788G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47365000 | ||||||
| chr16:47365040
|
T | G | 1 | a0001c0001t0001g0043 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.802+748A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47365040 | ||||||
| chr16:47365093
|
G | C | 5 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040others(2): Show | 5 | HG02559.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.802+695C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47365093 | ||||||
| chr16:47365397
|
T | TA | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.802+390dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47365397 | ||||||
| chr16:47365549
|
T | C | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.802+239A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47365549 | ||||||
| chr16:47365759
|
C | CT | 7 | a0001c0001t0001g0066a0001c0001t0001g0107a0001c0001t0001g0108others(4): Show | 7 | HG00735.hp1 HG01169.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+28dupA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 8/17 | chr16 | 47365759 | ||||||
| chr16:47366236
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.721-367T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47366236 | ||||||
| chr16:47366558
|
C | G | 1 | a0001c0001t0001g0017 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.721-689G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47366558 | ||||||
| chr16:47366952
|
T | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.721-1083A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47366952 | ||||||
| chr16:47366976
|
G | A | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.721-1107C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47366976 | ||||||
| chr16:47367118
|
AT | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG00741.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.721-1250delA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47367118 | ||||||
| chr16:47367376
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.721-1507C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47367376 | ||||||
| chr16:47367549
|
G | A | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.721-1680C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47367549 | ||||||
| chr16:47367885
|
G | C | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.721-2016C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47367885 | ||||||
| chr16:47367894
|
T | C | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.721-2025A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47367894 | ||||||
| chr16:47368237
|
T | TA | 29 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(26): Show | 29 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.721-2369dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47368237 | ||||||
| chr16:47368453
|
G | T | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.721-2584C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47368453 | ||||||
| chr16:47368491
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.721-2622G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47368491 | ||||||
| chr16:47368537
|
C | T | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.721-2668G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47368537 | ||||||
| chr16:47368555
|
C | CA | 5 | a0001c0001t0001g0022a0001c0001t0001g0051a0001c0001t0001g0066others(2): Show | 5 | HG00741.hp2 HG01496.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.721-2687dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47368555 | ||||||
| chr16:47368555
|
C | CAAAAA | 13 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.721-2691_721-2687d others(7): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47368555 | ||||||
| chr16:47368555
|
C | CAAAAAA | 11 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0098others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.721-2692_721-2687d others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47368555 | ||||||
| chr16:47368555
|
C | CAAAAAAA others(1): Show |
4 | a0001c0002t0002g0077a0001c0002t0002g0078a0001c0002t0002g0081others(1): Show | 4 | HG01109.hp2 HG01255.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-2694_721-2687d others(10): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47368555 | ||||||
| chr16:47368555
|
CA | C | 42 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(39): Show | 42 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.721-2687delT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47368555 | ||||||
| chr16:47368555
|
CAA | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0050others(1): Show | 4 | HG02897.hp2 HG03540.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-2688_721-2687d others(4): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47368555 | ||||||
| chr16:47369160
|
C | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0104a0001c0001t0001g0105others(1): Show | 4 | HG02280.hp1 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-3291G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47369160 | ||||||
| chr16:47369399
|
G | C | 1 | a0001c0001t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.721-3530C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47369399 | ||||||
| chr16:47369833
|
C | CT | 10 | a0001c0001t0001g0066a0001c0001t0003g0069a0001c0001t0003g0070others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.721-3965dupA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47369833 | ||||||
| chr16:47369833
|
C | CTT | 22 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0003g0068others(19): Show | 22 | HG01109.hp2 HG01361.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.721-3966_721-3965d others(4): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47369833 | ||||||
| chr16:47369833
|
C | CTTT | 9 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0106others(6): Show | 9 | HG00735.hp2 HG01074.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.721-3967_721-3965d others(5): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47369833 | ||||||
| chr16:47369833
|
CT | C | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(57): Show | 60 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.721-3965delA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47369833 | ||||||
| chr16:47369833
|
CTT | C | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0035others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-3966_721-3965d others(4): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47369833 | ||||||
| chr16:47370266
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.721-4397C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47370266 | ||||||
| chr16:47370426
|
T | A | 1 | a0001c0001t0001g0007 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.721-4557A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47370426 | ||||||
| chr16:47370597
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0099 | 2 | HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.721-4728G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47370597 | ||||||
| chr16:47370664
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.721-4795G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47370664 | ||||||
| chr16:47370742
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.721-4873C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47370742 | ||||||
| chr16:47370781
|
G | A | 2 | a0001c0002t0004g0064a0001c0002t0004g0065 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.721-4912C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47370781 | ||||||
| chr16:47370843
|
C | T | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.721-4974G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47370843 | ||||||
| chr16:47371223
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.720+4653G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47371223 | ||||||
| chr16:47371677
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.720+4199A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47371677 | ||||||
| chr16:47371729
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.720+4147C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47371729 | ||||||
| chr16:47371913
|
CT | C | 23 | a0001c0002t0001g0094a0001c0002t0002g0072a0001c0002t0002g0073others(20): Show | 23 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.720+3962delA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47371913 | ||||||
| chr16:47371945
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.720+3931C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47371945 | ||||||
| chr16:47372053
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.720+3823G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47372053 | ||||||
| chr16:47372061
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.720+3815G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47372061 | ||||||
| chr16:47372113
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.720+3763C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47372113 | ||||||
| chr16:47372249
|
A | C | 1 | a0001c0001t0001g0017 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.720+3627T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47372249 | ||||||
| chr16:47372455
|
C | CT | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+3420dupA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47372455 | ||||||
| chr16:47373431
|
A | G | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.720+2445T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47373431 | ||||||
| chr16:47373720
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.720+2156G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47373720 | ||||||
| chr16:47374300
|
C | A | 2 | a0001c0002t0001g0079a0001c0002t0001g0080 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.720+1576G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47374300 | ||||||
| chr16:47374350
|
C | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.720+1526G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47374350 | ||||||
| chr16:47374636
|
C | T | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.720+1240G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47374636 | ||||||
| chr16:47374823
|
T | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.720+1053A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47374823 | ||||||
| chr16:47375002
|
T | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.720+874A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47375002 | ||||||
| chr16:47375243
|
G | C | 1 | a0001c0002t0002g0078 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.720+633C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47375243 | ||||||
| chr16:47375821
|
T | A | 1 | a0001c0001t0001g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.720+55A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 7/17 | chr16 | 47375821 | ||||||
| chr16:47376036
|
C | T | 40 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(37): Show | 40 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.656-96G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47376036 | ||||||
| chr16:47376195
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.656-255C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47376195 | ||||||
| chr16:47376530
|
C | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.656-590G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47376530 | ||||||
| chr16:47376640
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.656-700G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47376640 | ||||||
| chr16:47376713
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.656-773G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47376713 | ||||||
| chr16:47376736
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.656-796C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47376736 | ||||||
| chr16:47376736
|
G | C | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.656-796C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47376736 | ||||||
| chr16:47376800
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.656-860G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47376800 | ||||||
| chr16:47376961
|
C | CA | 8 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0030others(5): Show | 8 | HG01258.hp2 HG02055.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.656-1022_656-1021i others(3): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47376961 | ||||||
| chr16:47376962
|
C | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(98): Show | 101 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.656-1022G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47376962 | ||||||
| chr16:47376964
|
C | A | 8 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0030others(5): Show | 8 | HG01258.hp2 HG02055.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.656-1024G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47376964 | ||||||
| chr16:47376964
|
C | CAA | 17 | a0001c0001t0001g0005a0001c0002t0001g0080a0001c0002t0001g0094others(14): Show | 17 | HG00735.hp2 HG01074.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.656-1026_656-1025d others(4): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47376964 | ||||||
| chr16:47376964
|
C | CAAA | 11 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0097others(8): Show | 11 | HG01109.hp2 HG01361.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.656-1027_656-1025d others(5): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47376964 | ||||||
| chr16:47376964
|
C | CAAAA | 5 | a0001c0001t0003g0070a0001c0001t0003g0091a0001c0001t0003g0092others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.656-1028_656-1025d others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47376964 | ||||||
| chr16:47376964
|
C | CAAAAAAA others(9): Show |
1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.656-1040_656-1025d others(18): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47376964 | ||||||
| chr16:47376964
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.656-1046_656-1025d others(24): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47376964 | ||||||
| chr16:47376964
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0100 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.656-1047_656-1025d others(25): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47376964 | ||||||
| chr16:47376964
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.656-1049_656-1025d others(27): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47376964 | ||||||
| chr16:47376980
|
A | AAAAAAAA others(9): Show |
1 | a0001c0002t0001g0067 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.656-1041_656-1040i others(18): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47376980 | ||||||
| chr16:47376980
|
A | AAAAAAAA others(8): Show |
1 | a0001c0002t0001g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.656-1041_656-1040i others(17): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47376980 | ||||||
| chr16:47377042
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.656-1102G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47377042 | ||||||
| chr16:47377292
|
T | C | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG00140.hp1 HG00280.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.656-1352A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47377292 | ||||||
| chr16:47377423
|
A | T | 1 | a0001c0001t0001g0034 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.656-1483T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47377423 | ||||||
| chr16:47377565
|
G | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG00741.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.656-1625C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47377565 | ||||||
| chr16:47377672
|
T | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.656-1732A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47377672 | ||||||
| chr16:47378186
|
T | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.656-2246A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47378186 | ||||||
| chr16:47378444
|
C | T | 4 | a0001c0002t0002g0075a0001c0002t0002g0076a0001c0002t0002g0085others(1): Show | 4 | HG01891.hp1 HG02258.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-2504G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47378444 | ||||||
| chr16:47378453
|
A | G | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.656-2513T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47378453 | ||||||
| chr16:47378670
|
T | C | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.656-2730A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47378670 | ||||||
| chr16:47378874
|
T | C | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.656-2934A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47378874 | ||||||
| chr16:47379304
|
G | A | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-3364C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47379304 | ||||||
| chr16:47379688
|
C | CA | 4 | a0001c0001t0001g0054a0001c0001t0001g0104a0001c0001t0001g0105others(1): Show | 4 | HG00609.hp2 HG02280.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-3749dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47379688 | ||||||
| chr16:47380048
|
C | CA | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0100others(5): Show | 8 | HG01496.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.656-4109dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47380048 | ||||||
| chr16:47380048
|
C | CAA | 4 | a0001c0001t0001g0066a0001c0001t0001g0104a0001c0001t0001g0105others(1): Show | 4 | HG02280.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-4110_656-4109d others(4): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47380048 | ||||||
| chr16:47380048
|
C | CAAA | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-4111_656-4109d others(5): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47380048 | ||||||
| chr16:47380284
|
T | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.656-4344A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47380284 | ||||||
| chr16:47380691
|
C | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.656-4751G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47380691 | ||||||
| chr16:47380827
|
G | A | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.656-4887C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47380827 | ||||||
| chr16:47381183
|
T | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.656-5243A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47381183 | ||||||
| chr16:47381327
|
T | C | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.656-5387A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47381327 | ||||||
| chr16:47382017
|
A | T | 5 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040others(2): Show | 5 | HG02559.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.656-6077T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47382017 | ||||||
| chr16:47382203
|
G | A | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-6263C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47382203 | ||||||
| chr16:47382520
|
A | G | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.656-6580T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47382520 | ||||||
| chr16:47382528
|
T | A | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-6588A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47382528 | ||||||
| chr16:47382603
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0058 | 2 | HG02735.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.656-6663G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47382603 | ||||||
| chr16:47382649
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005 | 3 | HG01891.hp2 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.656-6709G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47382649 | ||||||
| chr16:47383339
|
T | A | 1 | a0001c0001t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.656-7399A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47383339 | ||||||
| chr16:47383341
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.656-7401T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47383341 | ||||||
| chr16:47383542
|
C | T | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.656-7602G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47383542 | ||||||
| chr16:47383829
|
A | G | 34 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(31): Show | 34 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.656-7889T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47383829 | ||||||
| chr16:47383869
|
A | C | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.656-7929T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47383869 | ||||||
| chr16:47383957
|
C | A | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.656-8017G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47383957 | ||||||
| chr16:47384520
|
G | A | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.656-8580C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47384520 | ||||||
| chr16:47384870
|
G | A | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.656-8930C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47384870 | ||||||
| chr16:47384876
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.656-8936C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47384876 | ||||||
| chr16:47385045
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.656-9105C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47385045 | ||||||
| chr16:47385257
|
T | C | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-9317A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47385257 | ||||||
| chr16:47385262
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.656-9322G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47385262 | ||||||
| chr16:47386538
|
T | G | 1 | a0001c0004t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.656-10598A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47386538 | ||||||
| chr16:47387304
|
A | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.656-11364T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47387304 | ||||||
| chr16:47387315
|
A | G | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG00735.hp1 HG01169.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.656-11375T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47387315 | ||||||
| chr16:47387347
|
C | A | 6 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0091others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-11407G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47387347 | ||||||
| chr16:47387737
|
G | A | 1 | a0001c0002t0001g0067 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.656-11797C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47387737 | ||||||
| chr16:47388006
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.656-12066G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47388006 | ||||||
| chr16:47388193
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.656-12253C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47388193 | ||||||
| chr16:47388767
|
G | T | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.656-12827C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47388767 | ||||||
| chr16:47388775
|
T | C | 2 | a0001c0002t0001g0079a0001c0002t0001g0080 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.656-12835A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47388775 | ||||||
| chr16:47388911
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.656-12971C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47388911 | ||||||
| chr16:47389529
|
T | C | 45 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(42): Show | 45 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.656-13589A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47389529 | ||||||
| chr16:47390620
|
C | T | 1 | a0001c0002t0002g0085 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.656-14680G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47390620 | ||||||
| chr16:47390711
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.656-14771G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47390711 | ||||||
| chr16:47390917
|
T | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(15): Show | 18 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.656-14977A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47390917 | ||||||
| chr16:47391045
|
T | C | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.656-15105A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47391045 | ||||||
| chr16:47391646
|
G | T | 1 | a0001c0001t0001g0018 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.656-15706C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47391646 | ||||||
| chr16:47392142
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.656-16202C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47392142 | ||||||
| chr16:47392397
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.656-16457A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47392397 | ||||||
| chr16:47392474
|
T | A | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.656-16534A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47392474 | ||||||
| chr16:47392689
|
C | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.656-16749G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47392689 | ||||||
| chr16:47393047
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.656-17107T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47393047 | ||||||
| chr16:47393095
|
G | A | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.656-17155C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47393095 | ||||||
| chr16:47393158
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.656-17218T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47393158 | ||||||
| chr16:47393330
|
C | T | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.656-17390G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47393330 | ||||||
| chr16:47393620
|
A | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.656-17680T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47393620 | ||||||
| chr16:47393745
|
A | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0044 | 2 | HG00140.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.656-17805T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47393745 | ||||||
| chr16:47393832
|
A | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.656-17892T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47393832 | ||||||
| chr16:47394181
|
A | C | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.656-18241T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47394181 | ||||||
| chr16:47394407
|
T | C | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.656-18467A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47394407 | ||||||
| chr16:47395144
|
T | C | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG00735.hp1 HG01169.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.656-19204A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47395144 | ||||||
| chr16:47395281
|
A | T | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-19341T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47395281 | ||||||
| chr16:47395460
|
A | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.656-19520T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47395460 | ||||||
| chr16:47395712
|
C | A | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.656-19772G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47395712 | ||||||
| chr16:47396522
|
T | TTGTGTGT others(3): Show |
7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-20583_656-2058 others(14): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47396522 | ||||||
| chr16:47396522
|
T | TTGTGTGT others(7): Show |
3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.656-20583_656-2058 others(18): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47396522 | ||||||
| chr16:47396522
|
T | TTGTGTGT others(11): Show |
1 | a0001c0002t0002g0085 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.656-20583_656-2058 others(22): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47396522 | ||||||
| chr16:47396522
|
T | TTGTGTGT others(15): Show |
2 | a0001c0002t0001g0067a0001c0002t0002g0090 | 2 | HG01496.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.656-20583_656-2058 others(26): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47396522 | ||||||
| chr16:47396522
|
T | TTGTGTGT others(17): Show |
7 | a0001c0002t0001g0096a0001c0002t0002g0072a0001c0002t0002g0073others(4): Show | 7 | HG01109.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-20583_656-2058 others(28): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47396522 | ||||||
| chr16:47396522
|
T | TTGTGTGT others(19): Show |
8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(5): Show | 8 | HG01074.hp2 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.656-20583_656-2058 others(30): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47396522 | ||||||
| chr16:47396522
|
T | TTGTGTGT others(21): Show |
13 | a0001c0001t0001g0010a0001c0001t0001g0055a0001c0001t0001g0056others(10): Show | 13 | HG01255.hp2 HG01361.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.656-20583_656-2058 others(32): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47396522 | ||||||
| chr16:47396522
|
T | TTGTGTGT others(23): Show |
2 | a0001c0002t0002g0088a0001c0004t0001g0071 | 2 | HG00735.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.656-20583_656-2058 others(34): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47396522 | ||||||
| chr16:47396522
|
T | TTGTGTGT others(25): Show |
1 | a0001c0002t0001g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.656-20583_656-2058 others(36): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47396522 | ||||||
| chr16:47396524
|
T | G | 48 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(45): Show | 48 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.656-20584A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47396524 | ||||||
| chr16:47396629
|
ATATTTGC others(3): Show |
A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.656-20699_656-2069 others(14): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47396629 | ||||||
| chr16:47396633
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005 | 3 | HG01891.hp2 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.656-20693A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47396633 | ||||||
| chr16:47396663
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.656-20723A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47396663 | ||||||
| chr16:47396754
|
C | T | 1 | a0001c0004t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.656-20814G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47396754 | ||||||
| chr16:47396777
|
A | T | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.656-20837T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47396777 | ||||||
| chr16:47396783
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.656-20843G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47396783 | ||||||
| chr16:47397055
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.656-21115G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47397055 | ||||||
| chr16:47397056
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.656-21116C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47397056 | ||||||
| chr16:47397741
|
A | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.656-21801T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47397741 | ||||||
| chr16:47399572
|
C | CA | 6 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(3): Show | 6 | HG01361.hp2 HG01496.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.656-23633dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47399572 | ||||||
| chr16:47399623
|
A | G | 44 | a0001c0001t0001g0002a0001c0001t0001g0063a0001c0001t0001g0066others(41): Show | 44 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.656-23683T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47399623 | ||||||
| chr16:47399651
|
G | A | 3 | a0001c0002t0002g0086a0001c0002t0002g0087a0001c0002t0002g0088 | 3 | HG00735.hp2 HG01074.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.656-23711C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47399651 | ||||||
| chr16:47400086
|
A | T | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.656-24146T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47400086 | ||||||
| chr16:47400263
|
C | A | 27 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(24): Show | 27 | HG00140.hp1 HG00280.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-24323G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47400263 | ||||||
| chr16:47400270
|
T | G | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.656-24330A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47400270 | ||||||
| chr16:47400457
|
T | TAC | 13 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(10): Show | 13 | HG00609.hp2 HG01361.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.656-24519_656-2451 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47400457 | ||||||
| chr16:47400457
|
T | TACAC | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(6): Show | 9 | HG01496.hp1 HG01891.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.656-24521_656-2451 others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47400457 | ||||||
| chr16:47400457
|
T | TACACAC | 2 | a0001c0001t0001g0101a0001c0005t0001g0103 | 2 | HG02109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.656-24523_656-2451 others(10): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47400457 | ||||||
| chr16:47400457
|
TAC | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0109 | 2 | HG00735.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.656-24519_656-2451 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47400457 | ||||||
| chr16:47400457
|
TACAC | T | 2 | a0001c0001t0001g0032a0001c0004t0001g0071 | 2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.656-24521_656-2451 others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47400457 | ||||||
| chr16:47400702
|
GGAGGTAG others(10): Show |
G | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.656-24779_656-2476 others(21): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47400702 | ||||||
| chr16:47400940
|
T | C | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.656-25000A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47400940 | ||||||
| chr16:47401074
|
G | T | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.656-25134C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47401074 | ||||||
| chr16:47401077
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.656-25137C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47401077 | ||||||
| chr16:47401216
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.656-25276T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47401216 | ||||||
| chr16:47401326
|
C | T | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.656-25386G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47401326 | ||||||
| chr16:47401489
|
T | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.656-25549A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47401489 | ||||||
| chr16:47401967
|
G | A | 3 | a0001c0002t0004g0064a0001c0002t0004g0065a0001c0002t0004g0095 | 3 | HG02895.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.656-26027C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47401967 | ||||||
| chr16:47402012
|
G | A | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.656-26072C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47402012 | ||||||
| chr16:47402013
|
T | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.656-26073A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47402013 | ||||||
| chr16:47402032
|
G | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.656-26092C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47402032 | ||||||
| chr16:47402101
|
A | G | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.656-26161T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47402101 | ||||||
| chr16:47402106
|
C | T | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.656-26166G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47402106 | ||||||
| chr16:47402293
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.656-26353T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47402293 | ||||||
| chr16:47402355
|
T | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.656-26415A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47402355 | ||||||
| chr16:47402554
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+26250G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47402554 | ||||||
| chr16:47402908
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.655+25896G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47402908 | ||||||
| chr16:47403602
|
T | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+25202A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47403602 | ||||||
| chr16:47403691
|
G | C | 1 | a0001c0001t0001g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.655+25113C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47403691 | ||||||
| chr16:47403761
|
T | TAC | 34 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0021others(31): Show | 34 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.655+25041_655+2504 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47403761 | ||||||
| chr16:47403761
|
T | TACAC | 11 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0029others(8): Show | 11 | HG00609.hp1 HG01074.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.655+25039_655+2504 others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47403761 | ||||||
| chr16:47403761
|
T | TACACACA others(3): Show |
1 | a0001c0001t0001g0039 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.655+25033_655+2504 others(14): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47403761 | ||||||
| chr16:47403761
|
TAC | T | 18 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0018others(15): Show | 18 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.655+25041_655+2504 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47403761 | ||||||
| chr16:47403761
|
TACAC | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0055others(1): Show | 4 | HG00280.hp1 HG02970.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+25039_655+2504 others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47403761 | ||||||
| chr16:47404064
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0050 | 2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.655+24740T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47404064 | ||||||
| chr16:47404092
|
G | A | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.655+24712C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47404092 | ||||||
| chr16:47404654
|
T | C | 1 | a0001c0001t0001g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.655+24150A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47404654 | ||||||
| chr16:47405053
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0023 | 3 | HG00140.hp2 HG00280.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.655+23751G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47405053 | ||||||
| chr16:47405287
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005 | 3 | HG01891.hp2 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.655+23517G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47405287 | ||||||
| chr16:47405306
|
T | C | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.655+23498A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47405306 | ||||||
| chr16:47405379
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.655+23425C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47405379 | ||||||
| chr16:47405457
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.655+23347T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47405457 | ||||||
| chr16:47405616
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.655+23188A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47405616 | ||||||
| chr16:47405864
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.655+22940C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47405864 | ||||||
| chr16:47406406
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.655+22398G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47406406 | ||||||
| chr16:47407154
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+21650T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47407154 | ||||||
| chr16:47407781
|
T | C | 1 | a0001c0002t0002g0072 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.655+21023A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47407781 | ||||||
| chr16:47407928
|
CCAAGAGT others(3): Show |
C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+20866_655+2087 others(14): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47407928 | ||||||
| chr16:47408037
|
T | G | 25 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(22): Show | 25 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.655+20767A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47408037 | ||||||
| chr16:47408076
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.655+20728A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47408076 | ||||||
| chr16:47408115
|
G | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+20689C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47408115 | ||||||
| chr16:47408517
|
T | C | 1 | a0001c0002t0002g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.655+20287A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47408517 | ||||||
| chr16:47408666
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655+20138T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47408666 | ||||||
| chr16:47409123
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.655+19681C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409123 | ||||||
| chr16:47409374
|
C | CTATATAT others(5): Show |
1 | a0001c0001t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.655+19418_655+1942 others(16): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409374 | ||||||
| chr16:47409374
|
C | CTATATAT others(19): Show |
1 | a0001c0003t0001g0001 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.655+19429_655+1943 others(30): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409374 | ||||||
| chr16:47409374
|
C | CTATATAT others(13): Show |
2 | a0001c0001t0001g0058a0001c0001t0001g0061 | 2 | HG03098.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.655+19410_655+1942 others(24): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409374 | ||||||
| chr16:47409374
|
CTATA | C | 2 | a0001c0001t0001g0029a0001c0001t0003g0098 | 2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.655+19426_655+1942 others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409374 | ||||||
| chr16:47409392
|
ATATATAT others(10): Show |
A | 1 | a0001c0002t0002g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.655+19395_655+1941 others(21): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409392 | ||||||
| chr16:47409394
|
A | T | 1 | a0001c0002t0001g0067 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.655+19410T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409394 | ||||||
| chr16:47409396
|
A | T | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.655+19408T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409396 | ||||||
| chr16:47409398
|
A | T | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.655+19406T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409398 | ||||||
| chr16:47409399
|
TATA | T | 3 | a0001c0001t0001g0028a0001c0001t0003g0068a0001c0001t0003g0097 | 3 | HG01884.hp2 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.655+19402_655+1940 others(7): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409399 | ||||||
| chr16:47409400
|
A | T | 5 | a0001c0001t0001g0045a0001c0001t0003g0069a0001c0001t0003g0092others(2): Show | 5 | HG01496.hp1 HG02109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.655+19404T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409400 | ||||||
| chr16:47409402
|
A | ATT | 4 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0055others(1): Show | 4 | HG02258.hp2 HG02897.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+19401_655+1940 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409402 | ||||||
| chr16:47409402
|
A | ATTT | 2 | a0001c0001t0001g0008a0001c0001t0001g0011 | 2 | HG02896.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.655+19401_655+1940 others(7): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409402 | ||||||
| chr16:47409402
|
A | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0045a0001c0001t0001g0046others(5): Show | 8 | HG01361.hp2 HG01496.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.655+19402T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409402 | ||||||
| chr16:47409403
|
T | TTATATAT others(3): Show |
1 | a0001c0001t0001g0033 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.655+19400_655+1940 others(14): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409403 | ||||||
| chr16:47409404
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.655+19399_655+1940 others(15): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0032a0001c0001t0001g0110 | 2 | HG03453.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.655+19399_655+1940 others(21): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0007 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.655+19399_655+1940 others(44): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0038 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.655+19399_655+1940 others(32): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(23): Show |
1 | a0001c0002t0002g0072 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.655+19399_655+1940 others(34): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.655+19399_655+1940 others(27): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0017a0001c0001t0001g0022 | 2 | HG00280.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.655+19399_655+1940 others(24): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.655+19399_655+1940 others(27): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(21): Show |
1 | a0001c0002t0001g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.655+19399_655+1940 others(32): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0048 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.655+19399_655+1940 others(22): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0020 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.655+19399_655+1940 others(23): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0037 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.655+19399_655+1940 others(28): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(19): Show |
1 | a0001c0002t0002g0081 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.655+19399_655+1940 others(30): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.655+19399_655+1940 others(21): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0015a0001c0001t0001g0047 | 2 | HG01258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.655+19399_655+1940 others(22): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(16): Show |
1 | a0001c0002t0004g0095 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.655+19399_655+1940 others(27): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(19): Show |
1 | a0001c0002t0002g0082 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.655+19399_655+1940 others(30): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0021 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.655+19399_655+1940 others(18): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0030 | 3 | HG00741.hp1 HG01496.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.655+19399_655+1940 others(19): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(10): Show |
1 | a0001c0002t0002g0093 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.655+19399_655+1940 others(21): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0049 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.655+19399_655+1940 others(22): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(16): Show |
1 | a0001c0002t0002g0078 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.655+19399_655+1940 others(27): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(24): Show |
1 | a0001c0002t0002g0084 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.655+19399_655+1940 others(35): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.655+19399_655+1940 others(16): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0043a0001c0001t0001g0054 | 2 | HG00609.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.655+19399_655+1940 others(17): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0023a0001c0001t0001g0039 | 2 | HG00280.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.655+19399_655+1940 others(18): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(10): Show |
1 | a0001c0002t0002g0086 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.655+19399_655+1940 others(21): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(12): Show |
2 | a0001c0002t0004g0064a0001c0002t0004g0065 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.655+19399_655+1940 others(23): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(3): Show |
2 | a0001c0001t0001g0018a0001c0001t0001g0060 | 2 | NA21309.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.655+19399_655+1940 others(14): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0053 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.655+19399_655+1940 others(15): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.655+19399_655+1940 others(18): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.655+19399_655+1940 others(20): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(15): Show |
1 | a0001c0002t0002g0076 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.655+19399_655+1940 others(26): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(4): Show |
1 | a0001c0002t0002g0087 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.655+19399_655+1940 others(15): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(6): Show |
3 | a0001c0001t0001g0006a0001c0001t0001g0100a0001c0002t0002g0088 | 3 | HG00735.hp2 HG01169.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.655+19399_655+1940 others(17): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655+19399_655+1940 others(20): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(10): Show |
1 | a0001c0002t0002g0085 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.655+19399_655+1940 others(21): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATATAT others(17): Show |
1 | a0001c0002t0002g0083 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.655+19399_655+1940 others(28): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATTTTT | 4 | a0001c0001t0001g0099a0001c0001t0001g0107a0001c0001t0001g0108others(1): Show | 4 | HG00735.hp1 HG01169.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+19399_655+1940 others(11): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATTTTT others(4): Show |
1 | a0001c0002t0002g0077 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.655+19399_655+1940 others(15): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATATTTTT others(8): Show |
1 | a0001c0002t0002g0074 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.655+19399_655+1940 others(19): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | ATTTTTTT others(4): Show |
1 | a0001c0002t0002g0073 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.655+19389_655+1939 others(15): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
A | T | 24 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(21): Show | 24 | HG00642.hp1 HG00741.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.655+19400T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409404
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0004t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.655+19389_655+1939 others(15): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409404 | ||||||
| chr16:47409405
|
T | TATATATA others(6): Show |
1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.655+19398_655+1939 others(17): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409405 | ||||||
| chr16:47409405
|
T | TATATATA others(8): Show |
1 | a0001c0001t0001g0031 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.655+19398_655+1939 others(19): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409405 | ||||||
| chr16:47409406
|
T | A | 6 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0104others(3): Show | 6 | HG00642.hp2 HG02109.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+19398A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409406 | ||||||
| chr16:47409407
|
T | A | 2 | a0001c0001t0001g0031a0001c0002t0002g0075 | 2 | HG01891.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.655+19397A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409407 | ||||||
| chr16:47409408
|
T | A | 4 | a0001c0001t0001g0058a0001c0001t0001g0104a0001c0001t0001g0106others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.655+19396A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409408 | ||||||
| chr16:47409409
|
T | A | 2 | a0001c0001t0001g0031a0001c0002t0002g0075 | 2 | HG01891.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.655+19395A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409409 | ||||||
| chr16:47409410
|
T | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0005t0001g0103 | 3 | HG02109.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+19394A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409410 | ||||||
| chr16:47409411
|
T | A | 1 | a0001c0002t0001g0079 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.655+19393A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409411 | ||||||
| chr16:47409412
|
T | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0002t0001g0080 | 3 | HG02970.hp1 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+19392A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409412 | ||||||
| chr16:47409414
|
T | A | 1 | a0001c0001t0001g0106 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.655+19390A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409414 | ||||||
| chr16:47409417
|
T | A | 1 | a0001c0004t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.655+19387A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409417 | ||||||
| chr16:47409719
|
A | C | 3 | a0001c0002t0002g0082a0001c0002t0002g0083a0001c0002t0002g0084 | 3 | HG02257.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.655+19085T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409719 | ||||||
| chr16:47409788
|
A | AAC | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+19014_655+1901 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47409788 | ||||||
| chr16:47410202
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+18602G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47410202 | ||||||
| chr16:47410244
|
A | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.655+18560T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47410244 | ||||||
| chr16:47410296
|
T | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.655+18508A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47410296 | ||||||
| chr16:47410695
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.655+18109G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47410695 | ||||||
| chr16:47410831
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.655+17973G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47410831 | ||||||
| chr16:47410935
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.655+17869A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47410935 | ||||||
| chr16:47411797
|
T | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+17007A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47411797 | ||||||
| chr16:47411825
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.655+16979G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47411825 | ||||||
| chr16:47411858
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.655+16946G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47411858 | ||||||
| chr16:47411888
|
A | G | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.655+16916T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47411888 | ||||||
| chr16:47412063
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+16741G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47412063 | ||||||
| chr16:47412386
|
A | G | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.655+16418T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47412386 | ||||||
| chr16:47412652
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.655+16152G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47412652 | ||||||
| chr16:47412669
|
C | T | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.655+16135G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47412669 | ||||||
| chr16:47412695
|
CA | C | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 62 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.655+16108delT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47412695 | ||||||
| chr16:47412695
|
CAA | C | 35 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0032others(32): Show | 35 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.655+16107_655+1610 others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47412695 | ||||||
| chr16:47413330
|
A | C | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.655+15474T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47413330 | ||||||
| chr16:47413493
|
A | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.655+15311T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47413493 | ||||||
| chr16:47414229
|
A | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.655+14575T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47414229 | ||||||
| chr16:47414398
|
T | C | 1 | a0001c0002t0002g0077 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.655+14406A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47414398 | ||||||
| chr16:47414552
|
AAAC | A | 36 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(33): Show | 36 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.655+14249_655+1425 others(7): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47414552 | ||||||
| chr16:47415131
|
C | T | 2 | a0001c0002t0002g0082a0001c0002t0002g0083 | 2 | HG02257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.655+13673G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47415131 | ||||||
| chr16:47415132
|
G | A | 4 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0091others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.655+13672C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47415132 | ||||||
| chr16:47415524
|
A | C | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.655+13280T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47415524 | ||||||
| chr16:47415923
|
G | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.655+12881C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47415923 | ||||||
| chr16:47416016
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.655+12788G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47416016 | ||||||
| chr16:47416082
|
G | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.655+12722C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47416082 | ||||||
| chr16:47416182
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0058 | 2 | HG02735.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.655+12622G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47416182 | ||||||
| chr16:47416469
|
G | C | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.655+12335C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47416469 | ||||||
| chr16:47416863
|
G | T | 4 | a0001c0002t0001g0094a0001c0002t0002g0082a0001c0002t0002g0083others(1): Show | 4 | HG02257.hp2 HG02922.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+11941C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47416863 | ||||||
| chr16:47416883
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.655+11921C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47416883 | ||||||
| chr16:47416988
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.655+11816A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47416988 | ||||||
| chr16:47417726
|
G | A | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.655+11078C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47417726 | ||||||
| chr16:47417824
|
T | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+10980A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47417824 | ||||||
| chr16:47417867
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.655+10937C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47417867 | ||||||
| chr16:47418375
|
G | C | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.655+10429C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47418375 | ||||||
| chr16:47418934
|
C | A | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.655+9870G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47418934 | ||||||
| chr16:47419169
|
G | A | 9 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0033others(6): Show | 9 | HG00140.hp1 HG00642.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.655+9635C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47419169 | ||||||
| chr16:47419276
|
A | AT | 36 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(33): Show | 36 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.655+9527dupA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47419276 | ||||||
| chr16:47419379
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.655+9425G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47419379 | ||||||
| chr16:47419460
|
C | T | 3 | a0001c0002t0002g0086a0001c0002t0002g0087a0001c0002t0002g0088 | 3 | HG00735.hp2 HG01074.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.655+9344G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47419460 | ||||||
| chr16:47419598
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.655+9206C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47419598 | ||||||
| chr16:47419601
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.655+9203G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47419601 | ||||||
| chr16:47419601
|
CT | C | 53 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(50): Show | 53 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.655+9202delA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47419601 | ||||||
| chr16:47419624
|
T | TGA | 5 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.655+9178_655+9179d others(4): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47419624 | ||||||
| chr16:47419701
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.655+9103G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47419701 | ||||||
| chr16:47419944
|
TTTATC | T | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.655+8855_655+8859d others(7): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47419944 | ||||||
| chr16:47420053
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+8751T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47420053 | ||||||
| chr16:47420512
|
T | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.655+8292A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47420512 | ||||||
| chr16:47420821
|
C | CT | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+7982dupA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47420821 | ||||||
| chr16:47420929
|
C | T | 1 | a0001c0001t0001g0018 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.655+7875G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47420929 | ||||||
| chr16:47421050
|
A | T | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.655+7754T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47421050 | ||||||
| chr16:47421270
|
G | GCA | 30 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(27): Show | 30 | HG00735.hp2 HG01074.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.655+7532_655+7533d others(4): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47421270 | ||||||
| chr16:47421270
|
G | GCACA | 5 | a0001c0001t0001g0032a0001c0001t0003g0097a0001c0001t0003g0098others(2): Show | 5 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.655+7530_655+7533d others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47421270 | ||||||
| chr16:47421270
|
G | GCACACA | 2 | a0001c0002t0002g0076a0001c0002t0004g0095 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.655+7528_655+7533d others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47421270 | ||||||
| chr16:47421270
|
GCA | G | 9 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0019others(6): Show | 9 | HG00741.hp1 HG02735.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.655+7532_655+7533d others(4): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47421270 | ||||||
| chr16:47421270
|
GCACACA | G | 4 | a0001c0001t0001g0035a0001c0001t0001g0104a0001c0001t0001g0105others(1): Show | 4 | HG02280.hp1 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+7528_655+7533d others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47421270 | ||||||
| chr16:47421291
|
CACACACA others(9): Show |
C | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.655+7497_655+7512d others(18): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47421291 | ||||||
| chr16:47421301
|
CACACAT | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0002t0001g0096 | 3 | HG02723.hp1 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.655+7497_655+7502d others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47421301 | ||||||
| chr16:47421305
|
CAT | C | 4 | a0001c0001t0001g0034a0001c0001t0003g0068a0001c0002t0002g0078others(1): Show | 4 | HG01109.hp2 HG02602.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+7497_655+7498d others(4): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47421305 | ||||||
| chr16:47421307
|
T | C | 27 | a0001c0001t0003g0069a0001c0001t0003g0070a0001c0001t0003g0091others(24): Show | 27 | HG00735.hp2 HG01074.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.655+7497A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47421307 | ||||||
| chr16:47421410
|
T | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005 | 3 | HG01891.hp2 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.655+7394A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47421410 | ||||||
| chr16:47421460
|
A | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+7344T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47421460 | ||||||
| chr16:47421707
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0023 | 3 | HG00140.hp2 HG00280.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.655+7097G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47421707 | ||||||
| chr16:47421843
|
A | G | 41 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.655+6961T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47421843 | ||||||
| chr16:47422158
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.655+6646A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47422158 | ||||||
| chr16:47422320
|
C | T | 1 | a0001c0004t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.655+6484G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47422320 | ||||||
| chr16:47422472
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.655+6332G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47422472 | ||||||
| chr16:47422699
|
C | G | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.655+6105G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47422699 | ||||||
| chr16:47423121
|
T | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0038others(3): Show | 6 | HG02055.hp2 HG02559.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+5683A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47423121 | ||||||
| chr16:47423251
|
AT | A | 29 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(26): Show | 29 | HG00140.hp1 HG00280.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.655+5552delA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47423251 | ||||||
| chr16:47423299
|
C | G | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.655+5505G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47423299 | ||||||
| chr16:47423314
|
G | C | 23 | a0001c0002t0001g0094a0001c0002t0002g0072a0001c0002t0002g0073others(20): Show | 23 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.655+5490C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47423314 | ||||||
| chr16:47423479
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.655+5325A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47423479 | ||||||
| chr16:47423484
|
G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0054 | 3 | HG00280.hp2 HG00609.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.655+5320C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47423484 | ||||||
| chr16:47423493
|
T | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.655+5311A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47423493 | ||||||
| chr16:47423858
|
A | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0058 | 2 | HG02735.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.655+4946T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47423858 | ||||||
| chr16:47423953
|
T | C | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.655+4851A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47423953 | ||||||
| chr16:47424206
|
C | A | 1 | a0001c0001t0001g0054 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.655+4598G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47424206 | ||||||
| chr16:47424708
|
TG | T | 12 | a0001c0002t0002g0072a0001c0002t0002g0073a0001c0002t0002g0074others(9): Show | 12 | HG01109.hp2 HG01891.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.655+4095delC | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47424708 | ||||||
| chr16:47424885
|
T | G | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.655+3919A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47424885 | ||||||
| chr16:47424886
|
T | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.655+3918A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47424886 | ||||||
| chr16:47424921
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.655+3883G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47424921 | ||||||
| chr16:47424939
|
G | A | 28 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(25): Show | 28 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.655+3865C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47424939 | ||||||
| chr16:47425210
|
T | C | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.655+3594A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47425210 | ||||||
| chr16:47425245
|
T | C | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.655+3559A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47425245 | ||||||
| chr16:47425436
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.655+3368G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47425436 | ||||||
| chr16:47425474
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.655+3330C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47425474 | ||||||
| chr16:47425589
|
C | CT | 6 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(3): Show | 6 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+3214dupA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47425589 | ||||||
| chr16:47425589
|
CT | C | 41 | a0001c0001t0001g0063a0001c0001t0001g0100a0001c0001t0001g0101others(38): Show | 41 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.655+3214delA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47425589 | ||||||
| chr16:47425651
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.655+3153C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47425651 | ||||||
| chr16:47425717
|
T | C | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.655+3087A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47425717 | ||||||
| chr16:47425731
|
C | A | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.655+3073G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47425731 | ||||||
| chr16:47425742
|
G | A | 1 | a0001c0002t0002g0093 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.655+3062C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47425742 | ||||||
| chr16:47426003
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0063 | 2 | HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.655+2801G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47426003 | ||||||
| chr16:47426039
|
A | G | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.655+2765T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47426039 | ||||||
| chr16:47426235
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.655+2569C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47426235 | ||||||
| chr16:47426961
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.655+1843A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47426961 | ||||||
| chr16:47427010
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.655+1794G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47427010 | ||||||
| chr16:47427141
|
C | A | 1 | a0001c0001t0001g0059 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.655+1663G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47427141 | ||||||
| chr16:47427284
|
T | C | 45 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(42): Show | 45 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.655+1520A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47427284 | ||||||
| chr16:47427438
|
C | A | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.655+1366G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47427438 | ||||||
| chr16:47427445
|
TCTGGAGT others(11): Show |
T | 1 | a0001c0001t0001g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.655+1341_655+1358d others(20): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47427445 | ||||||
| chr16:47427511
|
A | T | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.655+1293T>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47427511 | ||||||
| chr16:47427612
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.655+1192G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47427612 | ||||||
| chr16:47427656
|
A | AGTAACAT | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.655+1141_655+1147d others(9): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47427656 | ||||||
| chr16:47427671
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG01258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.655+1133G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47427671 | ||||||
| chr16:47428480
|
T | C | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.655+324A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47428480 | ||||||
| chr16:47428536
|
CAT | C | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG00735.hp1 HG01169.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.655+266_655+267del others(2): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47428536 | ||||||
| chr16:47428747
|
T | G | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.655+57A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 6/17 | chr16 | 47428747 | ||||||
| chr16:47428940
|
A | G | 26 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(23): Show | 26 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.561-42T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47428940 | ||||||
| chr16:47428960
|
T | TAAAAATC others(312): Show |
1 | a0001c0001t0003g0070 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.561-63_561-62insTT others(317): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47428960 | ||||||
| chr16:47429635
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.561-737C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47429635 | ||||||
| chr16:47430088
|
C | T | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.561-1190G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47430088 | ||||||
| chr16:47430103
|
G | T | 1 | a0001c0001t0001g0109 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.561-1205C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47430103 | ||||||
| chr16:47430136
|
C | T | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG00140.hp1 HG00280.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.561-1238G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47430136 | ||||||
| chr16:47431037
|
G | T | 24 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(21): Show | 24 | HG00140.hp1 HG00280.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.561-2139C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47431037 | ||||||
| chr16:47431088
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0023 | 2 | HG00140.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.561-2190C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47431088 | ||||||
| chr16:47431358
|
C | T | 1 | a0001c0003t0001g0001 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.561-2460G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47431358 | ||||||
| chr16:47432236
|
G | A | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.561-3338C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47432236 | ||||||
| chr16:47432263
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.561-3365A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47432263 | ||||||
| chr16:47432896
|
G | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | HG00642.hp1 HG00741.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.561-3998C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47432896 | ||||||
| chr16:47433491
|
A | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.561-4593T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433491 | ||||||
| chr16:47433603
|
CTA | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0026 | 2 | HG00140.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.561-4707_561-4706d others(4): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433603 | ||||||
| chr16:47433770
|
A | AAT | 7 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0015others(4): Show | 7 | HG00280.hp2 HG00609.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-4874_561-4873d others(4): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433770 | ||||||
| chr16:47433770
|
A | AATATAT | 5 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-4878_561-4873d others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433770 | ||||||
| chr16:47433770
|
A | AATATATA others(1): Show |
7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0002t0001g0094others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-4880_561-4873d others(10): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433770 | ||||||
| chr16:47433770
|
A | AATATATA others(3): Show |
15 | a0001c0001t0001g0102a0001c0002t0002g0072a0001c0002t0002g0073others(12): Show | 15 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.561-4882_561-4873d others(12): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433770 | ||||||
| chr16:47433770
|
A | AATATATA others(5): Show |
4 | a0001c0002t0002g0075a0001c0002t0002g0076a0001c0004t0001g0071others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-4884_561-4873d others(14): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433770 | ||||||
| chr16:47433791
|
A | ATATATAT others(1): Show |
2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.561-4894_561-4893i others(10): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433791 | ||||||
| chr16:47433792
|
T | TATATATA others(1): Show |
3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0002t0002g0090 | 3 | HG02717.hp2 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.561-4895_561-4894i others(10): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433792 | ||||||
| chr16:47433792
|
T | TATATATA others(3): Show |
2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.561-4895_561-4894i others(12): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433792 | ||||||
| chr16:47433792
|
T | TATATATA others(5): Show |
2 | a0001c0002t0001g0079a0001c0002t0001g0080 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.561-4895_561-4894i others(14): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433792 | ||||||
| chr16:47433857
|
A | AATATAT | 2 | a0001c0001t0001g0037a0001c0001t0001g0053 | 2 | HG02056.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.561-4965_561-4960d others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433857 | ||||||
| chr16:47433857
|
AAT | A | 12 | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0032others(9): Show | 12 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.561-4961_561-4960d others(4): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433857 | ||||||
| chr16:47433857
|
AATAT | A | 12 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0016others(9): Show | 12 | HG00735.hp1 HG01109.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.561-4963_561-4960d others(6): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433857 | ||||||
| chr16:47433857
|
AATATAT | A | 13 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(10): Show | 13 | HG00280.hp1 HG00609.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.561-4965_561-4960d others(8): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433857 | ||||||
| chr16:47433857
|
AATATATA others(1): Show |
A | 7 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0031others(4): Show | 7 | HG00140.hp1 HG00609.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-4967_561-4960d others(10): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433857 | ||||||
| chr16:47433857
|
AATATATA others(3): Show |
A | 9 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(6): Show | 9 | HG00140.hp2 HG01891.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.561-4969_561-4960d others(12): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433857 | ||||||
| chr16:47433857
|
AATATATA others(5): Show |
A | 8 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(5): Show | 8 | HG01361.hp2 HG02280.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.561-4971_561-4960d others(14): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433857 | ||||||
| chr16:47433857
|
AATATATA others(7): Show |
A | 3 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0002t0001g0096 | 3 | HG02723.hp1 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.561-4973_561-4960d others(16): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433857 | ||||||
| chr16:47433857
|
AATATATA others(9): Show |
A | 8 | a0001c0001t0001g0101a0001c0001t0003g0069a0001c0001t0003g0070others(5): Show | 8 | HG01255.hp2 HG01361.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.561-4975_561-4960d others(18): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433857 | ||||||
| chr16:47433857
|
AATATATA others(11): Show |
A | 11 | a0001c0001t0001g0049a0001c0001t0001g0104a0001c0001t0001g0105others(8): Show | 11 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.561-4977_561-4960d others(20): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433857 | ||||||
| chr16:47433857
|
AATATATA others(13): Show |
A | 7 | a0001c0001t0001g0066a0001c0001t0003g0068a0001c0001t0003g0098others(4): Show | 7 | HG01074.hp2 HG01109.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-4979_561-4960d others(22): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433857 | ||||||
| chr16:47433857
|
AATATATA others(15): Show |
A | 6 | a0001c0002t0002g0072a0001c0002t0002g0081a0001c0002t0002g0089others(3): Show | 6 | HG02630.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.561-4981_561-4960d others(24): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433857 | ||||||
| chr16:47433857
|
AATATATA others(17): Show |
A | 6 | a0001c0002t0001g0067a0001c0002t0002g0075a0001c0002t0002g0076others(3): Show | 6 | HG01496.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.561-4983_561-4960d others(26): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433857 | ||||||
| chr16:47433857
|
AATATATA others(21): Show |
A | 2 | a0001c0001t0001g0002a0001c0001t0001g0063 | 2 | HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.561-4987_561-4960d others(30): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433857 | ||||||
| chr16:47433910
|
G | A | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.561-5012C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47433910 | ||||||
| chr16:47434179
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.561-5281G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47434179 | ||||||
| chr16:47434430
|
C | A | 1 | a0001c0001t0001g0022 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.561-5532G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47434430 | ||||||
| chr16:47434615
|
T | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.561-5717A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47434615 | ||||||
| chr16:47434751
|
C | T | 1 | a0001c0004t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.561-5853G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47434751 | ||||||
| chr16:47434752
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.561-5854C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47434752 | ||||||
| chr16:47434953
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.561-6055G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47434953 | ||||||
| chr16:47435445
|
C | T | 4 | a0001c0002t0002g0075a0001c0002t0002g0076a0001c0002t0002g0085others(1): Show | 4 | HG01891.hp1 HG02258.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-6547G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47435445 | ||||||
| chr16:47435574
|
T | C | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.561-6676A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47435574 | ||||||
| chr16:47436251
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.561-7353C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47436251 | ||||||
| chr16:47436361
|
G | A | 2 | a0001c0002t0002g0087a0001c0002t0002g0088 | 2 | HG00735.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.561-7463C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47436361 | ||||||
| chr16:47436365
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.561-7467T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47436365 | ||||||
| chr16:47436836
|
C | A | 1 | a0001c0001t0001g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.561-7938G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47436836 | ||||||
| chr16:47437422
|
C | T | 10 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0033others(7): Show | 10 | HG00140.hp1 HG00642.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.561-8524G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47437422 | ||||||
| chr16:47437705
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.561-8807C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47437705 | ||||||
| chr16:47437958
|
C | T | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.561-9060G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47437958 | ||||||
| chr16:47438003
|
C | T | 37 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(34): Show | 37 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.561-9105G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47438003 | ||||||
| chr16:47438110
|
G | A | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.561-9212C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47438110 | ||||||
| chr16:47438130
|
G | A | 2 | a0001c0002t0002g0073a0001c0002t0002g0074 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.561-9232C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47438130 | ||||||
| chr16:47438686
|
C | T | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.561-9788G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47438686 | ||||||
| chr16:47438909
|
C | A | 1 | a0001c0001t0001g0051 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.561-10011G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47438909 | ||||||
| chr16:47439033
|
C | T | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.561-10135G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47439033 | ||||||
| chr16:47439153
|
C | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-10255G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47439153 | ||||||
| chr16:47439247
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.561-10349A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47439247 | ||||||
| chr16:47439809
|
T | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.561-10911A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47439809 | ||||||
| chr16:47439944
|
T | C | 1 | a0001c0002t0001g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.561-11046A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47439944 | ||||||
| chr16:47439947
|
C | T | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.561-11049G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47439947 | ||||||
| chr16:47440043
|
CTGATAAA others(8): Show |
C | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.561-11160_561-1114 others(19): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47440043 | ||||||
| chr16:47440451
|
T | G | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.560+10945A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47440451 | ||||||
| chr16:47440456
|
T | A | 1 | a0001c0001t0001g0054 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.560+10940A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47440456 | ||||||
| chr16:47440543
|
C | T | 1 | a0001c0002t0001g0067 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.560+10853G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47440543 | ||||||
| chr16:47440545
|
C | G | 1 | a0001c0002t0001g0067 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.560+10851G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47440545 | ||||||
| chr16:47440629
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.560+10767G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47440629 | ||||||
| chr16:47440644
|
CA | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG01496.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.560+10751delT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47440644 | ||||||
| chr16:47440698
|
G | C | 4 | a0001c0002t0001g0094a0001c0002t0002g0082a0001c0002t0002g0083others(1): Show | 4 | HG02257.hp2 HG02922.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+10698C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47440698 | ||||||
| chr16:47440854
|
G | A | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.560+10542C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47440854 | ||||||
| chr16:47440980
|
C | T | 2 | a0001c0002t0002g0073a0001c0002t0002g0074 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.560+10416G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47440980 | ||||||
| chr16:47441057
|
G | C | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.560+10339C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47441057 | ||||||
| chr16:47441357
|
C | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.560+10039G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47441357 | ||||||
| chr16:47441420
|
C | A | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.560+9976G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47441420 | ||||||
| chr16:47441488
|
C | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0058 | 2 | HG02735.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.560+9908G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47441488 | ||||||
| chr16:47441617
|
T | C | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.560+9779A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47441617 | ||||||
| chr16:47441860
|
A | C | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | HG02280.hp1 HG02970.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+9536T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47441860 | ||||||
| chr16:47442365
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.560+9031T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47442365 | ||||||
| chr16:47442450
|
C | G | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.560+8946G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47442450 | ||||||
| chr16:47442694
|
C | T | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.560+8702G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47442694 | ||||||
| chr16:47443361
|
CTAGAAAT others(115): Show |
C | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.560+7913_560+8034d others(2): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47443361 | ||||||
| chr16:47443468
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0058 | 2 | HG02735.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.560+7928T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47443468 | ||||||
| chr16:47443485
|
G | T | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.560+7911C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47443485 | ||||||
| chr16:47443736
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.560+7660G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47443736 | ||||||
| chr16:47443737
|
G | C | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.560+7659C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47443737 | ||||||
| chr16:47443742
|
C | A | 1 | a0001c0001t0001g0053 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.560+7654G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47443742 | ||||||
| chr16:47443822
|
C | T | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.560+7574G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47443822 | ||||||
| chr16:47443837
|
T | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.560+7559A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47443837 | ||||||
| chr16:47444296
|
C | T | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.560+7100G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47444296 | ||||||
| chr16:47444562
|
T | C | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.560+6834A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47444562 | ||||||
| chr16:47444802
|
T | G | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.560+6594A>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47444802 | ||||||
| chr16:47444952
|
T | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.560+6444A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47444952 | ||||||
| chr16:47445020
|
C | T | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.560+6376G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47445020 | ||||||
| chr16:47445052
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.560+6344G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47445052 | ||||||
| chr16:47445111
|
TA | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0108others(2): Show | 5 | HG01255.hp1 HG01496.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.560+6284delT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47445111 | ||||||
| chr16:47445111
|
TAA | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.560+6283_560+6284d others(4): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47445111 | ||||||
| chr16:47445120
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG02622.hp2 HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.560+6276T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47445120 | ||||||
| chr16:47445247
|
G | GA | 10 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0057others(7): Show | 10 | HG00609.hp2 HG00735.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.560+6148dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47445247 | ||||||
| chr16:47445247
|
GA | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0027others(3): Show | 6 | HG01074.hp1 HG01169.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.560+6148delT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47445247 | ||||||
| chr16:47445627
|
C | A | 39 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(36): Show | 39 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.560+5769G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47445627 | ||||||
| chr16:47445645
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.560+5751T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47445645 | ||||||
| chr16:47446215
|
G | A | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.560+5181C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47446215 | ||||||
| chr16:47446463
|
C | T | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.560+4933G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47446463 | ||||||
| chr16:47447253
|
A | G | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.560+4143T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47447253 | ||||||
| chr16:47447826
|
G | T | 1 | a0001c0002t0002g0072 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.560+3570C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47447826 | ||||||
| chr16:47447962
|
T | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.560+3434A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47447962 | ||||||
| chr16:47448320
|
T | C | 1 | a0001c0004t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.560+3076A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47448320 | ||||||
| chr16:47448492
|
G | T | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.560+2904C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47448492 | ||||||
| chr16:47448549
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.560+2847A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47448549 | ||||||
| chr16:47448604
|
A | AT | 24 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(21): Show | 24 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.560+2791dupA | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47448604 | ||||||
| chr16:47448604
|
A | ATT | 12 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(9): Show | 12 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.560+2790_560+2791d others(4): Show |
ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47448604 | ||||||
| chr16:47449123
|
G | A | 2 | a0001c0002t0001g0067a0001c0002t0001g0096 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.560+2273C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47449123 | ||||||
| chr16:47449729
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.560+1667C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47449729 | ||||||
| chr16:47449774
|
T | C | 3 | a0001c0002t0002g0086a0001c0002t0002g0087a0001c0002t0002g0088 | 3 | HG00735.hp2 HG01074.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.560+1622A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47449774 | ||||||
| chr16:47450033
|
A | G | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.560+1363T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47450033 | ||||||
| chr16:47450111
|
G | T | 1 | a0001c0001t0001g0024 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.560+1285C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47450111 | ||||||
| chr16:47450454
|
C | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.560+942G>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47450454 | ||||||
| chr16:47450685
|
A | C | 1 | a0001c0004t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.560+711T>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47450685 | ||||||
| chr16:47450928
|
C | T | 42 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(39): Show | 42 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.560+468G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47450928 | ||||||
| chr16:47451101
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.560+295G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 5/17 | chr16 | 47451101 | ||||||
| chr16:47451788
|
G | C | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.486-318C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 4/17 | chr16 | 47451788 | ||||||
| chr16:47451859
|
C | G | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.486-389G>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 4/17 | chr16 | 47451859 | ||||||
| chr16:47452648
|
T | C | 25 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0094others(22): Show | 25 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.485+85A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 4/17 | chr16 | 47452648 | ||||||
| chr16:47452906
|
C | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.428-116G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 3/17 | chr16 | 47452906 | ||||||
| chr16:47453084
|
G | C | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.428-294C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 3/17 | chr16 | 47453084 | ||||||
| chr16:47453229
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.428-439G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 3/17 | chr16 | 47453229 | ||||||
| chr16:47453395
|
G | C | 33 | a0001c0001t0001g0066a0001c0001t0003g0068a0001c0001t0003g0069others(30): Show | 33 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.428-605C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 3/17 | chr16 | 47453395 | ||||||
| chr16:47453488
|
A | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.427+525T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 3/17 | chr16 | 47453488 | ||||||
| chr16:47454185
|
T | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.282-27A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 2/17 | chr16 | 47454185 | ||||||
| chr16:47454349
|
G | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG01169.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.282-191C>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 2/17 | chr16 | 47454349 | ||||||
| chr16:47454393
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.282-235G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 2/17 | chr16 | 47454393 | ||||||
| chr16:47454878
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.282-720G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 2/17 | chr16 | 47454878 | ||||||
| chr16:47455339
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.282-1181C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 2/17 | chr16 | 47455339 | ||||||
| chr16:47455430
|
C | T | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.282-1272G>A | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 2/17 | chr16 | 47455430 | ||||||
| chr16:47455777
|
C | CA | 15 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(12): Show | 15 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.282-1620dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 2/17 | chr16 | 47455777 | ||||||
| chr16:47455777
|
CA | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(3): Show | 6 | HG01891.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.282-1620delT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 2/17 | chr16 | 47455777 | ||||||
| chr16:47456539
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.282-2381T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 2/17 | chr16 | 47456539 | ||||||
| chr16:47456562
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.282-2404A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 2/17 | chr16 | 47456562 | ||||||
| chr16:47456692
|
T | TA | 4 | a0001c0001t0001g0102a0001c0002t0001g0096a0001c0002t0004g0095others(1): Show | 4 | HG02109.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.281+2410dupT | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 2/17 | chr16 | 47456692 | ||||||
| chr16:47457202
|
T | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.281+1901A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 2/17 | chr16 | 47457202 | ||||||
| chr16:47457605
|
T | C | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.281+1498A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 2/17 | chr16 | 47457605 | ||||||
| chr16:47457850
|
T | C | 38 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0101others(35): Show | 38 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.281+1253A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 2/17 | chr16 | 47457850 | ||||||
| chr16:47458001
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.281+1102A>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 2/17 | chr16 | 47458001 | ||||||
| chr16:47458541
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.281+562T>C | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 2/17 | chr16 | 47458541 | ||||||
| chr16:47459072
|
G | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.281+31C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 2/17 | chr16 | 47459072 | ||||||
| chr16:47459456
|
T | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02970.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.209-281A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 1/17 | chr16 | 47459456 | ||||||
| chr16:47460023
|
G | C | 1 | a0001c0005t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.208+815C>G | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 1/17 | chr16 | 47460023 | ||||||
| chr16:47460069
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02280.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.208+769C>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 1/17 | chr16 | 47460069 | ||||||
| chr16:47460589
|
T | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG00735.hp1 HG01169.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.208+249A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 1/17 | chr16 | 47460589 | ||||||
| chr16:47460776
|
T | A | 1 | a0001c0001t0001g0110 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.208+62A>T | ITFG1 | ENSG00000129636.13 | transcript | ENST00000320640.11 | protein_coding | 1/17 | chr16 | 47460776 |