Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 80173 |
|---|---|
| ensemblid | ENSG00000096872.17 |
| hgncid | 21424 |
| symbol | IFT74 |
| name | intraflagellar transport 74 |
| refseq_nuc | NM_025103.4 |
| refseq_prot | NP_079379.2 |
| ensembl_nuc | ENST00000380062.10 |
| ensembl_prot | ENSP00000369402.5 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 26956412 |
| end | 27066134 |
| strand | + |
| ver | v1.2 |
| region | chr9:26956412-27066134 |
| region5000 | chr9:26951412-27071134 |
| regionname0 | IFT74_chr9_26956412_27066134 |
| regionname5000 | IFT74_chr9_26951412_27071134 |
| 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 | 600 | 200 | 66 | 37 | 60 | 9 | 26 | 43 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0002 | 0/0 | 600 | 64 | 1 | 15 | 45 | 0 | 3 | 35 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0003 | 0/0 | 600 | 25 | 8 | 3 | 11 | 0 | 3 | 9 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0004 | 0/0 | 600 | 14 | 2 | 2 | 3 | 0 | 7 | 3 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0005 | 0/0 | 600 | 14 | 0 | 4 | 5 | 1 | 4 | 4 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0006 | 0/0 | 600 | 13 | 5 | 3 | 0 | 2 | 3 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0007 | 0/0 | 600 | 7 | 5 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0008 | 0/0 | 600 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0009 | 0/0 | 600 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0010 | 0/0 | 600 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0011 | 0/0 | 600 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0012 | 0/0 | 600 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| 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 | 1803 | 196 | 66 | 33 | 60 | 9 | 26 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| c0002 | 0/0 | 1803 | 64 | 1 | 15 | 45 | 0 | 3 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| c0003 | 0/0 | 1803 | 25 | 8 | 3 | 11 | 0 | 3 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| c0004 | 0/0 | 1803 | 14 | 0 | 4 | 5 | 1 | 4 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| c0005 | 0/0 | 1803 | 14 | 2 | 2 | 3 | 0 | 7 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| c0006 | 0/0 | 1803 | 13 | 5 | 3 | 0 | 2 | 3 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| c0007 | 0/0 | 1803 | 7 | 5 | 2 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| c0008 | 0/0 | 1803 | 3 | 0 | 3 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| c0009 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| c0010 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| c0011 | 0/0 | 1803 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| c0012 | 0/0 | 1803 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| c0013 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| c0014 | 0/0 | 1803 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| 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 | 3523 | 158 | 45 | 23 | 54 | 8 | 26 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0002 | 0/0 | 3523 | 87 | 9 | 18 | 55 | 0 | 5 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0003 | 0/0 | 3523 | 24 | 2 | 16 | 0 | 3 | 3 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0004 | 0/0 | 3511 | 13 | 0 | 3 | 5 | 1 | 4 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0005 | 0/0 | 3511 | 12 | 0 | 2 | 3 | 0 | 7 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0006 | 0/0 | 3523 | 5 | 4 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0007 | 0/0 | 3523 | 5 | 4 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0008 | 0/0 | 3523 | 3 | 3 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0009 | 0/0 | 3523 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0010 | 0/0 | 3523 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0011 | 0/0 | 3523 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0012 | 0/0 | 3511 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0013 | 0/0 | 3523 | 2 | 0 | 0 | 2 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0014 | 0/0 | 3523 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0015 | 0/0 | 3523 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0016 | 0/0 | 3523 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0017 | 0/0 | 3523 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0018 | 0/0 | 3523 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0019 | 0/0 | 3523 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0020 | 0/0 | 3523 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0021 | 0/0 | 3523 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0022 | 0/0 | 3523 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0023 | 0/0 | 3523 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0024 | 0/0 | 3523 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0025 | 0/0 | 3523 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0026 | 0/0 | 3523 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0027 | 0/0 | 3523 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0028 | 0/0 | 3523 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0029 | 0/0 | 3523 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0030 | 0/0 | 3523 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0031 | 0/0 | 3523 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0032 | 0/0 | 3523 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0033 | 0/0 | 3523 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0034 | 0/0 | 3523 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0035 | 0/0 | 3523 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| t0036 | 0/0 | 3511 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0200 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| 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 | 1803 | 196 | 66 | 33 | 60 | 9 | 26 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0008 | 0/0 | 1803 | 3 | 0 | 3 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0012 | 0/0 | 1803 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0002c0002 | 0/0 | 1803 | 64 | 1 | 15 | 45 | 0 | 3 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0003c0003 | 0/0 | 1803 | 25 | 8 | 3 | 11 | 0 | 3 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0004c0005 | 0/0 | 1803 | 14 | 2 | 2 | 3 | 0 | 7 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0005c0004 | 0/0 | 1803 | 14 | 0 | 4 | 5 | 1 | 4 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0006c0006 | 0/0 | 1803 | 13 | 5 | 3 | 0 | 2 | 3 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0007c0007 | 0/0 | 1803 | 7 | 5 | 2 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0008c0009 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0009c0011 | 0/0 | 1803 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0010c0013 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0011c0010 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0012c0014 | 0/0 | 1803 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5325 | 142 | 41 | 16 | 54 | 6 | 23 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0001t0002 | 0/0 | 5325 | 4 | 2 | 1 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0001t0003 | 0/0 | 5325 | 22 | 2 | 14 | 0 | 3 | 3 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0001t0007 | 0/0 | 5325 | 5 | 4 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0001t0009 | 0/0 | 5325 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0001t0010 | 0/0 | 5325 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0001t0011 | 0/0 | 5325 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0001t0013 | 0/0 | 5325 | 2 | 0 | 0 | 2 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0001t0014 | 0/0 | 5325 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0001t0015 | 0/0 | 5325 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0001t0016 | 0/0 | 5325 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0001t0018 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0001t0020 | 0/0 | 5325 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0001t0025 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0001t0028 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0001t0029 | 0/0 | 5325 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0001t0030 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0001t0032 | 0/0 | 5325 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0001t0033 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0001t0034 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0001t0035 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0008t0001 | 0/0 | 5325 | 3 | 0 | 3 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0001c0012t0003 | 0/0 | 5325 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0002c0002t0002 | 0/0 | 5325 | 63 | 1 | 14 | 45 | 0 | 3 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0002c0002t0024 | 0/0 | 5325 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0003c0003t0002 | 0/0 | 5325 | 20 | 6 | 3 | 9 | 0 | 2 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0003c0003t0006 | 0/0 | 5325 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0003c0003t0021 | 0/0 | 5325 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0003c0003t0022 | 0/0 | 5325 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0003c0003t0027 | 0/0 | 5325 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0004c0005t0005 | 0/0 | 5313 | 12 | 0 | 2 | 3 | 0 | 7 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0004c0005t0012 | 0/0 | 5313 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0005c0004t0004 | 0/0 | 5313 | 13 | 0 | 3 | 5 | 1 | 4 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0005c0004t0036 | 0/0 | 5313 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0006c0006t0001 | 0/0 | 5325 | 12 | 4 | 3 | 0 | 2 | 3 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0006c0006t0026 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0007c0007t0006 | 0/0 | 5325 | 3 | 2 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0007c0007t0008 | 0/0 | 5325 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0007c0007t0019 | 0/0 | 5325 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0007c0007t0023 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0008c0009t0008 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0009c0011t0001 | 0/0 | 5325 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0010c0013t0031 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0011c0010t0017 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| a0012c0014t0003 | 0/0 | 5325 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | copy fasta | chr9 | 26951412 | 27071134 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0200 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0007g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0009g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0011g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0011g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0013g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0013g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0014g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0015g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0015g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0016g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0018g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0020g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0025g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0028g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0029g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0030g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0032g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0033g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0034g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0001t0035g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0008t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0008t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0008t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0001c0012t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0002c0002t0024g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0021g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0022g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0003c0003t0027g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0004c0005t0005g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0004c0005t0005g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0004c0005t0005g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0004c0005t0005g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0004c0005t0005g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0004c0005t0005g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0004c0005t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0004c0005t0005g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0004c0005t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0004c0005t0005g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0004c0005t0005g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0004c0005t0005g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0004c0005t0012g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0004c0005t0012g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0005c0004t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0005c0004t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0005c0004t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0005c0004t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0005c0004t0004g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0005c0004t0004g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0005c0004t0004g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0005c0004t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0005c0004t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0005c0004t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0005c0004t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0005c0004t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0005c0004t0004g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0005c0004t0036g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0006c0006t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0006c0006t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0006c0006t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0006c0006t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0006c0006t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0006c0006t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0006c0006t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0006c0006t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0006c0006t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0006c0006t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0006c0006t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0006c0006t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0006c0006t0026g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0007c0007t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0007c0007t0006g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0007c0007t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0007c0007t0008g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0007c0007t0008g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0007c0007t0019g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0007c0007t0023g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0008c0009t0008g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0009c0011t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0010c0013t0031g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0011c0010t0017g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| a0012c0014t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | GBR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0281 | EUR | GBR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | GBR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0295 | EUR | FIN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | FIN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0305 | EUR | FIN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00323 | hp2 | a0005 | c0004 | t0004 | g0020 | EUR | FIN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00408 | hp1 | a0003 | c0003 | t0002 | g0126 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0076 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0058 | EAS | CHS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0055 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00639 | hp2 | a0004 | c0005 | t0005 | g0310 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00733 | hp1 | a0007 | c0007 | t0006 | g0025 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00733 | hp2 | a0005 | c0004 | t0004 | g0023 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00735 | hp1 | a0001 | c0012 | t0003 | g0302 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00735 | hp2 | a0002 | c0002 | t0024 | g0320 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0283 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0297 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0273 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01069 | hp2 | a0006 | c0006 | t0001 | g0325 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01070 | hp2 | a0006 | c0006 | t0001 | g0334 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01074 | hp2 | a0001 | c0001 | t0007 | g0170 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0074 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0053 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0298 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01167 | hp2 | a0003 | c0003 | t0002 | g0111 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01169 | hp1 | a0003 | c0003 | t0002 | g0110 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0294 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0277 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01192 | hp2 | a0001 | c0008 | t0001 | g0168 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0073 | AMR | PUR | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0047 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01255 | hp2 | a0007 | c0007 | t0019 | g0118 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01256 | hp1 | a0004 | c0005 | t0005 | g0311 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0293 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01257 | hp1 | a0006 | c0006 | t0001 | g0332 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0296 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0071 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01358 | hp2 | a0001 | c0008 | t0001 | g0167 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0285 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01361 | hp2 | a0005 | c0004 | t0036 | g0028 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01496 | hp2 | a0005 | c0004 | t0004 | g0024 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01515 | hp1 | a0006 | c0006 | t0001 | g0330 | EUR | IBS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0246 | EUR | IBS | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01884 | hp1 | a0001 | c0001 | t0010 | g0034 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01891 | hp1 | a0001 | c0001 | t0030 | g0109 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01891 | hp2 | a0003 | c0003 | t0002 | g0324 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0288 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0057 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01934 | hp1 | a0005 | c0004 | t0004 | g0018 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0061 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0303 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0069 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0048 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01975 | hp2 | a0009 | c0011 | t0001 | g0235 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0056 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0291 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0271 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01993 | hp1 | a0001 | c0008 | t0001 | g0169 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01993 | hp2 | a0012 | c0014 | t0003 | g0282 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02055 | hp1 | a0003 | c0003 | t0006 | g0113 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02055 | hp2 | a0006 | c0006 | t0026 | g0206 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02056 | hp2 | a0005 | c0004 | t0004 | g0014 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02080 | hp1 | a0001 | c0001 | t0029 | g0157 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0070 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02145 | hp2 | a0006 | c0006 | t0001 | g0336 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CDX | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | CDX | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02258 | hp1 | a0006 | c0006 | t0001 | g0329 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02258 | hp2 | a0001 | c0001 | t0014 | g0001 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02273 | hp1 | a0001 | c0001 | t0016 | g0292 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0094 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0059 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02300 | hp1 | a0003 | c0003 | t0002 | g0100 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0286 | AMR | PEL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02451 | hp1 | a0001 | c0001 | t0011 | g0035 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02523 | hp2 | a0003 | c0003 | t0002 | g0038 | EAS | KHV | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02572 | hp2 | a0001 | c0001 | t0015 | g0130 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02615 | hp1 | a0007 | c0007 | t0008 | g0004 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02615 | hp2 | a0001 | c0001 | t0014 | g0001 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0173 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02630 | hp2 | a0007 | c0007 | t0006 | g0016 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02683 | hp1 | a0006 | c0006 | t0001 | g0328 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02683 | hp2 | a0003 | c0003 | t0002 | g0087 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0060 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02717 | hp1 | a0004 | c0005 | t0012 | g0341 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02717 | hp2 | a0006 | c0006 | t0001 | g0327 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02723 | hp2 | a0003 | c0003 | t0002 | g0321 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02735 | hp2 | a0004 | c0005 | t0005 | g0312 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02738 | hp2 | a0004 | c0005 | t0005 | g0317 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02886 | hp1 | a0003 | c0003 | t0002 | g0322 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02886 | hp2 | a0001 | c0001 | t0033 | g0104 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02895 | hp1 | a0003 | c0003 | t0006 | g0112 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0172 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0171 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02922 | hp1 | a0001 | c0001 | t0025 | g0175 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02970 | hp1 | a0001 | c0001 | t0010 | g0033 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0030 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03098 | hp1 | a0001 | c0001 | t0015 | g0131 | AFR | MSL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03130 | hp2 | a0003 | c0003 | t0002 | g0049 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03139 | hp1 | a0003 | c0003 | t0002 | g0323 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03209 | hp2 | a0007 | c0007 | t0023 | g0005 | AFR | MSL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03239 | hp1 | a0005 | c0004 | t0004 | g0019 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03239 | hp2 | a0004 | c0005 | t0005 | g0308 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03486 | hp1 | a0001 | c0001 | t0034 | g0140 | AFR | MSL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03486 | hp2 | a0001 | c0001 | t0035 | g0242 | AFR | MSL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0300 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03491 | hp2 | a0005 | c0004 | t0004 | g0017 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0299 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03540 | hp1 | a0001 | c0001 | t0018 | g0127 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0134 | AFR | MSL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03579 | hp2 | a0007 | c0007 | t0008 | g0003 | AFR | MSL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03654 | hp1 | a0004 | c0005 | t0005 | g0319 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0274 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | STU | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03688 | hp2 | a0003 | c0003 | t0022 | g0054 | SAS | STU | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03704 | hp2 | a0005 | c0004 | t0004 | g0275 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0075 | SAS | PJL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03834 | hp1 | a0004 | c0005 | t0005 | g0309 | SAS | BEB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03834 | hp2 | a0003 | c0003 | t0002 | g0037 | SAS | BEB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03927 | hp1 | a0006 | c0006 | t0001 | g0333 | SAS | BEB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0096 | SAS | BEB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | STU | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG04199 | hp1 | a0004 | c0005 | t0005 | g0313 | SAS | STU | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | STU | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG04228 | hp1 | a0006 | c0006 | t0001 | g0335 | SAS | STU | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | STU | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | CHB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | YRI | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | YRI | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18957 | hp1 | a0004 | c0005 | t0005 | g0318 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18959 | hp2 | a0001 | c0001 | t0013 | g0265 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18960 | hp1 | a0001 | c0001 | t0013 | g0266 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18960 | hp2 | a0005 | c0004 | t0004 | g0013 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18964 | hp1 | a0003 | c0003 | t0002 | g0067 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18965 | hp2 | a0004 | c0005 | t0005 | g0314 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18973 | hp1 | a0005 | c0004 | t0004 | g0027 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18973 | hp2 | a0003 | c0003 | t0002 | g0088 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18975 | hp1 | a0003 | c0003 | t0002 | g0090 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18984 | hp2 | a0005 | c0004 | t0004 | g0021 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18989 | hp2 | a0005 | c0004 | t0004 | g0015 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18994 | hp1 | a0004 | c0005 | t0005 | g0316 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18994 | hp2 | a0003 | c0003 | t0002 | g0092 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19010 | hp2 | a0003 | c0003 | t0002 | g0091 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19030 | hp1 | a0001 | c0001 | t0011 | g0032 | AFR | LWK | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19030 | hp2 | a0011 | c0010 | t0017 | g0114 | AFR | LWK | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | LWK | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19066 | hp1 | a0001 | c0001 | t0032 | g0224 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19068 | hp1 | a0003 | c0003 | t0002 | g0089 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19072 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19077 | hp1 | a0003 | c0003 | t0027 | g0098 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19081 | hp1 | a0001 | c0001 | t0020 | g0150 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19081 | hp2 | a0003 | c0003 | t0021 | g0099 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19090 | hp1 | a0003 | c0003 | t0002 | g0097 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19240 | hp1 | a0008 | c0009 | t0008 | g0002 | AFR | YRI | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA19240 | hp2 | a0004 | c0005 | t0012 | g0340 | AFR | YRI | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA20129 | hp1 | a0003 | c0003 | t0002 | g0042 | AFR | ASW | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ASW | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0244 | EUR | TSI | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA20752 | hp2 | a0006 | c0006 | t0001 | g0331 | EUR | TSI | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA20905 | hp1 | a0005 | c0004 | t0004 | g0022 | SAS | GIH | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA20905 | hp2 | a0004 | c0005 | t0005 | g0315 | SAS | GIH | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0280 | AMR | CLM | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02109 | hp2 | a0001 | c0001 | t0028 | g0301 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02559 | hp1 | a0006 | c0006 | t0001 | g0326 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG02559 | hp2 | a0010 | c0013 | t0031 | g0284 | AFR | ACB | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03471 | hp1 | a0001 | c0001 | t0009 | g0031 | AFR | MSL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0272 | AFR | USA | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| HG06807 | hp2 | a0007 | c0007 | t0006 | g0026 | AFR | USA | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | USA | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0276 | AFR | USA | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0201 | REF | REF | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0200 | REF | REF | IFT74_chr9_26951412_27071134 | IFT74 | chr9 | 26951412 | 27071134 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:26962001
|
C | T | 1 | a0012 | 1 | HG01993.hp2 | missense_variant | MODERATE | c.34C>T | p.Pro12Ser | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/20 | 158/5325 | 34/1803 | 12/600 | chr9 | 26962001 | ||
| chr9:26978159
|
G | A | 1 | a0008 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.152G>A | p.Arg51His | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/20 | 276/5325 | 152/1803 | 51/600 | chr9 | 26978159 | ||
| chr9:26978172
|
A | G | 1 | a0002 | 64 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(61): Show |
missense_variant | MODERATE | c.165A>G | p.Ile55Met | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/20 | 289/5325 | 165/1803 | 55/600 | chr9 | 26978172 | ||
| chr9:26978261
|
A | G | 2 | a0002a0003 | 89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
missense_variant&splice_region_variant | MODERATE | c.254A>G | p.Lys85Arg | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/20 | 378/5325 | 254/1803 | 85/600 | chr9 | 26978261 | ||
| chr9:26984279
|
A | G | 1 | a0006 | 13 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(10): Show |
missense_variant | MODERATE | c.328A>G | p.Thr110Ala | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 5/20 | 452/5325 | 328/1803 | 110/600 | chr9 | 26984279 | ||
| chr9:27009097
|
T | C | 1 | a0011 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.665T>C | p.Met222Thr | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/20 | 789/5325 | 665/1803 | 222/600 | chr9 | 27009097 | ||
| chr9:27009102
|
T | C | 3 | a0005a0007a0008 | 22 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(19): Show |
missense_variant | MODERATE | c.670T>C | p.Phe224Leu | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/20 | 794/5325 | 670/1803 | 224/600 | chr9 | 27009102 | ||
| chr9:27016910
|
A | G | 1 | a0010 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.793A>G | p.Ile265Val | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/20 | 917/5325 | 793/1803 | 265/600 | chr9 | 27016910 | ||
| chr9:27055618
|
G | A | 1 | a0009 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.1343G>A | p.Arg448His | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 17/20 | 1467/5325 | 1343/1803 | 448/600 | chr9 | 27055618 | ||
| chr9:27062723
|
C | T | 2 | a0004a0005 | 28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
missense_variant | MODERATE | c.1790C>T | p.Thr597Ile | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1914/5325 | 1790/1803 | 597/600 | chr9 | 27062723 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:26984311
|
A | G | 1 | a0001c0008 | 3 | HG01192.hp2 HG01358.hp2 HG01993.hp1 |
synonymous_variant | LOW | c.360A>G | p.Glu120Glu | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 5/20 | 484/5325 | 360/1803 | 120/600 | chr9 | 26984311 | ||
| chr9:27056378
|
C | T | 1 | a0001c0012 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.1542C>T | p.Ala514Ala | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/20 | 1666/5325 | 1542/1803 | 514/600 | chr9 | 27056378 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:26956434
|
C | T | 1 | a0005c0004t0036 | 1 | HG01361.hp2 | 5_prime_UTR_variant | MODIFIER | c.-102C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/20 | 5534 | chr9 | 26956434 | |||||
| chr9:26956487
|
G | A | 1 | a0001c0001t0016 | 1 | HG02273.hp1 | 5_prime_UTR_variant | MODIFIER | c.-49G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/20 | 5481 | chr9 | 26956487 | |||||
| chr9:26956505
|
G | A | 3 | a0001c0001t0018a0007c0007t0019a0011c0010t0017 | 3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-31G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/20 | 5463 | chr9 | 26956505 | |||||
| chr9:26961954
|
A | G | 1 | a0001c0001t0035 | 1 | HG03486.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-14A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/20 | chr9 | 26961954 | ||||||
| chr9:27062792
|
C | A | 1 | a0001c0001t0020 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*56C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 56 | chr9 | 27062792 | |||||
| chr9:27063177
|
T | C | 23 | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(20): Show | 138 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*441T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 441 | chr9 | 27063177 | |||||
| chr9:27063376
|
G | A | 1 | a0001c0001t0028 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*640G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 640 | chr9 | 27063376 | |||||
| chr9:27063510
|
G | A | 1 | a0001c0001t0029 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*774G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 774 | chr9 | 27063510 | |||||
| chr9:27063578
|
C | A | 1 | a0001c0001t0009 | 2 | HG03041.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*842C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 842 | chr9 | 27063578 | |||||
| chr9:27063666
|
T | C | 1 | a0001c0001t0013 | 2 | NA18959.hp2 NA18960.hp1 |
3_prime_UTR_variant | MODIFIER | c.*930T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 930 | chr9 | 27063666 | |||||
| chr9:27063697
|
A | G | 2 | a0007c0007t0008a0008c0009t0008 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*961A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 961 | chr9 | 27063697 | |||||
| chr9:27063736
|
C | T | 1 | a0001c0001t0034 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1000C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1000 | chr9 | 27063736 | |||||
| chr9:27063840
|
T | C | 1 | a0001c0001t0014 | 2 | HG02258.hp2 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1104T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1104 | chr9 | 27063840 | |||||
| chr9:27063847
|
G | A | 1 | a0001c0001t0007 | 5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1111G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1111 | chr9 | 27063847 | |||||
| chr9:27063857
|
C | T | 1 | a0001c0001t0033 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1121C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1121 | chr9 | 27063857 | |||||
| chr9:27063894
|
C | G | 1 | a0001c0001t0033 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1158C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1158 | chr9 | 27063894 | |||||
| chr9:27063998
|
C | T | 1 | a0001c0001t0015 | 2 | HG02572.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1262C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1262 | chr9 | 27063998 | |||||
| chr9:27063999
|
G | A | 1 | a0001c0001t0007 | 5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1263G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1263 | chr9 | 27063999 | |||||
| chr9:27064017
|
G | A | 2 | a0005c0004t0004a0005c0004t0036 | 14 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1281G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1281 | chr9 | 27064017 | |||||
| chr9:27064025
|
T | A | 1 | a0001c0001t0030 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1289T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1289 | chr9 | 27064025 | |||||
| chr9:27064055
|
A | G | 1 | a0003c0003t0027 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1319A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1319 | chr9 | 27064055 | |||||
| chr9:27064333
|
T | G | 2 | a0003c0003t0021a0003c0003t0027 | 2 | NA19077.hp1 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1597T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1597 | chr9 | 27064333 | |||||
| chr9:27064400
|
G | A | 6 | a0001c0001t0003a0001c0001t0016a0001c0001t0028others(3): Show | 27 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1664G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1664 | chr9 | 27064400 | |||||
| chr9:27064572
|
A | T | 1 | a0001c0001t0033 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1836A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1836 | chr9 | 27064572 | |||||
| chr9:27064608
|
A | G | 2 | a0003c0003t0006a0007c0007t0006 | 5 | HG00733.hp1 HG02055.hp1 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1872A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1872 | chr9 | 27064608 | |||||
| chr9:27064730
|
T | C | 1 | a0003c0003t0022 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1994T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1994 | chr9 | 27064730 | |||||
| chr9:27064732
|
A | G | 1 | a0004c0005t0012 | 2 | HG02717.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1996A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 1996 | chr9 | 27064732 | |||||
| chr9:27064757
|
G | A | 4 | a0001c0001t0009a0007c0007t0008a0007c0007t0023others(1): Show | 6 | HG02615.hp1 HG03041.hp2 HG03209.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2021G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2021 | chr9 | 27064757 | |||||
| chr9:27064792
|
CCCTTTTA others(5): Show |
C | 4 | a0004c0005t0005a0004c0005t0012a0005c0004t0004others(1): Show | 28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2059_*2070delTTTT others(8): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2059 | INFO_REALIGN_3_PRIME | chr9 | 27064792 | ||||
| chr9:27064840
|
T | A | 1 | a0002c0002t0024 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2104T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2104 | chr9 | 27064840 | |||||
| chr9:27064959
|
C | A | 1 | a0001c0001t0010 | 2 | HG01884.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2223C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2223 | chr9 | 27064959 | |||||
| chr9:27065169
|
T | A | 4 | a0001c0001t0009a0007c0007t0008a0007c0007t0023others(1): Show | 6 | HG02615.hp1 HG03041.hp2 HG03209.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2433T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2433 | chr9 | 27065169 | |||||
| chr9:27065194
|
G | A | 1 | a0001c0001t0025 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2458G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2458 | chr9 | 27065194 | |||||
| chr9:27065199
|
A | C | 1 | a0010c0013t0031 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2463A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2463 | chr9 | 27065199 | |||||
| chr9:27065297
|
C | T | 1 | a0001c0001t0018 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2561C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2561 | chr9 | 27065297 | |||||
| chr9:27065385
|
G | A | 2 | a0001c0001t0010a0001c0001t0011 | 4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2649G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2649 | chr9 | 27065385 | |||||
| chr9:27065494
|
G | C | 1 | a0001c0001t0011 | 2 | HG02451.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2758G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2758 | chr9 | 27065494 | |||||
| chr9:27065656
|
T | G | 1 | a0001c0001t0032 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2920T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 2920 | chr9 | 27065656 | |||||
| chr9:27065781
|
A | G | 1 | a0006c0006t0026 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3045A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 3045 | chr9 | 27065781 | |||||
| chr9:27066072
|
T | C | 4 | a0004c0005t0005a0004c0005t0012a0005c0004t0004others(1): Show | 28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3336T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 20/20 | 3336 | chr9 | 27066072 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:26956551
|
C | T | 2 | a0004c0005t0012g0340a0004c0005t0012g0341 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-20+35C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956551 | ||||||
| chr9:26956563
|
G | C | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-20+47G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956563 | ||||||
| chr9:26956580
|
A | C | 15 | a0001c0001t0001g0337a0001c0001t0001g0338a0001c0001t0001g0339others(12): Show | 15 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+64A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956580 | ||||||
| chr9:26956655
|
C | T | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+139C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956655 | ||||||
| chr9:26956664
|
A | T | 1 | a0002c0002t0024g0320 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-20+148A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956664 | ||||||
| chr9:26956665
|
C | T | 14 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(11): Show | 14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+149C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956665 | ||||||
| chr9:26956704
|
C | G | 1 | a0001c0001t0001g0307 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-20+188C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956704 | ||||||
| chr9:26956725
|
AC | A | 14 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(11): Show | 14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+215delC | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 26956725 | |||||
| chr9:26956761
|
G | A | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-20+245G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956761 | ||||||
| chr9:26956770
|
G | A | 161 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(158): Show | 161 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.-20+254G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956770 | ||||||
| chr9:26956807
|
T | C | 7 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(4): Show | 7 | HG00621.hp1 NA18959.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+291T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956807 | ||||||
| chr9:26956834
|
T | C | 16 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(13): Show | 16 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.-20+318T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956834 | ||||||
| chr9:26956860
|
C | T | 1 | a0005c0004t0036g0028 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-20+344C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956860 | ||||||
| chr9:26956870
|
C | G | 105 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(102): Show | 105 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.-20+354C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956870 | ||||||
| chr9:26956881
|
T | C | 2 | a0001c0001t0001g0203a0001c0001t0001g0307 | 2 | HG00609.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-20+365T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956881 | ||||||
| chr9:26956906
|
T | A | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-20+390T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26956906 | ||||||
| chr9:26957093
|
A | G | 1 | a0001c0001t0001g0306 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-20+577A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26957093 | ||||||
| chr9:26957117
|
C | G | 1 | a0005c0004t0004g0027 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-20+601C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26957117 | ||||||
| chr9:26957152
|
C | A | 20 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(17): Show | 20 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-20+636C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26957152 | ||||||
| chr9:26957235
|
T | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG03490.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-20+719T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26957235 | ||||||
| chr9:26957700
|
A | C | 2 | a0001c0001t0015g0130a0001c0001t0015g0131 | 2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-20+1184A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26957700 | ||||||
| chr9:26957799
|
C | CT | 8 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0018g0127others(5): Show | 8 | HG00408.hp1 HG01496.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+1295dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 26957799 | |||||
| chr9:26957863
|
G | A | 1 | a0002c0002t0002g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-20+1347G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26957863 | ||||||
| chr9:26957913
|
A | C | 194 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(191): Show | 194 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-20+1397A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26957913 | ||||||
| chr9:26958050
|
G | A | 16 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(13): Show | 16 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.-20+1534G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26958050 | ||||||
| chr9:26958246
|
G | A | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-20+1730G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26958246 | ||||||
| chr9:26958371
|
C | T | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-20+1855C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26958371 | ||||||
| chr9:26958441
|
C | G | 16 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(13): Show | 16 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.-20+1925C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26958441 | ||||||
| chr9:26958457
|
C | G | 4 | a0002c0002t0002g0122a0002c0002t0002g0123a0002c0002t0002g0124others(1): Show | 4 | NA18991.hp2 NA19002.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+1941C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26958457 | ||||||
| chr9:26958659
|
T | A | 1 | a0005c0004t0004g0013 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-20+2143T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26958659 | ||||||
| chr9:26958670
|
T | A | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-20+2154T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26958670 | ||||||
| chr9:26958730
|
G | C | 81 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(78): Show | 81 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.-20+2214G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26958730 | ||||||
| chr9:26958764
|
G | A | 1 | a0002c0002t0002g0036 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-20+2248G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26958764 | ||||||
| chr9:26958924
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-20+2408G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26958924 | ||||||
| chr9:26959089
|
T | TTTG | 97 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(94): Show | 97 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.-20+2606_-20+2608d others(5): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 26959089 | |||||
| chr9:26959089
|
T | TTTGTTG | 7 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0007g0134others(4): Show | 7 | HG02523.hp2 HG02723.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+2603_-20+2608d others(8): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 26959089 | |||||
| chr9:26959089
|
T | TTTGTTGT others(2): Show |
13 | a0001c0001t0015g0130a0001c0001t0015g0131a0004c0005t0005g0308others(10): Show | 13 | HG00639.hp2 HG01256.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-20+2600_-20+2608d others(11): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 26959089 | |||||
| chr9:26959089
|
TTTG | T | 26 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(23): Show | 26 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.-20+2606_-20+2608d others(5): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 26959089 | |||||
| chr9:26959089
|
TTTGTTG | T | 10 | a0001c0001t0001g0201a0001c0001t0001g0263a0001c0001t0001g0264others(7): Show | 10 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20+2603_-20+2608d others(8): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 26959089 | |||||
| chr9:26959139
|
C | T | 89 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(86): Show | 89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.-20+2623C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26959139 | ||||||
| chr9:26959159
|
A | T | 89 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(86): Show | 89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.-20+2643A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26959159 | ||||||
| chr9:26959181
|
T | C | 14 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(11): Show | 14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+2665T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26959181 | ||||||
| chr9:26959269
|
C | T | 1 | a0005c0004t0036g0028 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-19-2680C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26959269 | ||||||
| chr9:26959303
|
G | A | 1 | a0006c0006t0026g0206 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-19-2646G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26959303 | ||||||
| chr9:26959383
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-19-2566G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26959383 | ||||||
| chr9:26959400
|
C | T | 2 | a0003c0003t0006g0112a0003c0003t0006g0113 | 2 | HG02055.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-19-2549C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26959400 | ||||||
| chr9:26959916
|
A | G | 14 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(11): Show | 14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.-19-2033A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26959916 | ||||||
| chr9:26959988
|
G | C | 1 | a0001c0001t0001g0208 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-19-1961G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26959988 | ||||||
| chr9:26960087
|
A | G | 157 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(154): Show | 157 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-19-1862A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26960087 | ||||||
| chr9:26960122
|
T | G | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-19-1827T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26960122 | ||||||
| chr9:26960228
|
A | T | 1 | a0001c0001t0001g0205 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-19-1721A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26960228 | ||||||
| chr9:26960290
|
G | C | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-19-1659G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26960290 | ||||||
| chr9:26960320
|
T | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG01496.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-19-1629T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26960320 | ||||||
| chr9:26960405
|
A | G | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-19-1544A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26960405 | ||||||
| chr9:26960525
|
T | G | 6 | a0001c0001t0003g0272a0001c0001t0003g0273a0001c0001t0003g0274others(3): Show | 6 | HG01069.hp1 HG01175.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-1424T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26960525 | ||||||
| chr9:26960777
|
G | A | 340 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(337): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.-19-1172G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26960777 | ||||||
| chr9:26961018
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-19-931C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961018 | ||||||
| chr9:26961051
|
G | T | 1 | a0001c0001t0001g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-19-898G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961051 | ||||||
| chr9:26961083
|
G | GT | 36 | a0001c0001t0001g0117a0001c0001t0001g0195a0001c0001t0001g0196others(33): Show | 36 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.-19-848dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 26961083 | |||||
| chr9:26961083
|
G | GTT | 16 | a0001c0001t0009g0031a0001c0001t0010g0033a0001c0001t0010g0034others(13): Show | 16 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19-849_-19-848dup others(2): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 26961083 | |||||
| chr9:26961108
|
G | A | 75 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0203others(72): Show | 75 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.-19-841G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961108 | ||||||
| chr9:26961109
|
G | T | 84 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(81): Show | 84 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.-19-840G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961109 | ||||||
| chr9:26961125
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-19-824G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961125 | ||||||
| chr9:26961225
|
G | C | 84 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(81): Show | 84 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.-19-724G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961225 | ||||||
| chr9:26961257
|
A | AT | 14 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(11): Show | 14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.-19-686dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 26961257 | |||||
| chr9:26961306
|
G | T | 1 | a0003c0003t0002g0038 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-19-643G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961306 | ||||||
| chr9:26961312
|
C | G | 332 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(329): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-19-637C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961312 | ||||||
| chr9:26961435
|
C | A | 20 | a0001c0001t0001g0207a0001c0001t0001g0209a0001c0001t0001g0210others(17): Show | 20 | HG00423.hp2 HG02129.hp1 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.-19-514C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961435 | ||||||
| chr9:26961476
|
T | C | 1 | a0003c0003t0027g0098 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-19-473T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961476 | ||||||
| chr9:26961575
|
C | G | 1 | a0007c0007t0019g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-19-374C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961575 | ||||||
| chr9:26961622
|
A | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-19-327A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961622 | ||||||
| chr9:26961749
|
G | T | 2 | a0001c0001t0018g0127a0007c0007t0019g0118 | 2 | HG01255.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-19-200G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961749 | ||||||
| chr9:26961838
|
C | T | 15 | a0001c0001t0001g0337a0001c0001t0001g0338a0001c0001t0001g0339others(12): Show | 15 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19-111C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961838 | ||||||
| chr9:26961893
|
T | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG01496.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-19-56T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 1/19 | chr9 | 26961893 | ||||||
| chr9:26962172
|
C | A | 93 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(90): Show | 93 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.120+85C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26962172 | ||||||
| chr9:26962407
|
C | A | 20 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(17): Show | 20 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.120+320C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26962407 | ||||||
| chr9:26962462
|
T | G | 1 | a0002c0002t0002g0039 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.120+375T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26962462 | ||||||
| chr9:26962490
|
A | G | 34 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(31): Show | 34 | HG00323.hp2 HG00639.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.120+403A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26962490 | ||||||
| chr9:26962671
|
G | C | 1 | a0004c0005t0005g0308 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.120+584G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26962671 | ||||||
| chr9:26962771
|
A | G | 34 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(31): Show | 34 | HG00323.hp2 HG00639.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.120+684A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26962771 | ||||||
| chr9:26962845
|
A | T | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.120+758A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26962845 | ||||||
| chr9:26962872
|
T | C | 15 | a0001c0001t0001g0337a0001c0001t0001g0338a0001c0001t0001g0339others(12): Show | 15 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.120+785T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26962872 | ||||||
| chr9:26962926
|
A | AT | 14 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(11): Show | 14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.120+852dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26962926 | |||||
| chr9:26962926
|
AT | A | 62 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0119others(59): Show | 62 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.120+852delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26962926 | |||||
| chr9:26962926
|
ATT | A | 13 | a0001c0001t0001g0149a0001c0001t0001g0199a0006c0006t0001g0325others(10): Show | 13 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.120+851_120+852del others(2): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26962926 | |||||
| chr9:26962930
|
T | TTTTC | 86 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(83): Show | 86 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.120+846_120+847ins others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26962930 | |||||
| chr9:26962930
|
T | TTTTTC | 19 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(16): Show | 19 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.120+847_120+848ins others(5): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26962930 | |||||
| chr9:26963090
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.120+1003C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963090 | ||||||
| chr9:26963113
|
C | G | 1 | a0001c0001t0025g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.120+1026C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963113 | ||||||
| chr9:26963113
|
C | T | 1 | a0002c0002t0002g0011 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.120+1026C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963113 | ||||||
| chr9:26963123
|
A | G | 1 | a0001c0001t0032g0224 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.120+1036A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963123 | ||||||
| chr9:26963131
|
C | A | 88 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(85): Show | 88 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.120+1044C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963131 | ||||||
| chr9:26963204
|
C | T | 1 | a0006c0006t0026g0206 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.120+1117C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963204 | ||||||
| chr9:26963229
|
G | A | 164 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(161): Show | 164 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(161): Show |
intron_variant | MODIFIER | c.120+1142G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963229 | ||||||
| chr9:26963303
|
A | G | 1 | a0002c0002t0002g0094 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.120+1216A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963303 | ||||||
| chr9:26963304
|
T | C | 1 | a0002c0002t0002g0094 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.120+1217T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963304 | ||||||
| chr9:26963407
|
C | T | 89 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(86): Show | 89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.120+1320C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963407 | ||||||
| chr9:26963618
|
CTGT | C | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.120+1536_120+1538d others(5): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26963618 | |||||
| chr9:26963670
|
G | A | 108 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(105): Show | 108 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.120+1583G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963670 | ||||||
| chr9:26963688
|
C | T | 33 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(30): Show | 33 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.120+1601C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963688 | ||||||
| chr9:26963715
|
A | G | 1 | a0007c0007t0019g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.120+1628A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963715 | ||||||
| chr9:26963742
|
C | T | 1 | a0002c0002t0002g0093 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.120+1655C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963742 | ||||||
| chr9:26963752
|
G | A | 1 | a0006c0006t0001g0325 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.120+1665G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963752 | ||||||
| chr9:26963763
|
G | A | 4 | a0001c0001t0010g0033a0001c0001t0010g0034a0001c0001t0011g0032others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+1676G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963763 | ||||||
| chr9:26963772
|
G | T | 4 | a0001c0001t0010g0033a0001c0001t0010g0034a0001c0001t0011g0032others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+1685G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963772 | ||||||
| chr9:26963776
|
G | C | 4 | a0001c0001t0010g0033a0001c0001t0010g0034a0001c0001t0011g0032others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+1689G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963776 | ||||||
| chr9:26963844
|
A | G | 16 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(13): Show | 16 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.120+1757A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963844 | ||||||
| chr9:26963916
|
G | C | 3 | a0001c0001t0011g0032a0001c0001t0011g0035a0007c0007t0023g0005 | 3 | HG02451.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.120+1829G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963916 | ||||||
| chr9:26963969
|
G | T | 2 | a0001c0001t0001g0223a0003c0003t0006g0112 | 2 | HG02895.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.120+1882G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26963969 | ||||||
| chr9:26964000
|
G | A | 14 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(11): Show | 14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.120+1913G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964000 | ||||||
| chr9:26964011
|
T | C | 89 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(86): Show | 89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.120+1924T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964011 | ||||||
| chr9:26964079
|
G | C | 84 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(81): Show | 84 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.120+1992G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964079 | ||||||
| chr9:26964104
|
G | A | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.120+2017G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964104 | ||||||
| chr9:26964110
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.120+2023G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964110 | ||||||
| chr9:26964178
|
A | G | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.120+2091A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964178 | ||||||
| chr9:26964211
|
T | G | 2 | a0003c0003t0002g0110a0003c0003t0002g0111 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.120+2124T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964211 | ||||||
| chr9:26964230
|
C | G | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.120+2143C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964230 | ||||||
| chr9:26964285
|
GT | G | 88 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(85): Show | 88 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.120+2200delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26964285 | |||||
| chr9:26964439
|
C | T | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.120+2352C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964439 | ||||||
| chr9:26964582
|
C | T | 8 | a0003c0003t0002g0038a0003c0003t0002g0088a0003c0003t0002g0089others(5): Show | 8 | HG00408.hp1 HG02523.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.120+2495C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964582 | ||||||
| chr9:26964617
|
GT | G | 6 | a0001c0001t0009g0030a0001c0001t0009g0031a0001c0001t0010g0033others(3): Show | 6 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.120+2532delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26964617 | |||||
| chr9:26964739
|
C | T | 3 | a0001c0001t0018g0127a0007c0007t0019g0118a0011c0010t0017g0114 | 3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.120+2652C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964739 | ||||||
| chr9:26964801
|
T | C | 89 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(86): Show | 89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.120+2714T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26964801 | ||||||
| chr9:26965356
|
T | G | 1 | a0001c0001t0033g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.120+3269T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26965356 | ||||||
| chr9:26965399
|
G | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG01496.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.120+3312G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26965399 | ||||||
| chr9:26965469
|
G | C | 13 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(10): Show | 13 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.120+3382G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26965469 | ||||||
| chr9:26965524
|
G | A | 1 | a0001c0001t0020g0150 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.120+3437G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26965524 | ||||||
| chr9:26965683
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.120+3596A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26965683 | ||||||
| chr9:26965687
|
A | G | 4 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+3600A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26965687 | ||||||
| chr9:26965707
|
G | C | 1 | a0001c0001t0033g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.120+3620G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26965707 | ||||||
| chr9:26965810
|
T | C | 28 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(25): Show | 28 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.120+3723T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26965810 | ||||||
| chr9:26965855
|
C | G | 3 | a0001c0001t0018g0127a0007c0007t0019g0118a0011c0010t0017g0114 | 3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.120+3768C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26965855 | ||||||
| chr9:26966022
|
G | T | 1 | a0002c0002t0002g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.120+3935G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966022 | ||||||
| chr9:26966067
|
C | T | 33 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(30): Show | 33 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.120+3980C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966067 | ||||||
| chr9:26966207
|
A | G | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.120+4120A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966207 | ||||||
| chr9:26966301
|
A | G | 16 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(13): Show | 16 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.120+4214A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966301 | ||||||
| chr9:26966438
|
C | T | 1 | a0001c0001t0010g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.120+4351C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966438 | ||||||
| chr9:26966445
|
G | A | 156 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(153): Show | 156 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.120+4358G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966445 | ||||||
| chr9:26966476
|
T | C | 16 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(13): Show | 16 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.120+4389T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966476 | ||||||
| chr9:26966554
|
A | T | 109 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(106): Show | 109 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.120+4467A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966554 | ||||||
| chr9:26966561
|
A | G | 15 | a0001c0001t0001g0337a0001c0001t0001g0338a0001c0001t0001g0339others(12): Show | 15 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.120+4474A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966561 | ||||||
| chr9:26966722
|
G | C | 1 | a0002c0002t0002g0040 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.120+4635G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966722 | ||||||
| chr9:26966761
|
G | C | 1 | a0001c0001t0001g0225 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.120+4674G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966761 | ||||||
| chr9:26966901
|
A | G | 1 | a0003c0003t0002g0087 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.120+4814A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26966901 | ||||||
| chr9:26967063
|
A | G | 1 | a0001c0001t0033g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.120+4976A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26967063 | ||||||
| chr9:26967142
|
T | A | 1 | a0002c0002t0002g0041 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.120+5055T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26967142 | ||||||
| chr9:26967375
|
C | A | 1 | a0001c0001t0003g0272 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.120+5288C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26967375 | ||||||
| chr9:26967381
|
T | A | 1 | a0001c0001t0001g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.120+5294T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26967381 | ||||||
| chr9:26967404
|
G | A | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+5317G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26967404 | ||||||
| chr9:26967478
|
A | G | 331 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(328): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.120+5391A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26967478 | ||||||
| chr9:26967787
|
G | A | 89 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(86): Show | 89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.120+5700G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26967787 | ||||||
| chr9:26967825
|
G | C | 2 | a0004c0005t0005g0308a0004c0005t0005g0309 | 2 | HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.120+5738G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26967825 | ||||||
| chr9:26967884
|
T | C | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.120+5797T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26967884 | ||||||
| chr9:26967977
|
C | T | 5 | a0001c0001t0007g0134a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+5890C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26967977 | ||||||
| chr9:26968025
|
G | T | 1 | a0001c0001t0001g0129 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.120+5938G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968025 | ||||||
| chr9:26968066
|
CT | C | 65 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(62): Show | 65 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.120+5996delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26968066 | |||||
| chr9:26968066
|
CTT | C | 85 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(82): Show | 85 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.120+5995_120+5996d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26968066 | |||||
| chr9:26968077
|
T | A | 33 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(30): Show | 33 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.120+5990T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968077 | ||||||
| chr9:26968122
|
G | A | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.120+6035G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968122 | ||||||
| chr9:26968139
|
A | G | 1 | a0001c0001t0001g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.120+6052A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968139 | ||||||
| chr9:26968256
|
TA | T | 15 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(12): Show | 15 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.120+6178delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26968256 | |||||
| chr9:26968265
|
AT | A | 147 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(144): Show | 147 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.120+6192delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26968265 | |||||
| chr9:26968286
|
T | G | 331 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(328): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.120+6199T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968286 | ||||||
| chr9:26968324
|
C | CT | 3 | a0001c0001t0018g0127a0007c0007t0019g0118a0011c0010t0017g0114 | 3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.120+6237_120+6238i others(3): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968324 | ||||||
| chr9:26968326
|
A | C | 3 | a0001c0001t0018g0127a0007c0007t0019g0118a0011c0010t0017g0114 | 3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.120+6239A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968326 | ||||||
| chr9:26968346
|
C | T | 15 | a0002c0002t0002g0076a0002c0002t0002g0077a0002c0002t0002g0078others(12): Show | 15 | HG00558.hp2 HG00609.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.120+6259C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968346 | ||||||
| chr9:26968364
|
C | T | 1 | a0003c0003t0002g0100 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.120+6277C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968364 | ||||||
| chr9:26968365
|
G | A | 1 | a0003c0003t0002g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.120+6278G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968365 | ||||||
| chr9:26968410
|
T | C | 109 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(106): Show | 109 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.120+6323T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968410 | ||||||
| chr9:26968432
|
T | G | 23 | a0001c0001t0001g0149a0001c0001t0001g0152a0001c0001t0001g0176others(20): Show | 23 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.120+6345T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968432 | ||||||
| chr9:26968434
|
A | G | 2 | a0001c0001t0003g0299a0001c0001t0003g0300 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.120+6347A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968434 | ||||||
| chr9:26968517
|
C | T | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+6430C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968517 | ||||||
| chr9:26968672
|
T | C | 89 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(86): Show | 89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.120+6585T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968672 | ||||||
| chr9:26968700
|
T | C | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.120+6613T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968700 | ||||||
| chr9:26968802
|
C | CT | 29 | a0001c0001t0001g0287a0001c0001t0001g0290a0001c0001t0001g0304others(26): Show | 29 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.120+6722dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26968802 | |||||
| chr9:26968833
|
T | G | 1 | a0001c0001t0011g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.120+6746T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968833 | ||||||
| chr9:26968836
|
T | C | 15 | a0001c0001t0001g0337a0001c0001t0001g0338a0001c0001t0001g0339others(12): Show | 15 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.120+6749T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968836 | ||||||
| chr9:26968862
|
C | G | 3 | a0001c0001t0018g0127a0007c0007t0019g0118a0011c0010t0017g0114 | 3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.120+6775C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26968862 | ||||||
| chr9:26968890
|
AT | A | 161 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(158): Show | 161 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.120+6811delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26968890 | |||||
| chr9:26969115
|
G | T | 7 | a0001c0001t0003g0293a0001c0001t0003g0294a0001c0001t0003g0295others(4): Show | 7 | HG00280.hp1 HG00323.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+7028G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969115 | ||||||
| chr9:26969179
|
C | G | 1 | a0001c0001t0003g0298 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.120+7092C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969179 | ||||||
| chr9:26969182
|
G | A | 28 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(25): Show | 28 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.120+7095G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969182 | ||||||
| chr9:26969212
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.120+7125C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969212 | ||||||
| chr9:26969253
|
T | C | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.120+7166T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969253 | ||||||
| chr9:26969324
|
A | C | 13 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(10): Show | 13 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.120+7237A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969324 | ||||||
| chr9:26969351
|
C | T | 3 | a0001c0001t0018g0127a0007c0007t0019g0118a0011c0010t0017g0114 | 3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.120+7264C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969351 | ||||||
| chr9:26969381
|
T | C | 89 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(86): Show | 89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.120+7294T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969381 | ||||||
| chr9:26969459
|
T | A | 165 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(162): Show | 165 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.120+7372T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969459 | ||||||
| chr9:26969512
|
T | A | 89 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(86): Show | 89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.120+7425T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969512 | ||||||
| chr9:26969565
|
T | A | 1 | a0001c0001t0001g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.120+7478T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969565 | ||||||
| chr9:26969771
|
G | A | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+7684G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969771 | ||||||
| chr9:26969787
|
A | G | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.120+7700A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969787 | ||||||
| chr9:26969938
|
C | T | 89 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(86): Show | 89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.120+7851C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969938 | ||||||
| chr9:26969939
|
G | A | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.120+7852G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969939 | ||||||
| chr9:26969993
|
C | T | 20 | a0001c0001t0001g0207a0001c0001t0001g0209a0001c0001t0001g0210others(17): Show | 20 | HG00423.hp2 HG02129.hp1 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.120+7906C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26969993 | ||||||
| chr9:26970059
|
C | A | 2 | a0006c0006t0001g0326a0006c0006t0001g0327 | 2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.120+7972C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26970059 | ||||||
| chr9:26970129
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.121-7999C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26970129 | ||||||
| chr9:26970364
|
T | C | 3 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026 | 3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.121-7764T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26970364 | ||||||
| chr9:26970386
|
A | T | 109 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(106): Show | 109 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.121-7742A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26970386 | ||||||
| chr9:26970561
|
A | G | 3 | a0001c0008t0001g0167a0001c0008t0001g0168a0001c0008t0001g0169 | 3 | HG01192.hp2 HG01358.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.121-7567A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26970561 | ||||||
| chr9:26970656
|
T | C | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-7472T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26970656 | ||||||
| chr9:26970819
|
A | G | 1 | a0006c0006t0001g0335 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.121-7309A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26970819 | ||||||
| chr9:26970835
|
G | A | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-7293G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26970835 | ||||||
| chr9:26970949
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.121-7179G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26970949 | ||||||
| chr9:26970965
|
A | G | 1 | a0001c0001t0028g0301 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.121-7163A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26970965 | ||||||
| chr9:26971121
|
C | T | 3 | a0001c0001t0018g0127a0007c0007t0019g0118a0011c0010t0017g0114 | 3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.121-7007C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971121 | ||||||
| chr9:26971128
|
G | A | 2 | a0003c0003t0006g0112a0003c0003t0006g0113 | 2 | HG02055.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.121-7000G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971128 | ||||||
| chr9:26971300
|
G | C | 1 | a0003c0003t0002g0088 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.121-6828G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971300 | ||||||
| chr9:26971366
|
A | G | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-6762A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971366 | ||||||
| chr9:26971438
|
C | T | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG02895.hp2 HG02897.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121-6690C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971438 | ||||||
| chr9:26971558
|
G | T | 4 | a0007c0007t0008g0003a0007c0007t0008g0004a0007c0007t0023g0005others(1): Show | 4 | HG02615.hp1 HG03209.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-6570G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971558 | ||||||
| chr9:26971580
|
C | T | 1 | a0002c0002t0002g0075 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.121-6548C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971580 | ||||||
| chr9:26971634
|
A | G | 1 | a0010c0013t0031g0284 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.121-6494A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971634 | ||||||
| chr9:26971816
|
T | C | 2 | a0003c0003t0006g0112a0003c0003t0006g0113 | 2 | HG02055.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.121-6312T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971816 | ||||||
| chr9:26971854
|
A | C | 1 | a0006c0006t0001g0334 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.121-6274A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971854 | ||||||
| chr9:26971898
|
A | G | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.121-6230A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26971898 | ||||||
| chr9:26972016
|
C | G | 1 | a0006c0006t0001g0333 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.121-6112C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26972016 | ||||||
| chr9:26972256
|
C | G | 1 | a0001c0001t0001g0178 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.121-5872C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26972256 | ||||||
| chr9:26972347
|
A | G | 2 | a0001c0001t0015g0130a0001c0001t0015g0131 | 2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.121-5781A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26972347 | ||||||
| chr9:26972432
|
G | A | 1 | a0002c0002t0002g0043 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.121-5696G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26972432 | ||||||
| chr9:26972502
|
G | C | 1 | a0009c0011t0001g0235 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.121-5626G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26972502 | ||||||
| chr9:26972558
|
G | C | 23 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(20): Show | 23 | HG00323.hp2 HG00639.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.121-5570G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26972558 | ||||||
| chr9:26973112
|
G | A | 89 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(86): Show | 89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.121-5016G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973112 | ||||||
| chr9:26973121
|
C | T | 3 | a0001c0001t0018g0127a0007c0007t0019g0118a0011c0010t0017g0114 | 3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.121-5007C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973121 | ||||||
| chr9:26973168
|
A | T | 1 | a0002c0002t0002g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.121-4960A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973168 | ||||||
| chr9:26973186
|
G | C | 1 | a0001c0001t0001g0240 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.121-4942G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973186 | ||||||
| chr9:26973210
|
C | T | 16 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(13): Show | 16 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.121-4918C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973210 | ||||||
| chr9:26973362
|
A | G | 89 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(86): Show | 89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.121-4766A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973362 | ||||||
| chr9:26973527
|
G | A | 14 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(11): Show | 14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.121-4601G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973527 | ||||||
| chr9:26973635
|
C | A | 14 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(11): Show | 14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.121-4493C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973635 | ||||||
| chr9:26973655
|
G | A | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-4473G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973655 | ||||||
| chr9:26973677
|
A | T | 1 | a0002c0002t0002g0093 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.121-4451A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973677 | ||||||
| chr9:26973787
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0020g0150 | 2 | HG02056.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.121-4341G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26973787 | ||||||
| chr9:26974056
|
C | T | 2 | a0003c0003t0021g0099a0003c0003t0027g0098 | 2 | NA19077.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.121-4072C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26974056 | ||||||
| chr9:26974099
|
A | C | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-4029A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26974099 | ||||||
| chr9:26974123
|
C | T | 2 | a0001c0001t0001g0257a0001c0001t0001g0307 | 2 | NA18969.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.121-4005C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26974123 | ||||||
| chr9:26974124
|
G | A | 10 | a0001c0001t0003g0285a0001c0001t0003g0286a0001c0001t0003g0293others(7): Show | 10 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.121-4004G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26974124 | ||||||
| chr9:26974247
|
G | T | 233 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(230): Show | 234 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.121-3881G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26974247 | ||||||
| chr9:26974419
|
A | G | 2 | a0004c0005t0012g0340a0004c0005t0012g0341 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.121-3709A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26974419 | ||||||
| chr9:26974524
|
T | G | 1 | a0001c0001t0001g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.121-3604T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26974524 | ||||||
| chr9:26974693
|
C | T | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-3435C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26974693 | ||||||
| chr9:26974839
|
A | C | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.121-3289A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26974839 | ||||||
| chr9:26974862
|
C | A | 6 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0001g0243others(3): Show | 6 | HG01884.hp2 HG02647.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.121-3266C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26974862 | ||||||
| chr9:26975079
|
T | TA | 88 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(85): Show | 88 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.121-3048dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 26975079 | |||||
| chr9:26975134
|
G | A | 88 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(85): Show | 88 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.121-2994G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975134 | ||||||
| chr9:26975151
|
G | T | 90 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(87): Show | 90 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.121-2977G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975151 | ||||||
| chr9:26975280
|
T | G | 1 | a0006c0006t0001g0335 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.121-2848T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975280 | ||||||
| chr9:26975285
|
A | G | 6 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0001g0243others(3): Show | 6 | HG01884.hp2 HG02647.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.121-2843A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975285 | ||||||
| chr9:26975426
|
A | T | 17 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(14): Show | 17 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.121-2702A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975426 | ||||||
| chr9:26975439
|
G | A | 3 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026 | 3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.121-2689G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975439 | ||||||
| chr9:26975440
|
G | A | 1 | a0006c0006t0026g0206 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.121-2688G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975440 | ||||||
| chr9:26975469
|
A | G | 13 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(10): Show | 13 | HG01192.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.121-2659A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975469 | ||||||
| chr9:26975520
|
C | T | 1 | a0001c0001t0003g0286 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.121-2608C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975520 | ||||||
| chr9:26975570
|
G | A | 89 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(86): Show | 89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.121-2558G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975570 | ||||||
| chr9:26975599
|
C | T | 81 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(78): Show | 81 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.121-2529C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975599 | ||||||
| chr9:26975647
|
T | C | 12 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(9): Show | 12 | HG00639.hp2 HG01256.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.121-2481T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975647 | ||||||
| chr9:26975657
|
C | T | 12 | a0006c0006t0001g0325a0006c0006t0001g0326a0006c0006t0001g0327others(9): Show | 12 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.121-2471C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975657 | ||||||
| chr9:26975951
|
T | G | 3 | a0001c0001t0018g0127a0007c0007t0019g0118a0011c0010t0017g0114 | 3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.121-2177T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26975951 | ||||||
| chr9:26976045
|
C | T | 1 | a0001c0001t0016g0292 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.121-2083C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976045 | ||||||
| chr9:26976088
|
C | T | 4 | a0001c0001t0010g0033a0001c0001t0010g0034a0001c0001t0011g0032others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-2040C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976088 | ||||||
| chr9:26976257
|
G | C | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-1871G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976257 | ||||||
| chr9:26976296
|
G | A | 6 | a0003c0003t0002g0322a0003c0003t0002g0323a0005c0004t0004g0017others(3): Show | 6 | HG00733.hp2 HG01934.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.121-1832G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976296 | ||||||
| chr9:26976298
|
A | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0231a0001c0001t0001g0306 | 3 | HG01243.hp1 HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.121-1830A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976298 | ||||||
| chr9:26976446
|
C | T | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-1682C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976446 | ||||||
| chr9:26976492
|
A | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0231a0001c0001t0001g0306 | 3 | HG01243.hp1 HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.121-1636A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976492 | ||||||
| chr9:26976679
|
A | C | 1 | a0003c0003t0002g0100 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.121-1449A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976679 | ||||||
| chr9:26976879
|
T | C | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.121-1249T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976879 | ||||||
| chr9:26976881
|
G | T | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.121-1247G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976881 | ||||||
| chr9:26976913
|
T | C | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-1215T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26976913 | ||||||
| chr9:26977030
|
A | C | 1 | a0001c0001t0001g0128 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.121-1098A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977030 | ||||||
| chr9:26977169
|
G | A | 88 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(85): Show | 88 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.121-959G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977169 | ||||||
| chr9:26977313
|
T | A | 109 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(106): Show | 109 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.121-815T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977313 | ||||||
| chr9:26977331
|
T | C | 109 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(106): Show | 109 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.121-797T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977331 | ||||||
| chr9:26977366
|
G | A | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.121-762G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977366 | ||||||
| chr9:26977562
|
C | A | 32 | a0001c0001t0001g0287a0001c0001t0001g0290a0001c0001t0001g0304others(29): Show | 32 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.121-566C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977562 | ||||||
| chr9:26977567
|
C | T | 1 | a0004c0005t0005g0310 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.121-561C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977567 | ||||||
| chr9:26977689
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.121-439A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977689 | ||||||
| chr9:26977712
|
C | T | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-416C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977712 | ||||||
| chr9:26977769
|
G | A | 89 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(86): Show | 89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.121-359G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977769 | ||||||
| chr9:26977788
|
T | G | 16 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(13): Show | 16 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.121-340T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977788 | ||||||
| chr9:26977804
|
A | G | 30 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(27): Show | 30 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.121-324A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977804 | ||||||
| chr9:26977813
|
A | C | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | NA18612.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.121-315A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977813 | ||||||
| chr9:26977954
|
A | G | 1 | a0006c0006t0001g0335 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.121-174A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26977954 | ||||||
| chr9:26978004
|
A | G | 2 | a0002c0002t0002g0073a0002c0002t0002g0074 | 2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.121-124A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26978004 | ||||||
| chr9:26978050
|
T | C | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-78T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 2/19 | chr9 | 26978050 | ||||||
| chr9:26978305
|
T | G | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.256+42T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26978305 | ||||||
| chr9:26978389
|
T | A | 4 | a0001c0001t0010g0033a0001c0001t0010g0034a0001c0001t0011g0032others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.256+126T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26978389 | ||||||
| chr9:26978462
|
G | A | 1 | a0004c0005t0005g0310 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.256+199G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26978462 | ||||||
| chr9:26978552
|
T | C | 89 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(86): Show | 89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.256+289T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26978552 | ||||||
| chr9:26978627
|
A | C | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0198 | 3 | HG02135.hp1 NA19007.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.256+364A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26978627 | ||||||
| chr9:26978710
|
A | G | 7 | a0006c0006t0001g0328a0006c0006t0001g0329a0006c0006t0001g0330others(4): Show | 7 | HG01257.hp1 HG01515.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.256+447A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26978710 | ||||||
| chr9:26978753
|
T | C | 4 | a0002c0002t0002g0029a0002c0002t0002g0044a0002c0002t0002g0045others(1): Show | 4 | HG00597.hp1 HG02040.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.256+490T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26978753 | ||||||
| chr9:26978953
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.256+690A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26978953 | ||||||
| chr9:26978964
|
C | G | 1 | a0001c0001t0001g0189 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.256+701C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26978964 | ||||||
| chr9:26978988
|
G | A | 20 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(17): Show | 20 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.256+725G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26978988 | ||||||
| chr9:26979029
|
C | T | 109 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(106): Show | 109 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.256+766C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979029 | ||||||
| chr9:26979063
|
A | C | 2 | a0002c0002t0002g0073a0002c0002t0002g0074 | 2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.256+800A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979063 | ||||||
| chr9:26979145
|
A | G | 1 | a0003c0003t0002g0100 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.256+882A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979145 | ||||||
| chr9:26979148
|
T | C | 89 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(86): Show | 89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.256+885T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979148 | ||||||
| chr9:26979151
|
ATT | A | 89 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(86): Show | 89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.256+899_256+900del others(2): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 26979151 | |||||
| chr9:26979362
|
G | C | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.256+1099G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979362 | ||||||
| chr9:26979479
|
T | C | 20 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(17): Show | 20 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.257-1092T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979479 | ||||||
| chr9:26979521
|
C | G | 14 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(11): Show | 14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.257-1050C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979521 | ||||||
| chr9:26979580
|
A | G | 1 | a0002c0002t0002g0072 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.257-991A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979580 | ||||||
| chr9:26979703
|
C | CT | 61 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(58): Show | 61 | HG00323.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.257-841dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 26979703 | |||||
| chr9:26979703
|
C | CTT | 84 | a0001c0001t0001g0108a0001c0001t0015g0130a0001c0001t0018g0127others(81): Show | 84 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.257-842_257-841dup others(2): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 26979703 | |||||
| chr9:26979703
|
C | CTTT | 10 | a0001c0001t0015g0131a0002c0002t0002g0011a0002c0002t0002g0068others(7): Show | 10 | HG01255.hp2 HG01346.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.257-843_257-841dup others(3): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 26979703 | |||||
| chr9:26979703
|
CT | C | 11 | a0001c0001t0001g0149a0001c0001t0001g0178a0001c0001t0001g0179others(8): Show | 11 | HG00099.hp1 HG01074.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.257-841delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 26979703 | |||||
| chr9:26979703
|
CTTTTTTT others(5): Show |
C | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.257-852_257-841del others(12): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 26979703 | |||||
| chr9:26979733
|
G | T | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0198 | 3 | HG02135.hp1 NA19007.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.257-838G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979733 | ||||||
| chr9:26979751
|
C | T | 1 | a0002c0002t0002g0036 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.257-820C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979751 | ||||||
| chr9:26979811
|
C | G | 1 | a0001c0001t0003g0281 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.257-760C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979811 | ||||||
| chr9:26979896
|
G | A | 1 | a0002c0002t0002g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.257-675G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26979896 | ||||||
| chr9:26980004
|
C | T | 4 | a0007c0007t0008g0003a0007c0007t0008g0004a0007c0007t0023g0005others(1): Show | 4 | HG02615.hp1 HG03209.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.257-567C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26980004 | ||||||
| chr9:26980005
|
G | A | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.257-566G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26980005 | ||||||
| chr9:26980068
|
T | C | 1 | a0001c0001t0018g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.257-503T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26980068 | ||||||
| chr9:26980182
|
A | G | 31 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(28): Show | 31 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.257-389A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26980182 | ||||||
| chr9:26980187
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.257-384T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26980187 | ||||||
| chr9:26980281
|
C | G | 13 | a0006c0006t0001g0325a0006c0006t0001g0326a0006c0006t0001g0327others(10): Show | 13 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.257-290C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26980281 | ||||||
| chr9:26980370
|
G | A | 1 | a0007c0007t0006g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.257-201G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26980370 | ||||||
| chr9:26980415
|
A | G | 20 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(17): Show | 20 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.257-156A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26980415 | ||||||
| chr9:26980457
|
G | A | 1 | a0002c0002t0002g0047 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.257-114G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26980457 | ||||||
| chr9:26980568
|
T | C | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.257-3T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 3/19 | chr9 | 26980568 | ||||||
| chr9:26980645
|
G | A | 1 | a0011c0010t0017g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.305+26G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26980645 | ||||||
| chr9:26980802
|
G | T | 1 | a0012c0014t0003g0282 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.305+183G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26980802 | ||||||
| chr9:26980839
|
A | T | 1 | a0006c0006t0001g0332 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.305+220A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26980839 | ||||||
| chr9:26980881
|
C | T | 37 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0135others(34): Show | 37 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.305+262C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26980881 | ||||||
| chr9:26980951
|
C | T | 20 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(17): Show | 20 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.305+332C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26980951 | ||||||
| chr9:26980958
|
C | T | 4 | a0001c0001t0010g0033a0001c0001t0010g0034a0001c0001t0011g0032others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.305+339C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26980958 | ||||||
| chr9:26981029
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.305+410G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26981029 | ||||||
| chr9:26981117
|
C | T | 20 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(17): Show | 20 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.305+498C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26981117 | ||||||
| chr9:26981377
|
G | A | 13 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(10): Show | 13 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.305+758G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26981377 | ||||||
| chr9:26981566
|
C | T | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.305+947C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26981566 | ||||||
| chr9:26981600
|
A | G | 13 | a0006c0006t0001g0325a0006c0006t0001g0326a0006c0006t0001g0327others(10): Show | 13 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.305+981A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26981600 | ||||||
| chr9:26981768
|
A | AT | 13 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0165others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.305+1166dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 26981768 | |||||
| chr9:26981768
|
AT | A | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0198others(5): Show | 8 | HG01070.hp2 HG01358.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.305+1166delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 26981768 | |||||
| chr9:26981814
|
C | T | 12 | a0006c0006t0001g0325a0006c0006t0001g0326a0006c0006t0001g0327others(9): Show | 12 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.305+1195C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26981814 | ||||||
| chr9:26981863
|
G | T | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.305+1244G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26981863 | ||||||
| chr9:26982084
|
GT | G | 16 | a0001c0001t0018g0127a0006c0006t0001g0325a0006c0006t0001g0326others(13): Show | 16 | HG01069.hp2 HG01070.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.305+1473delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 26982084 | |||||
| chr9:26982181
|
T | TA | 4 | a0001c0001t0010g0033a0001c0001t0010g0034a0001c0001t0011g0032others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.305+1562_305+1563i others(3): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26982181 | ||||||
| chr9:26982182
|
G | C | 4 | a0001c0001t0010g0033a0001c0001t0010g0034a0001c0001t0011g0032others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.305+1563G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26982182 | ||||||
| chr9:26982272
|
CT | C | 308 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(305): Show | 308 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.305+1663delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 26982272 | |||||
| chr9:26982287
|
C | T | 1 | a0002c0002t0002g0075 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.305+1668C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26982287 | ||||||
| chr9:26982288
|
G | A | 1 | a0005c0004t0004g0019 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.305+1669G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26982288 | ||||||
| chr9:26982451
|
A | AT | 56 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0135others(53): Show | 56 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.306-1784dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 26982451 | |||||
| chr9:26982451
|
A | ATT | 10 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0199others(7): Show | 10 | HG01123.hp1 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.306-1785_306-1784d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 26982451 | |||||
| chr9:26982451
|
AT | A | 23 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(20): Show | 23 | HG00323.hp2 HG01167.hp1 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.306-1784delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 26982451 | |||||
| chr9:26982451
|
ATTTTTTT | A | 6 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(3): Show | 6 | NA18944.hp2 NA18966.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.306-1790_306-1784d others(9): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 26982451 | |||||
| chr9:26982541
|
C | T | 1 | a0003c0003t0002g0067 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.306-1716C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26982541 | ||||||
| chr9:26982871
|
C | T | 13 | a0006c0006t0001g0325a0006c0006t0001g0326a0006c0006t0001g0327others(10): Show | 13 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.306-1386C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26982871 | ||||||
| chr9:26982881
|
C | T | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.306-1376C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26982881 | ||||||
| chr9:26982968
|
C | T | 1 | a0002c0002t0002g0066 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.306-1289C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26982968 | ||||||
| chr9:26982975
|
G | T | 1 | a0006c0006t0001g0332 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.306-1282G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26982975 | ||||||
| chr9:26983275
|
G | A | 12 | a0006c0006t0001g0325a0006c0006t0001g0326a0006c0006t0001g0327others(9): Show | 12 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.306-982G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26983275 | ||||||
| chr9:26983303
|
T | C | 1 | a0001c0001t0001g0244 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.306-954T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26983303 | ||||||
| chr9:26983440
|
A | G | 31 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(28): Show | 31 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.306-817A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26983440 | ||||||
| chr9:26983562
|
C | T | 1 | a0001c0001t0001g0307 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.306-695C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26983562 | ||||||
| chr9:26983573
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.306-684A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26983573 | ||||||
| chr9:26983610
|
A | G | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | HG00423.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.306-647A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26983610 | ||||||
| chr9:26983776
|
C | CT | 12 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0254others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.306-458dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 26983776 | |||||
| chr9:26983776
|
CT | C | 13 | a0001c0001t0001g0138a0001c0001t0001g0153a0001c0001t0001g0210others(10): Show | 13 | HG00099.hp2 HG00558.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.306-458delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 26983776 | |||||
| chr9:26983799
|
T | C | 1 | a0007c0007t0006g0025 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.306-458T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26983799 | ||||||
| chr9:26983841
|
T | G | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.306-416T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26983841 | ||||||
| chr9:26983975
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.306-282G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26983975 | ||||||
| chr9:26984024
|
T | G | 1 | a0001c0001t0003g0294 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.306-233T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26984024 | ||||||
| chr9:26984029
|
C | A | 1 | a0002c0002t0002g0050 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.306-228C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26984029 | ||||||
| chr9:26984172
|
C | T | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.306-85C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 4/19 | chr9 | 26984172 | ||||||
| chr9:26984426
|
T | A | 5 | a0007c0007t0008g0003a0007c0007t0008g0004a0007c0007t0019g0118others(2): Show | 5 | HG01255.hp2 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.404+71T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 5/19 | chr9 | 26984426 | ||||||
| chr9:26984496
|
C | T | 5 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(2): Show | 5 | HG02056.hp2 NA18960.hp2 NA18973.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.405-3C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 5/19 | chr9 | 26984496 | ||||||
| chr9:26984693
|
A | C | 5 | a0001c0001t0007g0134a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+134A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26984693 | ||||||
| chr9:26984745
|
A | G | 4 | a0001c0001t0001g0153a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 4 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+186A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26984745 | ||||||
| chr9:26985063
|
C | G | 1 | a0001c0001t0001g0307 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.465+504C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26985063 | ||||||
| chr9:26985341
|
G | A | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.465+782G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26985341 | ||||||
| chr9:26985486
|
A | T | 8 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0267others(5): Show | 8 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.465+927A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26985486 | ||||||
| chr9:26985588
|
T | C | 2 | a0003c0003t0002g0110a0003c0003t0002g0111 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.465+1029T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26985588 | ||||||
| chr9:26985729
|
T | A | 3 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026 | 3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.465+1170T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26985729 | ||||||
| chr9:26985795
|
AAC | A | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.465+1240_465+1241d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 26985795 | |||||
| chr9:26985799
|
C | T | 1 | a0001c0001t0025g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.465+1240C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26985799 | ||||||
| chr9:26985852
|
A | G | 2 | a0003c0003t0021g0099a0003c0003t0027g0098 | 2 | NA19077.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.465+1293A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26985852 | ||||||
| chr9:26985927
|
T | C | 13 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(10): Show | 13 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.465+1368T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26985927 | ||||||
| chr9:26986046
|
T | C | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.465+1487T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986046 | ||||||
| chr9:26986152
|
GAAAT | G | 36 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0135others(33): Show | 36 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.465+1597_465+1600d others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 26986152 | |||||
| chr9:26986320
|
G | T | 3 | a0001c0008t0001g0167a0001c0008t0001g0168a0001c0008t0001g0169 | 3 | HG01192.hp2 HG01358.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.465+1761G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986320 | ||||||
| chr9:26986380
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.465+1821A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986380 | ||||||
| chr9:26986510
|
T | C | 93 | a0001c0001t0001g0203a0001c0001t0001g0245a0001c0001t0001g0261others(90): Show | 93 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.465+1951T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986510 | ||||||
| chr9:26986544
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.465+1985T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986544 | ||||||
| chr9:26986561
|
C | A | 1 | a0001c0001t0033g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.465+2002C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986561 | ||||||
| chr9:26986649
|
G | A | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.466-2020G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986649 | ||||||
| chr9:26986776
|
G | C | 24 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(21): Show | 24 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.466-1893G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986776 | ||||||
| chr9:26986839
|
T | G | 2 | a0001c0001t0015g0130a0001c0001t0015g0131 | 2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.466-1830T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986839 | ||||||
| chr9:26986856
|
C | G | 1 | a0011c0010t0017g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.466-1813C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986856 | ||||||
| chr9:26986885
|
A | G | 13 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(10): Show | 13 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.466-1784A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986885 | ||||||
| chr9:26986954
|
C | G | 2 | a0001c0001t0015g0130a0001c0001t0015g0131 | 2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.466-1715C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986954 | ||||||
| chr9:26986974
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.466-1695G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986974 | ||||||
| chr9:26986979
|
G | A | 4 | a0001c0001t0001g0203a0001c0001t0001g0245a0001c0001t0001g0261others(1): Show | 4 | HG00609.hp2 NA18975.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-1690G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26986979 | ||||||
| chr9:26987029
|
G | A | 167 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(164): Show | 167 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.466-1640G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987029 | ||||||
| chr9:26987081
|
G | T | 93 | a0001c0001t0001g0203a0001c0001t0001g0245a0001c0001t0001g0261others(90): Show | 93 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.466-1588G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987081 | ||||||
| chr9:26987132
|
C | A | 3 | a0001c0001t0018g0127a0007c0007t0019g0118a0011c0010t0017g0114 | 3 | HG01255.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.466-1537C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987132 | ||||||
| chr9:26987209
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.466-1460G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987209 | ||||||
| chr9:26987260
|
A | T | 113 | a0001c0001t0001g0203a0001c0001t0001g0245a0001c0001t0001g0261others(110): Show | 113 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.466-1409A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987260 | ||||||
| chr9:26987312
|
A | G | 113 | a0001c0001t0001g0203a0001c0001t0001g0245a0001c0001t0001g0261others(110): Show | 113 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.466-1357A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987312 | ||||||
| chr9:26987382
|
G | A | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.466-1287G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987382 | ||||||
| chr9:26987385
|
C | A | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.466-1284C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987385 | ||||||
| chr9:26987454
|
A | G | 2 | a0003c0003t0002g0110a0003c0003t0002g0111 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.466-1215A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987454 | ||||||
| chr9:26987471
|
A | G | 1 | a0001c0001t0010g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.466-1198A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987471 | ||||||
| chr9:26987495
|
T | G | 31 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(28): Show | 31 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.466-1174T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987495 | ||||||
| chr9:26987688
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.466-981C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987688 | ||||||
| chr9:26987772
|
G | A | 3 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026 | 3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.466-897G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26987772 | ||||||
| chr9:26987877
|
AT | A | 17 | a0001c0001t0001g0152a0001c0001t0001g0176a0001c0001t0001g0179others(14): Show | 17 | HG00597.hp2 HG02129.hp2 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.466-783delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 26987877 | |||||
| chr9:26988055
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0034g0140 | 3 | HG01099.hp2 HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.466-614C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26988055 | ||||||
| chr9:26988087
|
G | A | 4 | a0001c0001t0001g0153a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 4 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-582G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26988087 | ||||||
| chr9:26988247
|
C | T | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.466-422C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26988247 | ||||||
| chr9:26988324
|
T | C | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | HG00423.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.466-345T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26988324 | ||||||
| chr9:26988568
|
T | G | 2 | a0001c0001t0011g0032a0001c0001t0011g0035 | 2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.466-101T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26988568 | ||||||
| chr9:26988573
|
A | G | 115 | a0001c0001t0001g0203a0001c0001t0001g0245a0001c0001t0001g0261others(112): Show | 115 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.466-96A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26988573 | ||||||
| chr9:26988618
|
T | A | 6 | a0001c0001t0010g0033a0001c0001t0010g0034a0007c0007t0008g0003others(3): Show | 6 | HG01884.hp1 HG02615.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-51T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 6/19 | chr9 | 26988618 | ||||||
| chr9:26988785
|
G | A | 14 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(11): Show | 14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.525+57G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26988785 | ||||||
| chr9:26988785
|
G | T | 3 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026 | 3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.525+57G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26988785 | ||||||
| chr9:26988860
|
C | T | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.525+132C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26988860 | ||||||
| chr9:26989187
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.525+459G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26989187 | ||||||
| chr9:26989242
|
A | G | 3 | a0001c0001t0001g0152a0001c0001t0001g0179a0001c0001t0001g0185 | 3 | NA18964.hp2 NA18967.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.525+514A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26989242 | ||||||
| chr9:26989385
|
G | A | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+657G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26989385 | ||||||
| chr9:26989511
|
G | A | 1 | a0002c0002t0002g0050 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.526-623G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26989511 | ||||||
| chr9:26989754
|
A | C | 1 | a0001c0001t0018g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.526-380A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26989754 | ||||||
| chr9:26989766
|
A | C | 1 | a0002c0002t0002g0012 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.526-368A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26989766 | ||||||
| chr9:26989817
|
CA | C | 31 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(28): Show | 31 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.526-314delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr9 | 26989817 | |||||
| chr9:26989954
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.526-180T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26989954 | ||||||
| chr9:26989984
|
G | A | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-150G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26989984 | ||||||
| chr9:26990048
|
A | G | 3 | a0006c0006t0001g0326a0006c0006t0001g0327a0006c0006t0026g0206 | 3 | HG02055.hp2 HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.526-86A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26990048 | ||||||
| chr9:26990083
|
A | T | 1 | a0011c0010t0017g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.526-51A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 7/19 | chr9 | 26990083 | ||||||
| chr9:26990364
|
T | G | 16 | a0002c0002t0002g0051a0002c0002t0002g0076a0002c0002t0002g0077others(13): Show | 16 | HG00558.hp2 HG00609.hp1 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.587+169T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26990364 | ||||||
| chr9:26990388
|
AT | A | 4 | a0001c0001t0001g0149a0001c0001t0001g0186a0001c0001t0001g0195others(1): Show | 4 | HG01074.hp1 HG01175.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.587+194delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26990388 | ||||||
| chr9:26990394
|
A | G | 4 | a0001c0001t0001g0149a0001c0001t0001g0186a0001c0001t0001g0195others(1): Show | 4 | HG01074.hp1 HG01175.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.587+199A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26990394 | ||||||
| chr9:26990444
|
A | G | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.587+249A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26990444 | ||||||
| chr9:26990486
|
G | T | 1 | a0003c0003t0002g0049 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.587+291G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26990486 | ||||||
| chr9:26990661
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.587+466A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26990661 | ||||||
| chr9:26990686
|
G | A | 3 | a0005c0004t0004g0019a0005c0004t0004g0020a0005c0004t0036g0028 | 3 | HG00323.hp2 HG01361.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.587+491G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26990686 | ||||||
| chr9:26990828
|
A | T | 12 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(9): Show | 12 | HG00639.hp2 HG01256.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.587+633A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26990828 | ||||||
| chr9:26990914
|
T | G | 1 | a0005c0004t0004g0019 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.587+719T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26990914 | ||||||
| chr9:26990970
|
A | C | 1 | a0001c0001t0001g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587+775A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26990970 | ||||||
| chr9:26991207
|
T | C | 3 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121 | 3 | HG03041.hp1 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.587+1012T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991207 | ||||||
| chr9:26991329
|
T | C | 5 | a0001c0001t0007g0134a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+1134T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991329 | ||||||
| chr9:26991379
|
C | T | 4 | a0001c0001t0001g0153a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 4 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(1): Show |
intron_variant | MODIFIER | c.587+1184C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991379 | ||||||
| chr9:26991409
|
A | G | 163 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(160): Show | 163 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.587+1214A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991409 | ||||||
| chr9:26991430
|
G | A | 1 | a0002c0002t0002g0052 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.587+1235G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991430 | ||||||
| chr9:26991475
|
C | T | 1 | a0002c0002t0002g0065 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.587+1280C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991475 | ||||||
| chr9:26991516
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.587+1321G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991516 | ||||||
| chr9:26991796
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587+1601C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991796 | ||||||
| chr9:26991801
|
C | T | 2 | a0001c0001t0001g0116a0003c0003t0002g0126 | 2 | HG00408.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.587+1606C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991801 | ||||||
| chr9:26991832
|
C | G | 1 | a0001c0001t0018g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.587+1637C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991832 | ||||||
| chr9:26991832
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.587+1637C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991832 | ||||||
| chr9:26991854
|
C | G | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.587+1659C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991854 | ||||||
| chr9:26991914
|
A | G | 89 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(86): Show | 89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.587+1719A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991914 | ||||||
| chr9:26991946
|
T | C | 3 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026 | 3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.587+1751T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991946 | ||||||
| chr9:26991984
|
G | A | 1 | a0011c0010t0017g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.587+1789G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26991984 | ||||||
| chr9:26992035
|
C | CA | 86 | a0001c0001t0001g0180a0001c0001t0018g0127a0002c0002t0002g0006others(83): Show | 86 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.587+1852dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26992035 | |||||
| chr9:26992047
|
A | C | 1 | a0001c0001t0001g0196 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.587+1852A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992047 | ||||||
| chr9:26992140
|
A | G | 2 | a0001c0001t0010g0033a0001c0001t0010g0034 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.587+1945A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992140 | ||||||
| chr9:26992508
|
T | C | 165 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(162): Show | 166 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.587+2313T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992508 | ||||||
| chr9:26992598
|
C | T | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.587+2403C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992598 | ||||||
| chr9:26992635
|
G | T | 1 | a0006c0006t0001g0327 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.587+2440G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992635 | ||||||
| chr9:26992649
|
C | T | 1 | a0002c0002t0002g0095 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.587+2454C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992649 | ||||||
| chr9:26992658
|
A | G | 14 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(11): Show | 14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.587+2463A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992658 | ||||||
| chr9:26992679
|
C | T | 12 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(9): Show | 12 | HG00639.hp2 HG01256.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.587+2484C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992679 | ||||||
| chr9:26992687
|
T | C | 8 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(5): Show | 8 | HG01891.hp2 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.587+2492T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992687 | ||||||
| chr9:26992692
|
C | CA | 12 | a0001c0001t0001g0103a0001c0001t0001g0263a0001c0001t0001g0264others(9): Show | 12 | HG00408.hp2 HG00558.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.587+2510dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26992692 | |||||
| chr9:26992788
|
G | A | 1 | a0002c0002t0024g0320 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.587+2593G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992788 | ||||||
| chr9:26992860
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0261 | 2 | NA18975.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.587+2665G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26992860 | ||||||
| chr9:26993030
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.587+2835A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26993030 | ||||||
| chr9:26993483
|
G | A | 1 | a0002c0002t0002g0036 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.587+3288G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26993483 | ||||||
| chr9:26993595
|
A | G | 104 | a0001c0001t0018g0127a0002c0002t0002g0006a0002c0002t0002g0007others(101): Show | 104 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.587+3400A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26993595 | ||||||
| chr9:26993642
|
A | G | 2 | a0001c0001t0003g0299a0001c0001t0003g0300 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.587+3447A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26993642 | ||||||
| chr9:26993757
|
T | G | 81 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(78): Show | 81 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.587+3562T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26993757 | ||||||
| chr9:26993796
|
A | G | 13 | a0006c0006t0001g0325a0006c0006t0001g0326a0006c0006t0001g0327others(10): Show | 13 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.587+3601A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26993796 | ||||||
| chr9:26993891
|
T | C | 88 | a0001c0001t0018g0127a0002c0002t0002g0006a0002c0002t0002g0007others(85): Show | 88 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.587+3696T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26993891 | ||||||
| chr9:26994223
|
A | T | 81 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(78): Show | 81 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.587+4028A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994223 | ||||||
| chr9:26994331
|
G | A | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.587+4136G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994331 | ||||||
| chr9:26994331
|
G | C | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.587+4136G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994331 | ||||||
| chr9:26994382
|
C | T | 1 | a0011c0010t0017g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.587+4187C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994382 | ||||||
| chr9:26994469
|
G | A | 1 | a0003c0003t0002g0037 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.587+4274G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994469 | ||||||
| chr9:26994493
|
C | T | 2 | a0001c0001t0001g0203a0001c0001t0001g0307 | 2 | HG00609.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.587+4298C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994493 | ||||||
| chr9:26994536
|
C | CA | 18 | a0001c0001t0001g0107a0001c0001t0001g0132a0001c0001t0001g0165others(15): Show | 18 | HG01123.hp2 HG01255.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.587+4361dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26994536 | |||||
| chr9:26994536
|
CA | C | 8 | a0001c0001t0001g0153a0001c0001t0001g0159a0001c0001t0001g0208others(5): Show | 8 | HG00099.hp2 HG03209.hp2 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.587+4361delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26994536 | |||||
| chr9:26994600
|
C | A | 5 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 5 | HG01891.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+4405C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994600 | ||||||
| chr9:26994800
|
G | A | 332 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(329): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.587+4605G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994800 | ||||||
| chr9:26994856
|
G | A | 1 | a0007c0007t0019g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.587+4661G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994856 | ||||||
| chr9:26994868
|
T | G | 2 | a0001c0001t0011g0032a0001c0001t0011g0035 | 2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.587+4673T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994868 | ||||||
| chr9:26994932
|
T | C | 1 | a0001c0001t0001g0191 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.587+4737T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994932 | ||||||
| chr9:26994971
|
A | C | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.587+4776A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26994971 | ||||||
| chr9:26995155
|
A | G | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.587+4960A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26995155 | ||||||
| chr9:26995249
|
T | G | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+5054T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26995249 | ||||||
| chr9:26995789
|
G | A | 16 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(13): Show | 16 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.587+5594G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26995789 | ||||||
| chr9:26995888
|
T | C | 17 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(14): Show | 17 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.587+5693T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26995888 | ||||||
| chr9:26995903
|
A | G | 1 | a0001c0008t0001g0169 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.587+5708A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26995903 | ||||||
| chr9:26995929
|
C | T | 17 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(14): Show | 17 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.587+5734C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26995929 | ||||||
| chr9:26996172
|
G | C | 150 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(147): Show | 150 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.587+5977G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26996172 | ||||||
| chr9:26996432
|
A | C | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.587+6237A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26996432 | ||||||
| chr9:26996478
|
C | T | 1 | a0002c0002t0002g0086 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.587+6283C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26996478 | ||||||
| chr9:26996608
|
T | A | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.587+6413T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26996608 | ||||||
| chr9:26996627
|
T | C | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.587+6432T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26996627 | ||||||
| chr9:26996720
|
A | G | 1 | a0001c0001t0014g0001 | 2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.587+6525A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26996720 | ||||||
| chr9:26996721
|
T | C | 2 | a0003c0003t0002g0110a0003c0003t0002g0111 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.587+6526T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26996721 | ||||||
| chr9:26996770
|
A | T | 87 | a0001c0001t0018g0127a0002c0002t0002g0006a0002c0002t0002g0007others(84): Show | 87 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.587+6575A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26996770 | ||||||
| chr9:26996939
|
A | G | 8 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(5): Show | 8 | HG01891.hp2 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.587+6744A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26996939 | ||||||
| chr9:26996980
|
G | T | 13 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(10): Show | 13 | HG01192.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.587+6785G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26996980 | ||||||
| chr9:26997056
|
C | G | 87 | a0001c0001t0018g0127a0002c0002t0002g0006a0002c0002t0002g0007others(84): Show | 87 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.587+6861C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997056 | ||||||
| chr9:26997168
|
C | T | 2 | a0001c0001t0003g0299a0001c0001t0003g0300 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.587+6973C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997168 | ||||||
| chr9:26997209
|
T | C | 1 | a0004c0005t0005g0319 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.587+7014T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997209 | ||||||
| chr9:26997212
|
CA | C | 125 | a0001c0001t0001g0188a0001c0001t0018g0127a0002c0002t0002g0006others(122): Show | 125 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.587+7031delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26997212 | |||||
| chr9:26997234
|
A | AT | 9 | a0002c0002t0002g0010a0003c0003t0002g0038a0003c0003t0002g0088others(6): Show | 9 | HG00408.hp1 HG02523.hp2 NA18973.hp2 others(6): Show |
intron_variant | MODIFIER | c.587+7044dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26997234 | |||||
| chr9:26997256
|
A | G | 1 | a0004c0005t0005g0312 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.587+7061A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997256 | ||||||
| chr9:26997257
|
AGGAGAGC others(3): Show |
A | 1 | a0004c0005t0005g0312 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.587+7063_587+7072d others(12): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997257 | ||||||
| chr9:26997268
|
T | A | 1 | a0004c0005t0005g0312 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.587+7073T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997268 | ||||||
| chr9:26997330
|
C | CT | 84 | a0001c0001t0001g0176a0001c0001t0001g0180a0001c0001t0001g0193others(81): Show | 84 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.587+7156dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26997330 | |||||
| chr9:26997330
|
C | CTT | 6 | a0002c0002t0002g0006a0002c0002t0002g0064a0002c0002t0002g0068others(3): Show | 6 | NA18959.hp1 NA18967.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.587+7155_587+7156d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26997330 | |||||
| chr9:26997330
|
CTTTT | C | 7 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(4): Show | 7 | HG01891.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.587+7153_587+7156d others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26997330 | |||||
| chr9:26997375
|
C | T | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.587+7180C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997375 | ||||||
| chr9:26997396
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.587+7201C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997396 | ||||||
| chr9:26997414
|
A | G | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.587+7219A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997414 | ||||||
| chr9:26997415
|
C | T | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.587+7220C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997415 | ||||||
| chr9:26997444
|
C | G | 1 | a0007c0007t0008g0004 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.587+7249C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997444 | ||||||
| chr9:26997445
|
C | G | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.587+7250C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997445 | ||||||
| chr9:26997458
|
T | C | 8 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(5): Show | 8 | HG01891.hp2 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.587+7263T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997458 | ||||||
| chr9:26997554
|
A | T | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.587+7359A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997554 | ||||||
| chr9:26997558
|
T | A | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.587+7363T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997558 | ||||||
| chr9:26997606
|
T | G | 1 | a0001c0001t0001g0287 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.587+7411T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997606 | ||||||
| chr9:26997626
|
G | A | 1 | a0001c0001t0018g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.587+7431G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997626 | ||||||
| chr9:26997982
|
T | C | 1 | a0001c0008t0001g0168 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.587+7787T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26997982 | ||||||
| chr9:26998049
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.587+7854C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998049 | ||||||
| chr9:26998092
|
C | T | 5 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0251others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.587+7897C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998092 | ||||||
| chr9:26998191
|
A | T | 3 | a0001c0001t0001g0287a0001c0001t0001g0290a0001c0001t0001g0304 | 3 | HG02257.hp2 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.587+7996A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998191 | ||||||
| chr9:26998251
|
C | T | 8 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(5): Show | 8 | HG01891.hp2 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.587+8056C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998251 | ||||||
| chr9:26998325
|
A | C | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.587+8130A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998325 | ||||||
| chr9:26998335
|
C | T | 14 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0135others(11): Show | 14 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.587+8140C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998335 | ||||||
| chr9:26998347
|
A | G | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.587+8152A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998347 | ||||||
| chr9:26998535
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.587+8340C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998535 | ||||||
| chr9:26998555
|
G | A | 306 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(303): Show | 306 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.587+8360G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998555 | ||||||
| chr9:26998777
|
A | T | 12 | a0006c0006t0001g0325a0006c0006t0001g0326a0006c0006t0001g0327others(9): Show | 12 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.587+8582A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998777 | ||||||
| chr9:26998817
|
C | T | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.587+8622C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998817 | ||||||
| chr9:26998829
|
C | CA | 6 | a0001c0001t0001g0163a0001c0001t0015g0131a0002c0002t0002g0076others(3): Show | 6 | HG00558.hp2 HG02738.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.587+8648dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26998829 | |||||
| chr9:26998829
|
CAA | C | 8 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(5): Show | 8 | HG01891.hp2 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.587+8647_587+8648d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26998829 | |||||
| chr9:26998835
|
A | T | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.587+8640A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998835 | ||||||
| chr9:26998850
|
C | A | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.587+8655C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998850 | ||||||
| chr9:26998851
|
G | A | 31 | a0001c0001t0001g0287a0001c0001t0001g0290a0001c0001t0001g0304others(28): Show | 31 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.587+8656G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998851 | ||||||
| chr9:26998851
|
G | C | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.587+8656G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26998851 | ||||||
| chr9:26999011
|
C | T | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.587+8816C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26999011 | ||||||
| chr9:26999013
|
A | T | 28 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(25): Show | 28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.587+8818A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26999013 | ||||||
| chr9:26999116
|
G | A | 14 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(11): Show | 14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.587+8921G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26999116 | ||||||
| chr9:26999168
|
A | ATATAATT others(11): Show |
1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.587+8977_587+8978i others(20): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26999168 | |||||
| chr9:26999185
|
G | T | 1 | a0001c0001t0001g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.587+8990G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26999185 | ||||||
| chr9:26999770
|
C | CT | 152 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0106others(149): Show | 152 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.588-9229dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26999770 | |||||
| chr9:26999770
|
C | CTT | 16 | a0001c0001t0001g0237a0001c0001t0001g0251a0001c0001t0001g0252others(13): Show | 16 | HG01167.hp2 HG01169.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.588-9230_588-9229d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26999770 | |||||
| chr9:26999770
|
CT | C | 17 | a0001c0001t0001g0181a0001c0001t0001g0241a0001c0001t0001g0263others(14): Show | 17 | HG00408.hp2 HG00558.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.588-9229delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 26999770 | |||||
| chr9:26999833
|
A | G | 5 | a0001c0001t0007g0134a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.588-9187A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26999833 | ||||||
| chr9:26999842
|
G | A | 99 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0203others(96): Show | 99 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.588-9178G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26999842 | ||||||
| chr9:26999920
|
A | C | 1 | a0002c0002t0002g0063 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.588-9100A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 26999920 | ||||||
| chr9:27000238
|
G | A | 3 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026 | 3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.588-8782G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27000238 | ||||||
| chr9:27000342
|
C | T | 163 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(160): Show | 163 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.588-8678C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27000342 | ||||||
| chr9:27000500
|
A | G | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.588-8520A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27000500 | ||||||
| chr9:27000746
|
G | A | 2 | a0003c0003t0002g0042a0003c0003t0002g0049 | 2 | HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.588-8274G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27000746 | ||||||
| chr9:27000766
|
C | T | 1 | a0001c0001t0003g0298 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.588-8254C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27000766 | ||||||
| chr9:27000849
|
A | G | 14 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(11): Show | 14 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.588-8171A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27000849 | ||||||
| chr9:27001109
|
G | A | 1 | a0010c0013t0031g0284 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.588-7911G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27001109 | ||||||
| chr9:27001135
|
T | G | 1 | a0011c0010t0017g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.588-7885T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27001135 | ||||||
| chr9:27001191
|
T | A | 28 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(25): Show | 28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.588-7829T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27001191 | ||||||
| chr9:27001215
|
A | C | 4 | a0007c0007t0008g0003a0007c0007t0008g0004a0007c0007t0023g0005others(1): Show | 4 | HG02615.hp1 HG03209.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.588-7805A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27001215 | ||||||
| chr9:27001238
|
G | A | 1 | a0001c0012t0003g0302 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.588-7782G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27001238 | ||||||
| chr9:27001380
|
CT | C | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.588-7638delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27001380 | |||||
| chr9:27001588
|
G | GT | 17 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(14): Show | 17 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.588-7429dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27001588 | |||||
| chr9:27001601
|
G | T | 1 | a0002c0002t0002g0084 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.588-7419G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27001601 | ||||||
| chr9:27001602
|
T | A | 1 | a0002c0002t0002g0084 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.588-7418T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27001602 | ||||||
| chr9:27001603
|
G | A | 1 | a0002c0002t0002g0084 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.588-7417G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27001603 | ||||||
| chr9:27001647
|
G | A | 2 | a0001c0001t0003g0299a0001c0001t0003g0300 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.588-7373G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27001647 | ||||||
| chr9:27001942
|
C | CT | 42 | a0001c0001t0001g0240a0001c0001t0001g0287a0001c0001t0001g0290others(39): Show | 42 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.588-7066dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27001942 | |||||
| chr9:27001942
|
CT | C | 14 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0001g0166others(11): Show | 14 | HG01515.hp2 HG01891.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.588-7066delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27001942 | |||||
| chr9:27002004
|
T | A | 332 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(329): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.588-7016T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002004 | ||||||
| chr9:27002009
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.588-7011G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002009 | ||||||
| chr9:27002013
|
G | T | 4 | a0007c0007t0008g0003a0007c0007t0008g0004a0007c0007t0023g0005others(1): Show | 4 | HG02615.hp1 HG03209.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.588-7007G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002013 | ||||||
| chr9:27002026
|
G | A | 1 | a0012c0014t0003g0282 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.588-6994G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002026 | ||||||
| chr9:27002196
|
A | C | 1 | a0001c0001t0001g0178 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.588-6824A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002196 | ||||||
| chr9:27002319
|
C | G | 1 | a0001c0001t0033g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.588-6701C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002319 | ||||||
| chr9:27002367
|
G | T | 1 | a0001c0001t0001g0243 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.588-6653G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002367 | ||||||
| chr9:27002378
|
G | A | 1 | a0002c0002t0002g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.588-6642G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002378 | ||||||
| chr9:27002514
|
G | C | 25 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(22): Show | 25 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.588-6506G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002514 | ||||||
| chr9:27002568
|
C | A | 13 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(10): Show | 13 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.588-6452C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002568 | ||||||
| chr9:27002612
|
T | A | 1 | a0001c0001t0001g0210 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.588-6408T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002612 | ||||||
| chr9:27002613
|
A | T | 1 | a0001c0001t0001g0210 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.588-6407A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002613 | ||||||
| chr9:27002782
|
T | C | 17 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(14): Show | 17 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.588-6238T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002782 | ||||||
| chr9:27002828
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.588-6192G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002828 | ||||||
| chr9:27002830
|
G | A | 4 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0198others(1): Show | 4 | HG02135.hp1 HG03209.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.588-6190G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27002830 | ||||||
| chr9:27003205
|
G | GT | 18 | a0002c0002t0002g0084a0005c0004t0004g0013a0005c0004t0004g0014others(15): Show | 18 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.588-5805dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27003205 | |||||
| chr9:27003277
|
C | T | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.588-5743C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27003277 | ||||||
| chr9:27003352
|
A | C | 3 | a0001c0001t0001g0287a0001c0001t0001g0290a0001c0001t0001g0304 | 3 | HG02257.hp2 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.588-5668A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27003352 | ||||||
| chr9:27003388
|
T | A | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.588-5632T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27003388 | ||||||
| chr9:27003514
|
C | G | 3 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026 | 3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.588-5506C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27003514 | ||||||
| chr9:27003554
|
G | T | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.588-5466G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27003554 | ||||||
| chr9:27003557
|
A | G | 1 | a0011c0010t0017g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.588-5463A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27003557 | ||||||
| chr9:27003849
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.588-5171G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27003849 | ||||||
| chr9:27003899
|
T | C | 1 | a0001c0001t0033g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.588-5121T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27003899 | ||||||
| chr9:27003919
|
C | T | 1 | a0011c0010t0017g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.588-5101C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27003919 | ||||||
| chr9:27003994
|
G | A | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.588-5026G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27003994 | ||||||
| chr9:27004198
|
A | C | 3 | a0001c0001t0003g0272a0001c0001t0003g0273a0001c0001t0003g0274 | 3 | HG01069.hp1 HG03654.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.588-4822A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27004198 | ||||||
| chr9:27004312
|
CTTGGAAG others(57): Show |
C | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.588-4707_588-4644d others(66): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27004312 | ||||||
| chr9:27004340
|
G | A | 35 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0135others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.588-4680G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27004340 | ||||||
| chr9:27004379
|
A | G | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.588-4641A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27004379 | ||||||
| chr9:27005022
|
A | T | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.588-3998A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005022 | ||||||
| chr9:27005064
|
A | G | 92 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0250others(89): Show | 92 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.588-3956A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005064 | ||||||
| chr9:27005066
|
G | A | 27 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0115others(24): Show | 27 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.588-3954G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005066 | ||||||
| chr9:27005130
|
A | AT | 4 | a0002c0002t0002g0068a0007c0007t0008g0003a0007c0007t0008g0004others(1): Show | 4 | HG02615.hp1 HG03579.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.588-3883dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005130 | |||||
| chr9:27005229
|
A | T | 1 | a0001c0001t0001g0252 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.588-3791A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005229 | ||||||
| chr9:27005296
|
T | C | 2 | a0001c0001t0013g0265a0001c0001t0013g0266 | 2 | NA18959.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.588-3724T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005296 | ||||||
| chr9:27005351
|
T | TC | 3 | a0001c0001t0001g0152a0001c0001t0001g0209a0001c0001t0032g0224 | 3 | NA18612.hp2 NA18964.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.588-3669_588-3668i others(3): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005351 | ||||||
| chr9:27005352
|
T | C | 9 | a0001c0001t0001g0152a0001c0001t0001g0176a0001c0001t0001g0179others(6): Show | 9 | HG00597.hp2 HG00741.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.588-3668T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005352 | ||||||
| chr9:27005352
|
T | TC | 74 | a0001c0001t0001g0103a0001c0001t0001g0120a0001c0001t0001g0132others(71): Show | 75 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.588-3660dupC | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | |||||
| chr9:27005352
|
T | TCC | 17 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0154others(14): Show | 17 | HG01074.hp2 HG01175.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.588-3661_588-3660d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | |||||
| chr9:27005352
|
T | TCCACCCC others(7): Show |
2 | a0003c0003t0002g0322a0003c0003t0002g0323 | 2 | HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.588-3666_588-3665i others(16): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | |||||
| chr9:27005352
|
T | TCCACCCC others(9): Show |
1 | a0003c0003t0002g0324 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.588-3666_588-3665i others(18): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | |||||
| chr9:27005352
|
T | TCCACCCC others(10): Show |
1 | a0003c0003t0002g0321 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.588-3666_588-3665i others(19): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | |||||
| chr9:27005352
|
T | TCCCCCG | 25 | a0001c0001t0001g0250a0001c0001t0001g0255a0002c0002t0002g0010others(22): Show | 25 | HG00408.hp1 HG00558.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.588-3663_588-3662i others(8): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | |||||
| chr9:27005352
|
T | TCCCCCGC | 23 | a0002c0002t0002g0006a0002c0002t0002g0008a0002c0002t0002g0009others(20): Show | 23 | HG00597.hp1 HG01346.hp2 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.588-3663_588-3662i others(9): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | |||||
| chr9:27005352
|
T | TCCCCCGC others(1): Show |
18 | a0001c0001t0001g0230a0001c0001t0001g0252a0002c0002t0002g0007others(15): Show | 18 | HG00621.hp1 HG00621.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.588-3663_588-3662i others(10): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | |||||
| chr9:27005352
|
T | TCCCCCGC others(3): Show |
2 | a0002c0002t0002g0047a0002c0002t0002g0056 | 2 | HG01255.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.588-3663_588-3662i others(12): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | |||||
| chr9:27005352
|
T | TCCCCCGC others(4): Show |
2 | a0002c0002t0002g0084a0002c0002t0002g0125 | 2 | HG02135.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.588-3663_588-3662i others(13): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | |||||
| chr9:27005352
|
T | TCCCCCGC others(6): Show |
1 | a0002c0002t0002g0070 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.588-3663_588-3662i others(15): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005352 | |||||
| chr9:27005355
|
C | G | 6 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0158others(3): Show | 6 | HG00423.hp1 HG02080.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.588-3665C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005355 | ||||||
| chr9:27005357
|
C | G | 5 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 5 | HG01891.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.588-3663C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005357 | ||||||
| chr9:27005360
|
CG | C | 52 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(49): Show | 52 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.588-3659delG | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005360 | ||||||
| chr9:27005361
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0028g0301 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.588-3659G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005361 | ||||||
| chr9:27005361
|
G | C | 266 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0117others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.588-3659G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005361 | ||||||
| chr9:27005363
|
C | G | 1 | a0001c0001t0003g0283 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.588-3657C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005363 | ||||||
| chr9:27005429
|
T | C | 8 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(5): Show | 8 | HG01891.hp2 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.588-3591T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005429 | ||||||
| chr9:27005454
|
G | C | 3 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026 | 3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.588-3566G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005454 | ||||||
| chr9:27005489
|
T | C | 1 | a0001c0001t0033g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.588-3531T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005489 | ||||||
| chr9:27005545
|
TA | T | 5 | a0001c0001t0010g0033a0001c0001t0010g0034a0007c0007t0006g0016others(2): Show | 5 | HG00733.hp1 HG01884.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.588-3467delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005545 | |||||
| chr9:27005546
|
A | T | 4 | a0007c0007t0008g0003a0007c0007t0008g0004a0007c0007t0023g0005others(1): Show | 4 | HG02615.hp1 HG03209.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.588-3474A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005546 | ||||||
| chr9:27005567
|
A | G | 32 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(29): Show | 32 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.588-3453A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005567 | ||||||
| chr9:27005572
|
T | A | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.588-3448T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005572 | ||||||
| chr9:27005620
|
G | A | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.588-3400G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005620 | ||||||
| chr9:27005659
|
A | G | 1 | a0001c0001t0018g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.588-3361A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005659 | ||||||
| chr9:27005756
|
T | C | 1 | a0001c0001t0018g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.588-3264T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005756 | ||||||
| chr9:27005841
|
C | CT | 30 | a0001c0001t0001g0240a0001c0001t0001g0287a0001c0001t0001g0290others(27): Show | 30 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.588-3171dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27005841 | |||||
| chr9:27005862
|
T | C | 208 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(205): Show | 208 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.588-3158T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005862 | ||||||
| chr9:27005944
|
G | A | 5 | a0001c0001t0007g0134a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.588-3076G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27005944 | ||||||
| chr9:27006127
|
A | T | 1 | a0001c0001t0001g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.588-2893A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27006127 | ||||||
| chr9:27006340
|
G | A | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.588-2680G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27006340 | ||||||
| chr9:27006515
|
G | A | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.588-2505G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27006515 | ||||||
| chr9:27006550
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.588-2470T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27006550 | ||||||
| chr9:27006577
|
A | G | 105 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0203others(102): Show | 105 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.588-2443A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27006577 | ||||||
| chr9:27006623
|
A | AAG | 17 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(14): Show | 17 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.588-2381_588-2380d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27006623 | |||||
| chr9:27006623
|
AAGAG | A | 5 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 5 | HG01891.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.588-2383_588-2380d others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27006623 | |||||
| chr9:27006749
|
A | G | 6 | a0001c0001t0001g0119a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG01496.hp1 HG02615.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.588-2271A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27006749 | ||||||
| chr9:27006761
|
A | C | 3 | a0001c0001t0010g0033a0001c0001t0010g0034a0007c0007t0019g0118 | 3 | HG01255.hp2 HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.588-2259A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27006761 | ||||||
| chr9:27006831
|
G | GT | 28 | a0001c0001t0001g0102a0001c0001t0001g0107a0001c0001t0001g0115others(25): Show | 28 | HG00609.hp2 HG00621.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.588-2166dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27006831 | |||||
| chr9:27006831
|
GT | G | 146 | a0001c0001t0001g0120a0001c0001t0001g0132a0001c0001t0001g0133others(143): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.588-2166delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27006831 | |||||
| chr9:27006831
|
GTT | G | 7 | a0001c0001t0001g0216a0001c0001t0001g0243a0001c0001t0001g0287others(4): Show | 7 | HG00323.hp1 HG01069.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-2167_588-2166d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27006831 | |||||
| chr9:27006859
|
T | C | 1 | a0001c0001t0003g0281 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.588-2161T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27006859 | ||||||
| chr9:27006981
|
C | T | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.588-2039C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27006981 | ||||||
| chr9:27007047
|
A | C | 1 | a0006c0006t0001g0336 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.588-1973A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27007047 | ||||||
| chr9:27007084
|
G | A | 1 | a0006c0006t0001g0325 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.588-1936G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27007084 | ||||||
| chr9:27007129
|
G | T | 1 | a0007c0007t0008g0004 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.588-1891G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27007129 | ||||||
| chr9:27007392
|
G | A | 3 | a0005c0004t0004g0018a0005c0004t0004g0022a0005c0004t0004g0023 | 3 | HG00733.hp2 HG01934.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.588-1628G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27007392 | ||||||
| chr9:27007639
|
A | G | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.588-1381A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27007639 | ||||||
| chr9:27007856
|
G | T | 1 | a0002c0002t0002g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.588-1164G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27007856 | ||||||
| chr9:27007906
|
C | T | 17 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(14): Show | 17 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.588-1114C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27007906 | ||||||
| chr9:27007923
|
G | C | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.588-1097G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27007923 | ||||||
| chr9:27007924
|
T | C | 2 | a0003c0003t0002g0042a0003c0003t0002g0049 | 2 | HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.588-1096T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27007924 | ||||||
| chr9:27008314
|
A | G | 2 | a0003c0003t0002g0322a0003c0003t0002g0323 | 2 | HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.588-706A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27008314 | ||||||
| chr9:27008397
|
G | T | 1 | a0007c0007t0019g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.588-623G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27008397 | ||||||
| chr9:27008409
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.588-611G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27008409 | ||||||
| chr9:27008420
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.588-600C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27008420 | ||||||
| chr9:27008559
|
C | T | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.588-461C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27008559 | ||||||
| chr9:27008645
|
C | T | 9 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(6): Show | 9 | HG01496.hp1 HG01891.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.588-375C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27008645 | ||||||
| chr9:27008654
|
G | A | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.588-366G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27008654 | ||||||
| chr9:27008666
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.588-354T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27008666 | ||||||
| chr9:27008818
|
TA | T | 5 | a0007c0007t0008g0003a0007c0007t0008g0004a0007c0007t0019g0118others(2): Show | 5 | HG01255.hp2 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.588-197delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 27008818 | |||||
| chr9:27008986
|
T | A | 2 | a0001c0001t0010g0033a0001c0001t0010g0034 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.588-34T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 8/19 | chr9 | 27008986 | ||||||
| chr9:27009241
|
C | T | 3 | a0001c0001t0001g0178a0001c0001t0001g0187a0001c0001t0001g0188 | 3 | HG00099.hp1 HG00140.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.726+83C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009241 | ||||||
| chr9:27009293
|
C | G | 1 | a0001c0001t0001g0194 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.726+135C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009293 | ||||||
| chr9:27009297
|
C | A | 1 | a0001c0001t0001g0241 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.726+139C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009297 | ||||||
| chr9:27009307
|
C | T | 81 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(78): Show | 81 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.726+149C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009307 | ||||||
| chr9:27009308
|
G | A | 1 | a0002c0002t0002g0051 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.726+150G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009308 | ||||||
| chr9:27009346
|
C | A | 14 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(11): Show | 14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.726+188C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009346 | ||||||
| chr9:27009405
|
A | G | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.726+247A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009405 | ||||||
| chr9:27009478
|
C | T | 5 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0250others(2): Show | 5 | NA18988.hp2 NA18998.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.726+320C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009478 | ||||||
| chr9:27009492
|
C | T | 2 | a0004c0005t0005g0311a0004c0005t0005g0317 | 2 | HG01256.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.726+334C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009492 | ||||||
| chr9:27009581
|
C | T | 99 | a0001c0001t0018g0127a0002c0002t0002g0006a0002c0002t0002g0007others(96): Show | 99 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.726+423C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009581 | ||||||
| chr9:27009658
|
C | T | 1 | a0007c0007t0019g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.726+500C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009658 | ||||||
| chr9:27009686
|
C | G | 14 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(11): Show | 14 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.726+528C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009686 | ||||||
| chr9:27009740
|
A | C | 14 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(11): Show | 14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.726+582A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009740 | ||||||
| chr9:27009853
|
A | C | 1 | a0005c0004t0004g0275 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.726+695A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009853 | ||||||
| chr9:27009914
|
G | A | 1 | a0001c0001t0018g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.726+756G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009914 | ||||||
| chr9:27009971
|
AT | A | 17 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(14): Show | 17 | HG00639.hp2 HG01256.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.726+826delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr9 | 27009971 | |||||
| chr9:27009984
|
T | A | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.726+826T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27009984 | ||||||
| chr9:27010081
|
G | A | 8 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0246others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.726+923G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010081 | ||||||
| chr9:27010181
|
G | C | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.726+1023G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010181 | ||||||
| chr9:27010193
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.726+1035G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010193 | ||||||
| chr9:27010208
|
C | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | NA18612.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.726+1050C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010208 | ||||||
| chr9:27010225
|
G | A | 8 | a0003c0003t0002g0038a0003c0003t0002g0088a0003c0003t0002g0089others(5): Show | 8 | HG00408.hp1 HG02523.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.726+1067G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010225 | ||||||
| chr9:27010280
|
C | T | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.726+1122C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010280 | ||||||
| chr9:27010476
|
CTTTTTTT others(7): Show |
C | 3 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026 | 3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.726+1336_726+1349d others(16): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr9 | 27010476 | |||||
| chr9:27010485
|
G | GT | 34 | a0001c0001t0001g0115a0001c0001t0001g0153a0001c0001t0001g0161others(31): Show | 34 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.726+1340dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr9 | 27010485 | |||||
| chr9:27010496
|
T | G | 1 | a0001c0001t0001g0225 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.726+1338T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010496 | ||||||
| chr9:27010552
|
C | T | 2 | a0001c0001t0010g0033a0001c0001t0010g0034 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.727-1354C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010552 | ||||||
| chr9:27010559
|
G | T | 1 | a0002c0002t0002g0060 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.727-1347G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010559 | ||||||
| chr9:27010684
|
T | G | 5 | a0007c0007t0008g0003a0007c0007t0008g0004a0007c0007t0019g0118others(2): Show | 5 | HG01255.hp2 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.727-1222T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010684 | ||||||
| chr9:27010714
|
CCCCTCGG others(3): Show |
C | 32 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(29): Show | 32 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.727-1188_727-1179d others(12): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr9 | 27010714 | |||||
| chr9:27010745
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG03490.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.727-1161G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010745 | ||||||
| chr9:27010783
|
A | G | 1 | a0005c0004t0004g0024 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.727-1123A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010783 | ||||||
| chr9:27010878
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.727-1028G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27010878 | ||||||
| chr9:27011042
|
T | A | 1 | a0001c0001t0001g0139 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.727-864T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27011042 | ||||||
| chr9:27011168
|
G | A | 2 | a0007c0007t0019g0118a0007c0007t0023g0005 | 2 | HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.727-738G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27011168 | ||||||
| chr9:27011175
|
C | G | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.727-731C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27011175 | ||||||
| chr9:27011198
|
G | A | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.727-708G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27011198 | ||||||
| chr9:27011363
|
G | T | 6 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0001g0243others(3): Show | 6 | HG01884.hp2 HG02647.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.727-543G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27011363 | ||||||
| chr9:27011369
|
T | A | 93 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0250others(90): Show | 93 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.727-537T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27011369 | ||||||
| chr9:27011387
|
C | CGTGTATG others(38): Show |
2 | a0001c0001t0003g0276a0001c0001t0003g0277 | 2 | HG01175.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.727-504_727-460dup others(45): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr9 | 27011387 | |||||
| chr9:27011396
|
A | G | 2 | a0003c0003t0002g0089a0003c0003t0002g0091 | 2 | NA19010.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.727-510A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27011396 | ||||||
| chr9:27011642
|
GAAGTTTT others(27): Show |
G | 1 | a0001c0001t0003g0294 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.727-255_727-222del others(34): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr9 | 27011642 | |||||
| chr9:27011645
|
G | GT | 6 | a0001c0001t0001g0163a0001c0001t0001g0179a0001c0001t0001g0220others(3): Show | 6 | HG00639.hp2 HG01884.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.727-243dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr9 | 27011645 | |||||
| chr9:27011645
|
GT | G | 105 | a0001c0001t0001g0142a0001c0001t0001g0227a0001c0001t0001g0229others(102): Show | 105 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.727-243delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr9 | 27011645 | |||||
| chr9:27011645
|
GTT | G | 28 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0115others(25): Show | 28 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.727-244_727-243del others(2): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr9 | 27011645 | |||||
| chr9:27011812
|
G | T | 1 | a0001c0001t0001g0259 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.727-94G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27011812 | ||||||
| chr9:27011876
|
A | G | 1 | a0001c0001t0003g0298 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.727-30A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 9/19 | chr9 | 27011876 | ||||||
| chr9:27012025
|
G | C | 8 | a0003c0003t0002g0038a0003c0003t0002g0088a0003c0003t0002g0089others(5): Show | 8 | HG00408.hp1 HG02523.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.789+57G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012025 | ||||||
| chr9:27012157
|
A | T | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+189A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012157 | ||||||
| chr9:27012326
|
G | A | 3 | a0001c0001t0003g0285a0001c0001t0003g0286a0001c0012t0003g0302 | 3 | HG00735.hp1 HG01361.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.789+358G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012326 | ||||||
| chr9:27012365
|
G | A | 27 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0115others(24): Show | 27 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.789+397G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012365 | ||||||
| chr9:27012382
|
C | G | 1 | a0001c0001t0001g0208 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.789+414C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012382 | ||||||
| chr9:27012422
|
C | T | 5 | a0001c0001t0001g0287a0001c0001t0001g0290a0001c0001t0001g0304others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.789+454C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012422 | ||||||
| chr9:27012484
|
C | T | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.789+516C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012484 | ||||||
| chr9:27012489
|
A | G | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.789+521A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012489 | ||||||
| chr9:27012498
|
A | T | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.789+530A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012498 | ||||||
| chr9:27012510
|
G | A | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.789+542G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012510 | ||||||
| chr9:27012649
|
C | G | 1 | a0001c0001t0001g0234 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.789+681C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012649 | ||||||
| chr9:27012686
|
C | G | 1 | a0007c0007t0019g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.789+718C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012686 | ||||||
| chr9:27012706
|
C | CTGTTTT | 8 | a0001c0001t0001g0115a0001c0001t0001g0119a0001c0001t0001g0121others(5): Show | 8 | HG01496.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.789+740_789+745dup others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr9 | 27012706 | |||||
| chr9:27012708
|
G | GT | 15 | a0001c0001t0001g0147a0001c0001t0001g0153a0001c0001t0001g0161others(12): Show | 15 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.789+767dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr9 | 27012708 | |||||
| chr9:27012708
|
G | GTTTTT | 40 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0252others(37): Show | 40 | HG00558.hp2 HG01081.hp2 HG01255.hp1 others(37): Show |
intron_variant | MODIFIER | c.789+763_789+767dup others(5): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr9 | 27012708 | |||||
| chr9:27012708
|
G | GTTTTTT | 37 | a0001c0001t0001g0250a0002c0002t0002g0007a0002c0002t0002g0010others(34): Show | 37 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.789+762_789+767dup others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr9 | 27012708 | |||||
| chr9:27012708
|
G | GTTTTTTT | 10 | a0002c0002t0002g0041a0002c0002t0002g0043a0002c0002t0002g0065others(7): Show | 10 | HG00408.hp1 HG03710.hp2 NA18967.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+761_789+767dup others(7): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr9 | 27012708 | |||||
| chr9:27012708
|
GT | G | 98 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(95): Show | 98 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.789+767delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr9 | 27012708 | |||||
| chr9:27012709
|
T | TTTTTG | 23 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(20): Show | 23 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.789+745_789+746ins others(5): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr9 | 27012709 | |||||
| chr9:27012723
|
T | G | 3 | a0005c0004t0004g0019a0005c0004t0004g0275a0005c0004t0036g0028 | 3 | HG01361.hp2 HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.789+755T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012723 | ||||||
| chr9:27012747
|
C | T | 1 | a0002c0002t0002g0072 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.789+779C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012747 | ||||||
| chr9:27012761
|
G | A | 1 | a0007c0007t0019g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.789+793G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012761 | ||||||
| chr9:27012766
|
G | T | 1 | a0007c0007t0019g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.789+798G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012766 | ||||||
| chr9:27012795
|
C | A | 12 | a0006c0006t0001g0325a0006c0006t0001g0326a0006c0006t0001g0327others(9): Show | 12 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.789+827C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012795 | ||||||
| chr9:27012938
|
C | T | 36 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0137others(33): Show | 36 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.789+970C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012938 | ||||||
| chr9:27012947
|
G | A | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+979G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012947 | ||||||
| chr9:27012949
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.789+981C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27012949 | ||||||
| chr9:27013073
|
A | C | 1 | a0002c0002t0002g0008 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.789+1105A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013073 | ||||||
| chr9:27013077
|
G | C | 1 | a0002c0002t0002g0101 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.789+1109G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013077 | ||||||
| chr9:27013185
|
A | G | 1 | a0001c0001t0028g0301 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.789+1217A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013185 | ||||||
| chr9:27013407
|
G | A | 1 | a0006c0006t0001g0335 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.789+1439G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013407 | ||||||
| chr9:27013426
|
G | T | 1 | a0011c0010t0017g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.789+1458G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013426 | ||||||
| chr9:27013596
|
T | G | 170 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(167): Show | 170 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(167): Show |
intron_variant | MODIFIER | c.789+1628T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013596 | ||||||
| chr9:27013627
|
A | T | 5 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 5 | HG01891.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+1659A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013627 | ||||||
| chr9:27013819
|
G | A | 1 | a0001c0001t0003g0288 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.789+1851G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013819 | ||||||
| chr9:27013883
|
T | C | 1 | a0007c0007t0019g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.789+1915T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013883 | ||||||
| chr9:27013963
|
C | T | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.789+1995C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013963 | ||||||
| chr9:27013987
|
A | G | 2 | a0001c0001t0011g0032a0001c0001t0011g0035 | 2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.789+2019A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27013987 | ||||||
| chr9:27014005
|
G | C | 1 | a0001c0001t0001g0179 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.789+2037G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014005 | ||||||
| chr9:27014006
|
G | T | 1 | a0001c0001t0001g0179 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.789+2038G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014006 | ||||||
| chr9:27014011
|
C | T | 14 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(11): Show | 14 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.789+2043C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014011 | ||||||
| chr9:27014012
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.789+2044G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014012 | ||||||
| chr9:27014013
|
A | C | 1 | a0001c0001t0001g0179 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.789+2045A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014013 | ||||||
| chr9:27014123
|
A | G | 5 | a0007c0007t0008g0003a0007c0007t0008g0004a0007c0007t0019g0118others(2): Show | 5 | HG01255.hp2 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+2155A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014123 | ||||||
| chr9:27014173
|
C | T | 5 | a0007c0007t0008g0003a0007c0007t0008g0004a0007c0007t0019g0118others(2): Show | 5 | HG01255.hp2 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+2205C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014173 | ||||||
| chr9:27014194
|
G | A | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.789+2226G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014194 | ||||||
| chr9:27014347
|
A | G | 14 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(11): Show | 14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.789+2379A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014347 | ||||||
| chr9:27014503
|
G | T | 12 | a0006c0006t0001g0325a0006c0006t0001g0326a0006c0006t0001g0327others(9): Show | 12 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.790-2404G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014503 | ||||||
| chr9:27014504
|
T | C | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.790-2403T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014504 | ||||||
| chr9:27014620
|
A | T | 12 | a0002c0002t0002g0058a0002c0002t0002g0065a0003c0003t0002g0321others(9): Show | 12 | HG00621.hp2 HG01255.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.790-2287A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014620 | ||||||
| chr9:27014636
|
G | C | 5 | a0001c0001t0007g0134a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.790-2271G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014636 | ||||||
| chr9:27014714
|
A | G | 3 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026 | 3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.790-2193A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014714 | ||||||
| chr9:27014735
|
G | A | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.790-2172G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014735 | ||||||
| chr9:27014801
|
G | T | 1 | a0001c0001t0001g0128 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.790-2106G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014801 | ||||||
| chr9:27014809
|
G | C | 88 | a0001c0001t0002g0289a0001c0001t0018g0127a0002c0002t0002g0006others(85): Show | 88 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.790-2098G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27014809 | ||||||
| chr9:27015029
|
G | A | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.790-1878G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27015029 | ||||||
| chr9:27015197
|
A | G | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.790-1710A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27015197 | ||||||
| chr9:27015241
|
T | A | 3 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026 | 3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.790-1666T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27015241 | ||||||
| chr9:27015264
|
A | C | 3 | a0001c0001t0001g0287a0001c0001t0001g0290a0001c0001t0001g0304 | 3 | HG02257.hp2 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.790-1643A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27015264 | ||||||
| chr9:27015509
|
C | T | 1 | a0002c0002t0002g0086 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.790-1398C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27015509 | ||||||
| chr9:27015605
|
C | G | 2 | a0007c0007t0019g0118a0007c0007t0023g0005 | 2 | HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.790-1302C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27015605 | ||||||
| chr9:27015727
|
T | C | 1 | a0004c0005t0005g0309 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.790-1180T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27015727 | ||||||
| chr9:27016142
|
C | A | 8 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026others(5): Show | 8 | HG00733.hp1 HG01255.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.790-765C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27016142 | ||||||
| chr9:27016337
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.790-570C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27016337 | ||||||
| chr9:27016627
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.790-280A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27016627 | ||||||
| chr9:27016652
|
C | G | 14 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(11): Show | 14 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.790-255C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27016652 | ||||||
| chr9:27016808
|
G | A | 2 | a0007c0007t0019g0118a0007c0007t0023g0005 | 2 | HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.790-99G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27016808 | ||||||
| chr9:27016833
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.790-74A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27016833 | ||||||
| chr9:27016889
|
C | G | 1 | a0007c0007t0019g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.790-18C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 10/19 | chr9 | 27016889 | ||||||
| chr9:27017138
|
A | G | 3 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026 | 3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.933+88A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27017138 | ||||||
| chr9:27017210
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.933+160C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27017210 | ||||||
| chr9:27017266
|
A | G | 1 | a0002c0002t0002g0060 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.933+216A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27017266 | ||||||
| chr9:27017318
|
C | G | 5 | a0007c0007t0008g0003a0007c0007t0008g0004a0007c0007t0019g0118others(2): Show | 5 | HG01255.hp2 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.933+268C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27017318 | ||||||
| chr9:27017755
|
G | A | 2 | a0001c0001t0015g0130a0001c0001t0015g0131 | 2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.933+705G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27017755 | ||||||
| chr9:27017961
|
G | T | 5 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0250others(2): Show | 5 | NA18988.hp2 NA18998.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.934-686G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27017961 | ||||||
| chr9:27018022
|
A | G | 171 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(168): Show | 171 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(168): Show |
intron_variant | MODIFIER | c.934-625A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27018022 | ||||||
| chr9:27018038
|
A | G | 15 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(12): Show | 15 | HG01192.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.934-609A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27018038 | ||||||
| chr9:27018221
|
A | G | 1 | a0001c0001t0033g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.934-426A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27018221 | ||||||
| chr9:27018377
|
C | A | 1 | a0001c0001t0001g0236 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.934-270C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27018377 | ||||||
| chr9:27018590
|
G | C | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.934-57G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 11/19 | chr9 | 27018590 | ||||||
| chr9:27018784
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.974+97T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27018784 | ||||||
| chr9:27019351
|
C | T | 5 | a0007c0007t0008g0003a0007c0007t0008g0004a0007c0007t0019g0118others(2): Show | 5 | HG01255.hp2 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.974+664C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27019351 | ||||||
| chr9:27019442
|
G | C | 93 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0250others(90): Show | 93 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.974+755G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27019442 | ||||||
| chr9:27019744
|
T | G | 27 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0115others(24): Show | 27 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.974+1057T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27019744 | ||||||
| chr9:27019836
|
G | A | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.974+1149G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27019836 | ||||||
| chr9:27019852
|
G | C | 94 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0250others(91): Show | 94 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.974+1165G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27019852 | ||||||
| chr9:27019873
|
A | G | 1 | a0001c0001t0003g0288 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.974+1186A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27019873 | ||||||
| chr9:27019904
|
C | A | 3 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026 | 3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.974+1217C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27019904 | ||||||
| chr9:27019976
|
A | AT | 10 | a0001c0001t0001g0260a0002c0002t0002g0045a0002c0002t0002g0068others(7): Show | 10 | HG00733.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.974+1304dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27019976 | |||||
| chr9:27019994
|
G | A | 27 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0115others(24): Show | 27 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.974+1307G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27019994 | ||||||
| chr9:27020007
|
A | G | 161 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0115others(158): Show | 161 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.974+1320A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27020007 | ||||||
| chr9:27020015
|
G | A | 1 | a0001c0001t0010g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.974+1328G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27020015 | ||||||
| chr9:27020064
|
A | T | 1 | a0001c0001t0001g0337 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.974+1377A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27020064 | ||||||
| chr9:27020244
|
T | C | 164 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0115others(161): Show | 164 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(161): Show |
intron_variant | MODIFIER | c.974+1557T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27020244 | ||||||
| chr9:27020255
|
A | G | 1 | a0006c0006t0001g0328 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.974+1568A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27020255 | ||||||
| chr9:27020474
|
T | G | 13 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0241others(10): Show | 13 | HG01257.hp2 HG01258.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.974+1787T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27020474 | ||||||
| chr9:27020560
|
C | T | 5 | a0007c0007t0008g0003a0007c0007t0008g0004a0007c0007t0019g0118others(2): Show | 5 | HG01255.hp2 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.974+1873C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27020560 | ||||||
| chr9:27020561
|
T | G | 8 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026others(5): Show | 8 | HG00733.hp1 HG01255.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.974+1874T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27020561 | ||||||
| chr9:27020826
|
G | C | 2 | a0003c0003t0002g0110a0003c0003t0002g0111 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.974+2139G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27020826 | ||||||
| chr9:27020862
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.974+2175G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27020862 | ||||||
| chr9:27021173
|
A | G | 3 | a0001c0001t0010g0033a0001c0001t0011g0032a0001c0001t0011g0035 | 3 | HG02451.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.974+2486A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021173 | ||||||
| chr9:27021239
|
G | A | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.974+2552G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021239 | ||||||
| chr9:27021372
|
T | G | 1 | a0001c0001t0001g0189 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.974+2685T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021372 | ||||||
| chr9:27021458
|
A | T | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.974+2771A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021458 | ||||||
| chr9:27021550
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.974+2863T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021550 | ||||||
| chr9:27021584
|
G | A | 2 | a0007c0007t0019g0118a0007c0007t0023g0005 | 2 | HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.974+2897G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021584 | ||||||
| chr9:27021618
|
G | A | 1 | a0001c0001t0010g0033 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.974+2931G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021618 | ||||||
| chr9:27021770
|
A | G | 1 | a0001c0001t0035g0242 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.974+3083A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021770 | ||||||
| chr9:27021952
|
G | A | 1 | a0001c0001t0003g0294 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.974+3265G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021952 | ||||||
| chr9:27021995
|
A | C | 94 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0250others(91): Show | 94 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.974+3308A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021995 | ||||||
| chr9:27021996
|
T | G | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3309T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021996 | ||||||
| chr9:27021997
|
T | C | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3310T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27021997 | ||||||
| chr9:27022002
|
T | A | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3315T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022002 | ||||||
| chr9:27022003
|
T | G | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3316T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022003 | ||||||
| chr9:27022007
|
A | G | 28 | a0001c0001t0001g0240a0001c0001t0003g0272a0001c0001t0003g0273others(25): Show | 28 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.974+3320A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022007 | ||||||
| chr9:27022008
|
T | TCTCTCTC others(25): Show |
1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3321_974+3322i others(34): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022008 | ||||||
| chr9:27022021
|
G | C | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3334G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022021 | ||||||
| chr9:27022022
|
A | T | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3335A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022022 | ||||||
| chr9:27022023
|
G | A | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3336G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022023 | ||||||
| chr9:27022028
|
C | G | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3341C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022028 | ||||||
| chr9:27022029
|
A | C | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3342A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022029 | ||||||
| chr9:27022032
|
T | G | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3345T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022032 | ||||||
| chr9:27022038
|
CTCCTACT others(43): Show |
C | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3356_974+3405d others(52): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27022038 | |||||
| chr9:27022061
|
A | T | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.974+3374A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022061 | ||||||
| chr9:27022091
|
C | T | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3404C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022091 | ||||||
| chr9:27022097
|
C | T | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3410C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022097 | ||||||
| chr9:27022099
|
A | T | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3412A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022099 | ||||||
| chr9:27022103
|
T | G | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3416T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022103 | ||||||
| chr9:27022104
|
A | T | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3417A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022104 | ||||||
| chr9:27022109
|
T | G | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3422T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022109 | ||||||
| chr9:27022112
|
T | G | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3425T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022112 | ||||||
| chr9:27022115
|
G | GAGAGAGA others(4): Show |
1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3428_974+3429i others(13): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022115 | ||||||
| chr9:27022118
|
T | A | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3431T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022118 | ||||||
| chr9:27022119
|
T | G | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3432T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022119 | ||||||
| chr9:27022120
|
T | A | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3433T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022120 | ||||||
| chr9:27022124
|
A | G | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3437A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022124 | ||||||
| chr9:27022125
|
A | T | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3438A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022125 | ||||||
| chr9:27022126
|
G | T | 1 | a0002c0002t0002g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974+3439G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022126 | ||||||
| chr9:27022241
|
T | C | 1 | a0002c0002t0002g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.974+3554T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022241 | ||||||
| chr9:27022319
|
C | T | 25 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0115others(22): Show | 25 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.974+3632C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022319 | ||||||
| chr9:27022343
|
G | C | 3 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026 | 3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.974+3656G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022343 | ||||||
| chr9:27022507
|
G | A | 5 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0008g0003others(2): Show | 5 | HG02615.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.974+3820G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022507 | ||||||
| chr9:27022516
|
T | G | 5 | a0001c0001t0007g0134a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.974+3829T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022516 | ||||||
| chr9:27022646
|
C | CT | 127 | a0001c0001t0001g0102a0001c0001t0001g0108a0001c0001t0001g0115others(124): Show | 127 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.974+3973dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27022646 | |||||
| chr9:27022646
|
CT | C | 9 | a0001c0001t0001g0258a0001c0001t0003g0281a0001c0001t0009g0030others(6): Show | 9 | HG00140.hp1 HG01255.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.974+3973delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27022646 | |||||
| chr9:27022803
|
G | A | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.974+4116G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022803 | ||||||
| chr9:27022887
|
C | T | 1 | a0003c0003t0002g0037 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.974+4200C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022887 | ||||||
| chr9:27022919
|
T | C | 5 | a0001c0001t0007g0134a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.974+4232T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022919 | ||||||
| chr9:27022938
|
G | A | 28 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(25): Show | 28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.974+4251G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27022938 | ||||||
| chr9:27023006
|
A | G | 2 | a0007c0007t0019g0118a0007c0007t0023g0005 | 2 | HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.974+4319A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27023006 | ||||||
| chr9:27023110
|
A | G | 1 | a0011c0010t0017g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.974+4423A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27023110 | ||||||
| chr9:27023265
|
C | T | 10 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0006g0016others(7): Show | 10 | HG00733.hp1 HG01255.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.974+4578C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27023265 | ||||||
| chr9:27023287
|
C | T | 2 | a0001c0001t0010g0033a0001c0001t0010g0034 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.974+4600C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27023287 | ||||||
| chr9:27023343
|
A | G | 1 | a0002c0002t0002g0095 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.974+4656A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27023343 | ||||||
| chr9:27023560
|
A | AT | 13 | a0002c0002t0002g0068a0006c0006t0001g0325a0006c0006t0001g0326others(10): Show | 13 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.974+4882dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27023560 | |||||
| chr9:27023581
|
C | T | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.974+4894C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27023581 | ||||||
| chr9:27023596
|
G | A | 1 | a0002c0002t0002g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.974+4909G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27023596 | ||||||
| chr9:27023620
|
T | G | 97 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0232others(94): Show | 97 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.974+4933T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27023620 | ||||||
| chr9:27023941
|
A | T | 1 | a0003c0003t0027g0098 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.975-5084A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27023941 | ||||||
| chr9:27024179
|
A | G | 93 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0250others(90): Show | 93 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.975-4846A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27024179 | ||||||
| chr9:27024347
|
G | T | 1 | a0001c0001t0010g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.975-4678G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27024347 | ||||||
| chr9:27024419
|
A | G | 2 | a0001c0001t0011g0032a0001c0001t0011g0035 | 2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.975-4606A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27024419 | ||||||
| chr9:27024452
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.975-4573T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27024452 | ||||||
| chr9:27024517
|
A | C | 1 | a0003c0003t0002g0097 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.975-4508A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27024517 | ||||||
| chr9:27024791
|
A | G | 3 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026 | 3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.975-4234A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27024791 | ||||||
| chr9:27024974
|
T | TA | 10 | a0001c0001t0001g0151a0001c0001t0009g0030a0001c0001t0009g0031others(7): Show | 10 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.975-4037dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27024974 | |||||
| chr9:27024974
|
T | TAA | 11 | a0006c0006t0001g0325a0006c0006t0001g0326a0006c0006t0001g0327others(8): Show | 11 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.975-4038_975-4037d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27024974 | |||||
| chr9:27024974
|
TA | T | 7 | a0001c0001t0001g0146a0001c0001t0001g0153a0001c0001t0001g0161others(4): Show | 7 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.975-4037delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27024974 | |||||
| chr9:27024989
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0034g0140 | 3 | HG01099.hp2 HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.975-4036G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27024989 | ||||||
| chr9:27025019
|
G | A | 7 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0008g0003others(4): Show | 7 | HG01255.hp2 HG02615.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.975-4006G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025019 | ||||||
| chr9:27025156
|
A | G | 1 | a0001c0001t0033g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.975-3869A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025156 | ||||||
| chr9:27025313
|
C | T | 1 | a0001c0001t0007g0170 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.975-3712C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025313 | ||||||
| chr9:27025423
|
A | G | 12 | a0006c0006t0001g0325a0006c0006t0001g0326a0006c0006t0001g0327others(9): Show | 12 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.975-3602A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025423 | ||||||
| chr9:27025429
|
T | C | 97 | a0001c0001t0009g0030a0001c0001t0009g0031a0001c0001t0018g0127others(94): Show | 97 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.975-3596T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025429 | ||||||
| chr9:27025443
|
C | CA | 42 | a0001c0001t0001g0154a0001c0001t0001g0158a0001c0001t0001g0165others(39): Show | 42 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.975-3562dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27025443 | |||||
| chr9:27025443
|
CA | C | 113 | a0001c0001t0001g0129a0001c0001t0010g0033a0001c0001t0010g0034others(110): Show | 113 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.975-3562delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27025443 | |||||
| chr9:27025443
|
CAA | C | 13 | a0002c0002t0002g0047a0002c0002t0002g0048a0002c0002t0002g0055others(10): Show | 13 | HG00639.hp1 HG01081.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.975-3563_975-3562d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27025443 | |||||
| chr9:27025459
|
A | G | 6 | a0001c0001t0001g0226a0001c0001t0009g0030a0001c0001t0009g0031others(3): Show | 6 | HG02615.hp1 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.975-3566A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025459 | ||||||
| chr9:27025460
|
A | G | 28 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(25): Show | 28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.975-3565A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025460 | ||||||
| chr9:27025495
|
A | C | 10 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0006g0016others(7): Show | 10 | HG00733.hp1 HG01255.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.975-3530A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025495 | ||||||
| chr9:27025533
|
T | C | 1 | a0002c0002t0002g0075 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.975-3492T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025533 | ||||||
| chr9:27025691
|
C | T | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.975-3334C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025691 | ||||||
| chr9:27025854
|
C | T | 7 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0008g0003others(4): Show | 7 | HG01255.hp2 HG02615.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.975-3171C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025854 | ||||||
| chr9:27025976
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.975-3049A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27025976 | ||||||
| chr9:27026044
|
G | A | 1 | a0004c0005t0005g0310 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.975-2981G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026044 | ||||||
| chr9:27026132
|
G | C | 6 | a0001c0001t0001g0102a0001c0001t0001g0115a0001c0001t0001g0116others(3): Show | 6 | HG01192.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.975-2893G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026132 | ||||||
| chr9:27026144
|
T | A | 163 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0115others(160): Show | 163 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.975-2881T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026144 | ||||||
| chr9:27026192
|
T | C | 1 | a0001c0001t0018g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.975-2833T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026192 | ||||||
| chr9:27026375
|
A | G | 3 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026 | 3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.975-2650A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026375 | ||||||
| chr9:27026417
|
C | T | 7 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0008g0003others(4): Show | 7 | HG01255.hp2 HG02615.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.975-2608C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026417 | ||||||
| chr9:27026490
|
T | C | 1 | a0002c0002t0002g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.975-2535T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026490 | ||||||
| chr9:27026572
|
G | A | 1 | a0001c0001t0001g0338 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.975-2453G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026572 | ||||||
| chr9:27026658
|
A | C | 6 | a0001c0001t0001g0107a0001c0001t0009g0030a0001c0001t0009g0031others(3): Show | 6 | HG02615.hp1 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.975-2367A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026658 | ||||||
| chr9:27026706
|
A | T | 1 | a0001c0001t0001g0164 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.975-2319A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026706 | ||||||
| chr9:27026829
|
C | T | 10 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0006g0016others(7): Show | 10 | HG00733.hp1 HG01255.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.975-2196C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026829 | ||||||
| chr9:27026830
|
T | G | 10 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0006g0016others(7): Show | 10 | HG00733.hp1 HG01255.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.975-2195T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026830 | ||||||
| chr9:27026846
|
G | T | 1 | a0002c0002t0002g0093 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.975-2179G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026846 | ||||||
| chr9:27026859
|
A | G | 4 | a0001c0001t0001g0102a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG01192.hp1 HG02280.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.975-2166A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026859 | ||||||
| chr9:27026899
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.975-2126G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026899 | ||||||
| chr9:27026959
|
AG | A | 340 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(337): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.975-2064delG | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 27026959 | |||||
| chr9:27026966
|
T | A | 340 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(337): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.975-2059T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27026966 | ||||||
| chr9:27027054
|
A | C | 1 | a0006c0006t0001g0335 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.975-1971A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27027054 | ||||||
| chr9:27027146
|
C | G | 17 | a0002c0002t0002g0051a0002c0002t0002g0058a0002c0002t0002g0076others(14): Show | 17 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.975-1879C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27027146 | ||||||
| chr9:27027242
|
T | C | 34 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(31): Show | 34 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.975-1783T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27027242 | ||||||
| chr9:27027414
|
T | C | 1 | a0001c0001t0018g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.975-1611T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27027414 | ||||||
| chr9:27027808
|
A | G | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.975-1217A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27027808 | ||||||
| chr9:27027867
|
T | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0034g0140 | 3 | HG01099.hp2 HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.975-1158T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27027867 | ||||||
| chr9:27027940
|
G | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG01496.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.975-1085G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27027940 | ||||||
| chr9:27028163
|
T | A | 2 | a0003c0003t0002g0042a0003c0003t0002g0049 | 2 | HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.975-862T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028163 | ||||||
| chr9:27028292
|
C | G | 5 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 5 | HG01891.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.975-733C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028292 | ||||||
| chr9:27028383
|
G | C | 1 | a0011c0010t0017g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.975-642G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028383 | ||||||
| chr9:27028384
|
G | C | 3 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026 | 3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.975-641G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028384 | ||||||
| chr9:27028433
|
G | A | 2 | a0001c0001t0018g0127a0011c0010t0017g0114 | 2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.975-592G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028433 | ||||||
| chr9:27028625
|
G | A | 3 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121 | 3 | HG03041.hp1 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.975-400G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028625 | ||||||
| chr9:27028669
|
T | C | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.975-356T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028669 | ||||||
| chr9:27028680
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.975-345C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028680 | ||||||
| chr9:27028720
|
A | C | 339 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(336): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.975-305A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028720 | ||||||
| chr9:27028891
|
T | C | 2 | a0001c0001t0001g0158a0001c0001t0029g0157 | 2 | HG00423.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.975-134T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028891 | ||||||
| chr9:27028949
|
A | G | 32 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0137others(29): Show | 32 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.975-76A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 12/19 | chr9 | 27028949 | ||||||
| chr9:27029107
|
A | T | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
splice_region_variant&intron_variant | LOW | c.1054+3A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029107 | ||||||
| chr9:27029249
|
A | T | 2 | a0001c0001t0003g0299a0001c0001t0003g0300 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1054+145A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029249 | ||||||
| chr9:27029250
|
C | T | 2 | a0001c0001t0003g0299a0001c0001t0003g0300 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1054+146C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029250 | ||||||
| chr9:27029386
|
G | C | 1 | a0001c0001t0001g0264 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1054+282G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029386 | ||||||
| chr9:27029531
|
G | A | 1 | a0002c0002t0002g0071 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1054+427G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029531 | ||||||
| chr9:27029538
|
G | A | 4 | a0002c0002t0002g0071a0007c0007t0008g0003a0007c0007t0008g0004others(1): Show | 4 | HG01346.hp2 HG02615.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1054+434G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029538 | ||||||
| chr9:27029605
|
G | A | 28 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(25): Show | 28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1054+501G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029605 | ||||||
| chr9:27029615
|
G | A | 2 | a0001c0001t0001g0263a0001c0001t0001g0270 | 2 | NA18747.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1054+511G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029615 | ||||||
| chr9:27029641
|
G | A | 159 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0115others(156): Show | 159 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.1054+537G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029641 | ||||||
| chr9:27029688
|
C | T | 89 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(86): Show | 89 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.1054+584C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029688 | ||||||
| chr9:27029750
|
A | G | 1 | a0001c0001t0007g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1054+646A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029750 | ||||||
| chr9:27029825
|
T | C | 7 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0008g0003others(4): Show | 7 | HG01255.hp2 HG02615.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1054+721T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029825 | ||||||
| chr9:27029889
|
G | A | 7 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0008g0003others(4): Show | 7 | HG01255.hp2 HG02615.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1054+785G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27029889 | ||||||
| chr9:27030007
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1054+903A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030007 | ||||||
| chr9:27030013
|
T | C | 3 | a0007c0007t0006g0016a0007c0007t0006g0025a0007c0007t0006g0026 | 3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1054+909T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030013 | ||||||
| chr9:27030124
|
C | G | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1054+1020C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030124 | ||||||
| chr9:27030153
|
G | A | 3 | a0002c0002t0002g0029a0002c0002t0002g0044a0002c0002t0002g0045 | 3 | HG00597.hp1 NA18988.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1054+1049G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030153 | ||||||
| chr9:27030235
|
A | G | 1 | a0002c0002t0002g0060 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1054+1131A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030235 | ||||||
| chr9:27030291
|
A | G | 5 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0008g0003others(2): Show | 5 | HG02615.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054+1187A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030291 | ||||||
| chr9:27030350
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1054+1246C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030350 | ||||||
| chr9:27030420
|
T | G | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1054+1316T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030420 | ||||||
| chr9:27030479
|
C | T | 32 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(29): Show | 32 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1054+1375C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030479 | ||||||
| chr9:27030542
|
C | T | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1054+1438C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030542 | ||||||
| chr9:27030547
|
C | CA | 191 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0136others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1054+1461dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27030547 | |||||
| chr9:27030547
|
C | CAA | 103 | a0001c0001t0001g0135a0001c0001t0001g0208a0001c0001t0001g0229others(100): Show | 103 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1054+1460_1054+146 others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27030547 | |||||
| chr9:27030547
|
CA | C | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(14): Show | 17 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1054+1461delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27030547 | |||||
| chr9:27030790
|
T | A | 2 | a0007c0007t0019g0118a0007c0007t0023g0005 | 2 | HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1054+1686T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030790 | ||||||
| chr9:27030840
|
A | G | 1 | a0005c0004t0004g0014 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1054+1736A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030840 | ||||||
| chr9:27030858
|
G | T | 1 | a0001c0001t0010g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1054+1754G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030858 | ||||||
| chr9:27030929
|
A | G | 2 | a0001c0001t0003g0293a0001c0001t0003g0296 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1054+1825A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27030929 | ||||||
| chr9:27031283
|
G | T | 1 | a0001c0001t0001g0178 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1054+2179G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031283 | ||||||
| chr9:27031302
|
TA | T | 10 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0006g0016others(7): Show | 10 | HG00733.hp1 HG01255.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1054+2204delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031302 | |||||
| chr9:27031318
|
T | C | 2 | a0003c0003t0002g0110a0003c0003t0002g0111 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1054+2214T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031318 | ||||||
| chr9:27031392
|
A | G | 10 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0006g0016others(7): Show | 10 | HG00733.hp1 HG01255.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1054+2288A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031392 | ||||||
| chr9:27031461
|
C | G | 5 | a0001c0001t0007g0134a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG01074.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054+2357C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031461 | ||||||
| chr9:27031462
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0153others(6): Show | 9 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1054+2358G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031462 | ||||||
| chr9:27031485
|
C | T | 91 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0250others(88): Show | 91 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.1054+2381C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031485 | ||||||
| chr9:27031510
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1054+2406C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031510 | ||||||
| chr9:27031549
|
A | G | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1054+2445A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031549 | ||||||
| chr9:27031560
|
C | T | 5 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0008g0003others(2): Show | 5 | HG02615.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054+2456C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031560 | ||||||
| chr9:27031576
|
A | G | 1 | a0004c0005t0005g0310 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1054+2472A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031576 | ||||||
| chr9:27031597
|
A | AT | 31 | a0001c0001t0001g0108a0001c0001t0001g0240a0001c0001t0003g0272others(28): Show | 31 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.1054+2510dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031597 | |||||
| chr9:27031597
|
AT | A | 15 | a0001c0001t0001g0102a0001c0001t0001g0115a0001c0001t0001g0116others(12): Show | 15 | HG01070.hp1 HG01192.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1054+2510delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031597 | |||||
| chr9:27031604
|
T | C | 2 | a0003c0003t0002g0110a0003c0003t0002g0111 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1054+2500T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031604 | ||||||
| chr9:27031620
|
G | GA | 3 | a0001c0001t0001g0225a0001c0001t0001g0231a0001c0001t0001g0306 | 3 | HG01243.hp1 HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1054+2517dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031620 | |||||
| chr9:27031667
|
A | C | 1 | a0003c0003t0002g0324 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1054+2563A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031667 | ||||||
| chr9:27031732
|
T | TAAATA | 77 | a0001c0001t0001g0121a0001c0001t0001g0141a0001c0001t0001g0151others(74): Show | 77 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1054+2676_1054+268 others(9): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031732 | |||||
| chr9:27031732
|
T | TAAATAAA others(3): Show |
57 | a0001c0001t0001g0129a0001c0001t0001g0149a0001c0001t0001g0187others(54): Show | 57 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1054+2671_1054+268 others(14): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031732 | |||||
| chr9:27031732
|
T | TAAATAAA others(8): Show |
13 | a0001c0001t0001g0213a0001c0008t0001g0168a0002c0002t0002g0029others(10): Show | 13 | HG00558.hp2 HG00735.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.1054+2666_1054+268 others(19): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031732 | |||||
| chr9:27031732
|
T | TAAATAAA others(13): Show |
1 | a0002c0002t0002g0036 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1054+2661_1054+268 others(24): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031732 | |||||
| chr9:27031732
|
TAAATA | T | 60 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0128others(57): Show | 60 | HG00558.hp1 HG00609.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.1054+2676_1054+268 others(9): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031732 | |||||
| chr9:27031732
|
TAAATAAA others(3): Show |
T | 18 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0163others(15): Show | 18 | HG00323.hp2 HG00408.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1054+2671_1054+268 others(14): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031732 | |||||
| chr9:27031781
|
T | TAAAATAA others(4): Show |
1 | a0002c0002t0002g0039 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1054+2680_1054+268 others(15): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031781 | |||||
| chr9:27031781
|
TAAATAAA others(15): Show |
T | 1 | a0001c0001t0003g0294 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1054+2702_1054+272 others(26): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27031781 | |||||
| chr9:27031782
|
AAATAAAA others(7): Show |
A | 2 | a0007c0007t0006g0016a0007c0007t0006g0026 | 2 | HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1054+2679_1054+269 others(18): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031782 | ||||||
| chr9:27031796
|
G | A | 8 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0006g0025others(5): Show | 8 | HG00733.hp1 HG01255.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1054+2692G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031796 | ||||||
| chr9:27031843
|
G | C | 14 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(11): Show | 14 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1054+2739G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031843 | ||||||
| chr9:27031897
|
G | A | 159 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0115others(156): Show | 159 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.1054+2793G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031897 | ||||||
| chr9:27031921
|
A | G | 1 | a0001c0001t0002g0289 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1054+2817A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031921 | ||||||
| chr9:27031925
|
T | C | 2 | a0003c0003t0002g0110a0003c0003t0002g0111 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1054+2821T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031925 | ||||||
| chr9:27031972
|
A | G | 1 | a0001c0001t0025g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1054+2868A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27031972 | ||||||
| chr9:27032316
|
T | G | 1 | a0005c0004t0004g0014 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1054+3212T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032316 | ||||||
| chr9:27032320
|
A | G | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0115others(5): Show | 8 | HG01192.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1054+3216A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032320 | ||||||
| chr9:27032334
|
G | A | 27 | a0001c0001t0003g0272a0001c0001t0003g0273a0001c0001t0003g0274others(24): Show | 27 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.1054+3230G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032334 | ||||||
| chr9:27032339
|
C | T | 86 | a0001c0001t0002g0289a0001c0001t0018g0127a0002c0002t0002g0006others(83): Show | 86 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1054+3235C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032339 | ||||||
| chr9:27032387
|
G | A | 130 | a0001c0001t0002g0289a0001c0001t0009g0030a0001c0001t0009g0031others(127): Show | 130 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.1054+3283G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032387 | ||||||
| chr9:27032532
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1054+3428A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032532 | ||||||
| chr9:27032569
|
T | TA | 25 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0115others(22): Show | 25 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.1054+3474dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27032569 | |||||
| chr9:27032622
|
C | A | 5 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0008g0003others(2): Show | 5 | HG02615.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054+3518C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032622 | ||||||
| chr9:27032791
|
G | A | 1 | a0006c0006t0026g0206 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1054+3687G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032791 | ||||||
| chr9:27032810
|
A | G | 7 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0008g0003others(4): Show | 7 | HG01255.hp2 HG02615.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1054+3706A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032810 | ||||||
| chr9:27032821
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1054+3717G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032821 | ||||||
| chr9:27032827
|
C | T | 5 | a0003c0003t0006g0112a0003c0003t0006g0113a0007c0007t0006g0016others(2): Show | 5 | HG00733.hp1 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054+3723C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032827 | ||||||
| chr9:27032914
|
T | G | 2 | a0007c0007t0019g0118a0007c0007t0023g0005 | 2 | HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1054+3810T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032914 | ||||||
| chr9:27032923
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1054+3819C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032923 | ||||||
| chr9:27032964
|
G | A | 270 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(267): Show | 270 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.1054+3860G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27032964 | ||||||
| chr9:27033210
|
C | A | 1 | a0004c0005t0005g0315 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1054+4106C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033210 | ||||||
| chr9:27033328
|
G | C | 1 | a0007c0007t0019g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1054+4224G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033328 | ||||||
| chr9:27033401
|
A | AG | 3 | a0001c0001t0003g0291a0001c0001t0003g0303a0012c0014t0003g0282 | 3 | HG01952.hp1 HG01978.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1054+4297_1054+429 others(5): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033401 | ||||||
| chr9:27033403
|
AC | A | 5 | a0003c0003t0006g0112a0003c0003t0006g0113a0007c0007t0006g0016others(2): Show | 5 | HG00733.hp1 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054+4300delC | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033403 | ||||||
| chr9:27033560
|
T | C | 1 | a0004c0005t0005g0315 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1054+4456T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033560 | ||||||
| chr9:27033573
|
C | CA | 20 | a0001c0001t0001g0107a0001c0001t0001g0164a0001c0001t0001g0165others(17): Show | 20 | HG01123.hp1 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1054+4490dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27033573 | |||||
| chr9:27033573
|
C | CAA | 14 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(11): Show | 14 | HG00639.hp2 HG01256.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1054+4489_1054+449 others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27033573 | |||||
| chr9:27033573
|
C | CAAAA | 12 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(9): Show | 12 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.1054+4487_1054+449 others(8): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27033573 | |||||
| chr9:27033573
|
CA | C | 8 | a0001c0001t0001g0188a0001c0001t0001g0231a0001c0001t0001g0238others(5): Show | 8 | HG00733.hp1 HG01070.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1054+4490delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27033573 | |||||
| chr9:27033609
|
C | T | 7 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0008g0003others(4): Show | 7 | HG01255.hp2 HG02615.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1054+4505C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033609 | ||||||
| chr9:27033643
|
A | G | 3 | a0001c0001t0001g0184a0001c0001t0001g0192a0001c0001t0001g0193 | 3 | NA18612.hp1 NA18980.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1054+4539A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033643 | ||||||
| chr9:27033649
|
G | A | 2 | a0001c0001t0003g0299a0001c0001t0003g0300 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1054+4545G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033649 | ||||||
| chr9:27033702
|
T | A | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054+4598T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033702 | ||||||
| chr9:27033744
|
A | AT | 12 | a0001c0001t0009g0030a0001c0001t0009g0031a0003c0003t0006g0112others(9): Show | 12 | HG00733.hp1 HG01255.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1054+4641dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27033744 | |||||
| chr9:27033851
|
G | T | 1 | a0001c0001t0018g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1054+4747G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033851 | ||||||
| chr9:27033929
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1054+4825C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033929 | ||||||
| chr9:27033962
|
C | T | 4 | a0002c0002t0002g0122a0002c0002t0002g0123a0002c0002t0002g0124others(1): Show | 4 | NA18991.hp2 NA19002.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054+4858C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27033962 | ||||||
| chr9:27034108
|
C | T | 1 | a0004c0005t0005g0313 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1054+5004C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27034108 | ||||||
| chr9:27034152
|
T | C | 5 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 5 | HG01891.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054+5048T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27034152 | ||||||
| chr9:27034291
|
A | C | 1 | a0002c0002t0002g0058 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1054+5187A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27034291 | ||||||
| chr9:27034356
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1054+5252A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27034356 | ||||||
| chr9:27034515
|
T | C | 12 | a0006c0006t0001g0325a0006c0006t0001g0326a0006c0006t0001g0327others(9): Show | 12 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1054+5411T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27034515 | ||||||
| chr9:27034721
|
G | A | 1 | a0007c0007t0019g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1054+5617G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27034721 | ||||||
| chr9:27034883
|
T | C | 1 | a0002c0002t0002g0083 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1054+5779T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27034883 | ||||||
| chr9:27034972
|
T | C | 3 | a0004c0005t0005g0314a0004c0005t0005g0316a0004c0005t0005g0318 | 3 | NA18957.hp1 NA18965.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1054+5868T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27034972 | ||||||
| chr9:27035013
|
G | A | 5 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0008g0003others(2): Show | 5 | HG02615.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054+5909G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27035013 | ||||||
| chr9:27035167
|
G | A | 1 | a0007c0007t0019g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1054+6063G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27035167 | ||||||
| chr9:27035246
|
G | A | 9 | a0001c0001t0001g0129a0001c0001t0001g0258a0001c0001t0009g0030others(6): Show | 9 | HG01255.hp2 HG01496.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1054+6142G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27035246 | ||||||
| chr9:27035907
|
G | A | 2 | a0001c0001t0018g0127a0011c0010t0017g0114 | 2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1054+6803G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27035907 | ||||||
| chr9:27036023
|
C | T | 1 | a0003c0003t0006g0113 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1054+6919C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27036023 | ||||||
| chr9:27036067
|
C | A | 1 | a0007c0007t0019g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1054+6963C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27036067 | ||||||
| chr9:27036143
|
G | C | 2 | a0001c0001t0003g0299a0001c0001t0003g0300 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1054+7039G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27036143 | ||||||
| chr9:27036200
|
A | C | 1 | a0001c0001t0001g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1054+7096A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27036200 | ||||||
| chr9:27036404
|
T | A | 1 | a0001c0001t0018g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1054+7300T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27036404 | ||||||
| chr9:27036411
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1054+7307A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27036411 | ||||||
| chr9:27036475
|
A | G | 6 | a0001c0001t0001g0107a0001c0001t0009g0030a0001c0001t0009g0031others(3): Show | 6 | HG02615.hp1 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1054+7371A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27036475 | ||||||
| chr9:27036489
|
C | T | 2 | a0001c0001t0001g0337a0001c0001t0001g0339 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1054+7385C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27036489 | ||||||
| chr9:27036806
|
G | A | 12 | a0001c0001t0009g0030a0001c0001t0009g0031a0003c0003t0006g0112others(9): Show | 12 | HG00733.hp1 HG01255.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1054+7702G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27036806 | ||||||
| chr9:27037076
|
C | T | 1 | a0006c0006t0026g0206 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1055-7666C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27037076 | ||||||
| chr9:27037093
|
A | G | 180 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(177): Show | 180 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(177): Show |
intron_variant | MODIFIER | c.1055-7649A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27037093 | ||||||
| chr9:27037220
|
C | CA | 95 | a0001c0001t0001g0107a0001c0001t0001g0198a0001c0001t0001g0229others(92): Show | 95 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.1055-7503dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27037220 | |||||
| chr9:27037220
|
CA | C | 146 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0135others(143): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.1055-7503delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27037220 | |||||
| chr9:27037555
|
G | A | 2 | a0004c0005t0005g0308a0004c0005t0005g0309 | 2 | HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1055-7187G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27037555 | ||||||
| chr9:27037760
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1055-6982A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27037760 | ||||||
| chr9:27037804
|
T | C | 2 | a0001c0001t0018g0127a0011c0010t0017g0114 | 2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1055-6938T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27037804 | ||||||
| chr9:27037983
|
T | C | 1 | a0009c0011t0001g0235 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1055-6759T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27037983 | ||||||
| chr9:27038055
|
C | T | 1 | a0007c0007t0006g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1055-6687C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038055 | ||||||
| chr9:27038088
|
T | C | 4 | a0001c0001t0010g0033a0001c0001t0010g0034a0001c0001t0011g0032others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1055-6654T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038088 | ||||||
| chr9:27038128
|
G | T | 2 | a0001c0001t0001g0151a0001c0001t0020g0150 | 2 | HG02056.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1055-6614G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038128 | ||||||
| chr9:27038176
|
A | G | 1 | a0003c0003t0002g0087 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1055-6566A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038176 | ||||||
| chr9:27038229
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1055-6513T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038229 | ||||||
| chr9:27038375
|
G | A | 2 | a0007c0007t0019g0118a0007c0007t0023g0005 | 2 | HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1055-6367G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038375 | ||||||
| chr9:27038470
|
C | G | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055-6272C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038470 | ||||||
| chr9:27038576
|
C | A | 5 | a0003c0003t0006g0112a0003c0003t0006g0113a0007c0007t0006g0016others(2): Show | 5 | HG00733.hp1 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055-6166C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038576 | ||||||
| chr9:27038644
|
C | T | 1 | a0006c0006t0026g0206 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1055-6098C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038644 | ||||||
| chr9:27038753
|
A | T | 1 | a0007c0007t0019g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1055-5989A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038753 | ||||||
| chr9:27038789
|
A | G | 6 | a0001c0001t0001g0107a0001c0001t0009g0030a0001c0001t0009g0031others(3): Show | 6 | HG02615.hp1 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1055-5953A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038789 | ||||||
| chr9:27038939
|
A | G | 1 | a0002c0002t0002g0101 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1055-5803A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038939 | ||||||
| chr9:27038950
|
T | G | 91 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0250others(88): Show | 91 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.1055-5792T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27038950 | ||||||
| chr9:27039006
|
T | C | 2 | a0001c0001t0010g0033a0001c0001t0010g0034 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1055-5736T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27039006 | ||||||
| chr9:27039019
|
C | T | 1 | a0002c0002t0002g0083 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1055-5723C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27039019 | ||||||
| chr9:27039251
|
G | A | 1 | a0002c0002t0002g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1055-5491G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27039251 | ||||||
| chr9:27039256
|
C | T | 2 | a0001c0001t0001g0237a0001c0001t0001g0251 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1055-5486C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27039256 | ||||||
| chr9:27039348
|
G | C | 2 | a0001c0001t0015g0130a0001c0001t0015g0131 | 2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1055-5394G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27039348 | ||||||
| chr9:27039450
|
A | G | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055-5292A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27039450 | ||||||
| chr9:27039689
|
G | C | 1 | a0002c0002t0002g0060 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1055-5053G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27039689 | ||||||
| chr9:27039728
|
C | A | 1 | a0001c0001t0033g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1055-5014C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27039728 | ||||||
| chr9:27039982
|
G | A | 2 | a0001c0001t0015g0130a0001c0001t0015g0131 | 2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1055-4760G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27039982 | ||||||
| chr9:27040256
|
T | C | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1055-4486T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27040256 | ||||||
| chr9:27040299
|
C | T | 1 | a0001c0001t0010g0033 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1055-4443C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27040299 | ||||||
| chr9:27040544
|
C | CA | 23 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(20): Show | 23 | HG01069.hp1 HG01074.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1055-4175dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | |||||
| chr9:27040544
|
C | CAA | 77 | a0001c0001t0001g0250a0001c0001t0001g0252a0001c0001t0001g0255others(74): Show | 77 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.1055-4176_1055-417 others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | |||||
| chr9:27040544
|
C | CAAA | 12 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0002g0183others(9): Show | 12 | HG01884.hp1 HG01978.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1055-4177_1055-417 others(7): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | |||||
| chr9:27040544
|
C | CAAAAA | 21 | a0004c0005t0005g0310a0004c0005t0005g0312a0004c0005t0005g0314others(18): Show | 21 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.1055-4179_1055-417 others(9): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | |||||
| chr9:27040544
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0009g0030 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1055-4188_1055-417 others(18): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | |||||
| chr9:27040544
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0009g0031 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1055-4189_1055-417 others(19): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | |||||
| chr9:27040544
|
C | CAAAAAAA others(9): Show |
2 | a0003c0003t0002g0323a0003c0003t0002g0324 | 2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1055-4190_1055-417 others(20): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | |||||
| chr9:27040544
|
C | CAAAAAAA others(10): Show |
2 | a0003c0003t0002g0321a0003c0003t0002g0322 | 2 | HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1055-4191_1055-417 others(21): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | |||||
| chr9:27040544
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0011g0032 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1055-4175_1055-417 others(29): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | |||||
| chr9:27040544
|
C | CAAAAAAA others(29): Show |
1 | a0001c0001t0010g0033 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1055-4175_1055-417 others(40): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | |||||
| chr9:27040544
|
CA | C | 10 | a0001c0001t0001g0136a0001c0001t0001g0158a0001c0001t0001g0177others(7): Show | 10 | HG00323.hp1 HG00423.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.1055-4175delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | |||||
| chr9:27040544
|
CAAAAAAA | C | 6 | a0003c0003t0006g0112a0003c0003t0006g0113a0007c0007t0006g0016others(3): Show | 6 | HG00733.hp1 HG01255.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1055-4181_1055-417 others(11): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27040544 | |||||
| chr9:27040576
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1055-4166G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27040576 | ||||||
| chr9:27040936
|
T | C | 1 | a0002c0002t0002g0086 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1055-3806T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27040936 | ||||||
| chr9:27041068
|
CCA | C | 4 | a0001c0001t0001g0153a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 4 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1055-3673_1055-367 others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041068 | ||||||
| chr9:27041070
|
A | G | 1 | a0007c0007t0019g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1055-3672A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041070 | ||||||
| chr9:27041092
|
C | T | 2 | a0002c0002t0002g0041a0003c0003t0002g0097 | 2 | NA19080.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1055-3650C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041092 | ||||||
| chr9:27041174
|
A | G | 1 | a0002c0002t0002g0060 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1055-3568A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041174 | ||||||
| chr9:27041317
|
C | T | 130 | a0001c0001t0002g0183a0001c0001t0009g0030a0001c0001t0009g0031others(127): Show | 130 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.1055-3425C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041317 | ||||||
| chr9:27041334
|
A | G | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055-3408A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041334 | ||||||
| chr9:27041340
|
A | G | 1 | a0003c0003t0022g0054 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1055-3402A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041340 | ||||||
| chr9:27041355
|
A | C | 1 | a0001c0001t0001g0244 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1055-3387A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041355 | ||||||
| chr9:27041393
|
A | G | 92 | a0001c0001t0002g0183a0001c0001t0009g0030a0001c0001t0009g0031others(89): Show | 92 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1055-3349A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041393 | ||||||
| chr9:27041501
|
C | T | 86 | a0001c0001t0002g0183a0001c0001t0018g0127a0002c0002t0002g0006others(83): Show | 86 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1055-3241C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041501 | ||||||
| chr9:27041518
|
G | A | 1 | a0003c0003t0002g0126 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1055-3224G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041518 | ||||||
| chr9:27041556
|
G | A | 2 | a0001c0001t0018g0127a0011c0010t0017g0114 | 2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1055-3186G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041556 | ||||||
| chr9:27041663
|
G | A | 28 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(25): Show | 28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1055-3079G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041663 | ||||||
| chr9:27041678
|
C | T | 159 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0115others(156): Show | 159 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.1055-3064C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041678 | ||||||
| chr9:27041834
|
T | A | 12 | a0006c0006t0001g0325a0006c0006t0001g0326a0006c0006t0001g0327others(9): Show | 12 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1055-2908T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041834 | ||||||
| chr9:27041835
|
C | T | 2 | a0006c0006t0001g0326a0006c0006t0001g0327 | 2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1055-2907C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27041835 | ||||||
| chr9:27042163
|
C | T | 3 | a0001c0001t0010g0033a0001c0001t0010g0034a0001c0001t0011g0035 | 3 | HG01884.hp1 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1055-2579C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27042163 | ||||||
| chr9:27042271
|
A | G | 1 | a0001c0001t0002g0183 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1055-2471A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27042271 | ||||||
| chr9:27042359
|
T | C | 3 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0019g0118 | 3 | HG01255.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1055-2383T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27042359 | ||||||
| chr9:27042398
|
G | A | 14 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(11): Show | 14 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1055-2344G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27042398 | ||||||
| chr9:27042533
|
A | G | 2 | a0001c0001t0011g0032a0001c0001t0011g0035 | 2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1055-2209A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27042533 | ||||||
| chr9:27042863
|
A | G | 2 | a0002c0002t0002g0077a0002c0002t0002g0079 | 2 | NA18980.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1055-1879A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27042863 | ||||||
| chr9:27042983
|
G | A | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1055-1759G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27042983 | ||||||
| chr9:27043002
|
C | A | 1 | a0001c0012t0003g0302 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1055-1740C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27043002 | ||||||
| chr9:27043130
|
G | A | 10 | a0001c0001t0001g0152a0001c0001t0001g0176a0001c0001t0001g0179others(7): Show | 10 | HG00597.hp2 HG02129.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1055-1612G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27043130 | ||||||
| chr9:27043644
|
A | G | 2 | a0006c0006t0001g0326a0006c0006t0001g0327 | 2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1055-1098A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27043644 | ||||||
| chr9:27043916
|
CTTCTCT | C | 4 | a0001c0001t0018g0127a0001c0001t0033g0104a0007c0007t0023g0005others(1): Show | 4 | HG02886.hp2 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1055-823_1055-818d others(8): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 27043916 | |||||
| chr9:27043925
|
T | A | 4 | a0001c0001t0018g0127a0001c0001t0033g0104a0007c0007t0023g0005others(1): Show | 4 | HG02886.hp2 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1055-817T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27043925 | ||||||
| chr9:27044327
|
A | G | 3 | a0001c0001t0001g0337a0001c0001t0001g0338a0001c0001t0001g0339 | 3 | HG02630.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1055-415A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27044327 | ||||||
| chr9:27044493
|
A | T | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1055-249A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27044493 | ||||||
| chr9:27044566
|
A | T | 32 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0137others(29): Show | 32 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.1055-176A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27044566 | ||||||
| chr9:27044589
|
G | A | 16 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0151others(13): Show | 16 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.1055-153G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27044589 | ||||||
| chr9:27044645
|
T | C | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1055-97T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 13/19 | chr9 | 27044645 | ||||||
| chr9:27045079
|
A | G | 1 | a0007c0007t0019g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1108+284A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045079 | ||||||
| chr9:27045219
|
G | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG03490.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1108+424G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045219 | ||||||
| chr9:27045260
|
C | A | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1108+465C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045260 | ||||||
| chr9:27045330
|
A | G | 1 | a0007c0007t0019g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1108+535A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045330 | ||||||
| chr9:27045344
|
T | C | 1 | a0002c0002t0002g0093 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1108+549T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045344 | ||||||
| chr9:27045389
|
A | G | 1 | a0006c0006t0026g0206 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1108+594A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045389 | ||||||
| chr9:27045639
|
T | A | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1108+844T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045639 | ||||||
| chr9:27045745
|
A | G | 15 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(12): Show | 15 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1108+950A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045745 | ||||||
| chr9:27045769
|
A | T | 135 | a0001c0001t0002g0183a0001c0001t0002g0289a0001c0001t0009g0030others(132): Show | 135 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.1108+974A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045769 | ||||||
| chr9:27045872
|
T | C | 1 | a0002c0002t0002g0063 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1108+1077T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045872 | ||||||
| chr9:27045985
|
C | G | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1108+1190C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27045985 | ||||||
| chr9:27046279
|
G | C | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1109-995G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27046279 | ||||||
| chr9:27046289
|
A | G | 5 | a0003c0003t0006g0112a0003c0003t0006g0113a0007c0007t0006g0016others(2): Show | 5 | HG00733.hp1 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1109-985A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27046289 | ||||||
| chr9:27046343
|
G | A | 134 | a0001c0001t0002g0183a0001c0001t0009g0030a0001c0001t0009g0031others(131): Show | 134 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.1109-931G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27046343 | ||||||
| chr9:27046443
|
A | G | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1109-831A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27046443 | ||||||
| chr9:27046470
|
C | T | 28 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(25): Show | 28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1109-804C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27046470 | ||||||
| chr9:27046643
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1109-631A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27046643 | ||||||
| chr9:27046904
|
G | A | 2 | a0003c0003t0002g0042a0003c0003t0002g0049 | 2 | HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1109-370G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27046904 | ||||||
| chr9:27046945
|
C | T | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1109-329C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27046945 | ||||||
| chr9:27047008
|
G | A | 134 | a0001c0001t0002g0183a0001c0001t0009g0030a0001c0001t0009g0031others(131): Show | 134 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.1109-266G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27047008 | ||||||
| chr9:27047077
|
G | C | 1 | a0001c0001t0003g0298 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1109-197G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27047077 | ||||||
| chr9:27047120
|
C | T | 2 | a0001c0001t0003g0299a0001c0001t0003g0300 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1109-154C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27047120 | ||||||
| chr9:27047123
|
G | C | 1 | a0003c0003t0002g0097 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1109-151G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27047123 | ||||||
| chr9:27047160
|
G | A | 4 | a0002c0002t0002g0050a0002c0002t0002g0053a0002c0002t0002g0066others(1): Show | 4 | HG00735.hp2 HG01099.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.1109-114G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27047160 | ||||||
| chr9:27047194
|
A | T | 12 | a0006c0006t0001g0325a0006c0006t0001g0326a0006c0006t0001g0327others(9): Show | 12 | HG01069.hp2 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1109-80A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27047194 | ||||||
| chr9:27047243
|
A | T | 28 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(25): Show | 28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1109-31A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27047243 | ||||||
| chr9:27047248
|
T | C | 270 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(267): Show | 270 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.1109-26T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 14/19 | chr9 | 27047248 | ||||||
| chr9:27047462
|
T | C | 28 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0208others(25): Show | 28 | HG00609.hp2 HG00741.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1206+91T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 15/19 | chr9 | 27047462 | ||||||
| chr9:27047633
|
AATT | A | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1206+268_1206+270d others(5): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr9 | 27047633 | |||||
| chr9:27047663
|
T | C | 1 | a0007c0007t0019g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1206+292T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 15/19 | chr9 | 27047663 | ||||||
| chr9:27047784
|
G | A | 4 | a0005c0004t0004g0013a0005c0004t0004g0015a0005c0004t0004g0021others(1): Show | 4 | NA18960.hp2 NA18973.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207-364G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 15/19 | chr9 | 27047784 | ||||||
| chr9:27047844
|
C | T | 4 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0019g0118others(1): Show | 4 | HG01255.hp2 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207-304C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 15/19 | chr9 | 27047844 | ||||||
| chr9:27047940
|
A | C | 1 | a0002c0002t0002g0050 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1207-208A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 15/19 | chr9 | 27047940 | ||||||
| chr9:27048313
|
A | T | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0115others(7): Show | 10 | HG01192.hp1 HG01255.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1333+39A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048313 | ||||||
| chr9:27048324
|
A | G | 5 | a0001c0001t0001g0107a0007c0007t0008g0003a0007c0007t0008g0004others(2): Show | 5 | HG01255.hp2 HG02615.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1333+50A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048324 | ||||||
| chr9:27048443
|
T | C | 1 | a0002c0002t0002g0080 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1333+169T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048443 | ||||||
| chr9:27048533
|
T | A | 135 | a0001c0001t0001g0107a0001c0001t0002g0183a0001c0001t0002g0289others(132): Show | 135 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.1333+259T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048533 | ||||||
| chr9:27048698
|
A | G | 4 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0019g0118others(1): Show | 4 | HG01255.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333+424A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048698 | ||||||
| chr9:27048736
|
G | C | 1 | a0001c0001t0033g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1333+462G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048736 | ||||||
| chr9:27048755
|
T | G | 1 | a0001c0001t0001g0219 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1333+481T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048755 | ||||||
| chr9:27048808
|
C | T | 2 | a0003c0003t0002g0110a0003c0003t0002g0111 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1333+534C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048808 | ||||||
| chr9:27048896
|
C | A | 1 | a0001c0001t0028g0301 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1333+622C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048896 | ||||||
| chr9:27048917
|
T | C | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1333+643T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048917 | ||||||
| chr9:27048963
|
C | T | 1 | a0001c0001t0001g0337 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1333+689C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27048963 | ||||||
| chr9:27049027
|
G | T | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1333+753G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049027 | ||||||
| chr9:27049054
|
A | G | 1 | a0002c0002t0002g0040 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1333+780A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049054 | ||||||
| chr9:27049111
|
G | T | 1 | a0007c0007t0019g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1333+837G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049111 | ||||||
| chr9:27049137
|
T | C | 14 | a0005c0004t0004g0013a0005c0004t0004g0014a0005c0004t0004g0015others(11): Show | 14 | HG00323.hp2 HG00733.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1333+863T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049137 | ||||||
| chr9:27049272
|
G | A | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1333+998G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049272 | ||||||
| chr9:27049306
|
A | G | 4 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333+1032A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049306 | ||||||
| chr9:27049377
|
C | A | 1 | a0005c0004t0004g0024 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1333+1103C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049377 | ||||||
| chr9:27049385
|
C | T | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333+1111C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049385 | ||||||
| chr9:27049658
|
A | G | 88 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0250others(85): Show | 88 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1333+1384A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049658 | ||||||
| chr9:27049661
|
T | G | 4 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333+1387T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049661 | ||||||
| chr9:27049835
|
C | A | 1 | a0001c0001t0001g0184 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1333+1561C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049835 | ||||||
| chr9:27049864
|
G | A | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1333+1590G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049864 | ||||||
| chr9:27049940
|
A | G | 14 | a0001c0001t0002g0289a0002c0002t0002g0047a0002c0002t0002g0048others(11): Show | 14 | HG00639.hp1 HG01081.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1333+1666A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049940 | ||||||
| chr9:27049966
|
A | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0035g0242 | 3 | HG01099.hp2 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1333+1692A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049966 | ||||||
| chr9:27049979
|
A | G | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1333+1705A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049979 | ||||||
| chr9:27049989
|
T | A | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333+1715T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049989 | ||||||
| chr9:27049990
|
A | G | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333+1716A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27049990 | ||||||
| chr9:27050009
|
G | C | 1 | a0001c0001t0033g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1333+1735G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27050009 | ||||||
| chr9:27050025
|
G | A | 30 | a0001c0001t0009g0030a0001c0001t0009g0031a0004c0005t0005g0308others(27): Show | 30 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1333+1751G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27050025 | ||||||
| chr9:27050046
|
C | CTTAT | 9 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(6): Show | 9 | HG01069.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1333+1797_1333+180 others(8): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27050046 | |||||
| chr9:27050118
|
C | T | 1 | a0002c0002t0002g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1333+1844C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27050118 | ||||||
| chr9:27050161
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1333+1887G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27050161 | ||||||
| chr9:27050595
|
C | A | 33 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0137others(30): Show | 33 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.1333+2321C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27050595 | ||||||
| chr9:27050758
|
A | G | 14 | a0001c0001t0001g0225a0001c0001t0001g0227a0001c0001t0001g0231others(11): Show | 14 | HG01074.hp2 HG01243.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1333+2484A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27050758 | ||||||
| chr9:27050768
|
G | T | 14 | a0001c0001t0001g0225a0001c0001t0001g0227a0001c0001t0001g0231others(11): Show | 14 | HG01074.hp2 HG01243.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1333+2494G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27050768 | ||||||
| chr9:27050781
|
T | C | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1333+2507T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27050781 | ||||||
| chr9:27050863
|
A | T | 92 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0250others(89): Show | 92 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1333+2589A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27050863 | ||||||
| chr9:27050874
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1333+2600T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27050874 | ||||||
| chr9:27051001
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1333+2727G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27051001 | ||||||
| chr9:27051043
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1333+2769T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27051043 | ||||||
| chr9:27051070
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1333+2796G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27051070 | ||||||
| chr9:27051192
|
A | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG03490.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1333+2918A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27051192 | ||||||
| chr9:27051215
|
G | A | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1333+2941G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27051215 | ||||||
| chr9:27051428
|
T | TA | 4 | a0003c0003t0002g0067a0003c0003t0002g0100a0003c0003t0021g0099others(1): Show | 4 | HG02300.hp1 NA18964.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333+3161dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27051428 | |||||
| chr9:27051524
|
A | G | 3 | a0001c0001t0001g0287a0001c0001t0001g0290a0001c0001t0001g0304 | 3 | HG02257.hp2 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1333+3250A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27051524 | ||||||
| chr9:27051814
|
G | A | 139 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0250others(136): Show | 139 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.1333+3540G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27051814 | ||||||
| chr9:27051876
|
G | A | 5 | a0001c0001t0001g0102a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG01192.hp1 HG02280.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1333+3602G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27051876 | ||||||
| chr9:27051893
|
G | C | 6 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0008g0003others(3): Show | 6 | HG02615.hp1 HG03041.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1333+3619G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27051893 | ||||||
| chr9:27052179
|
G | A | 2 | a0001c0001t0018g0127a0011c0010t0017g0114 | 2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1334-3430G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27052179 | ||||||
| chr9:27052307
|
C | G | 2 | a0001c0001t0013g0265a0001c0001t0013g0266 | 2 | NA18959.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1334-3302C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27052307 | ||||||
| chr9:27052327
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1334-3282T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27052327 | ||||||
| chr9:27052423
|
A | C | 1 | a0001c0001t0032g0224 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1334-3186A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27052423 | ||||||
| chr9:27052468
|
A | G | 2 | a0003c0003t0002g0110a0003c0003t0002g0111 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1334-3141A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27052468 | ||||||
| chr9:27052489
|
C | T | 1 | a0004c0005t0005g0319 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1334-3120C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27052489 | ||||||
| chr9:27052507
|
C | CA | 25 | a0001c0001t0001g0106a0001c0001t0001g0179a0001c0001t0001g0182others(22): Show | 25 | HG00733.hp1 HG01361.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1334-3079dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27052507 | |||||
| chr9:27052507
|
CA | C | 31 | a0001c0001t0001g0156a0001c0001t0001g0220a0001c0001t0001g0237others(28): Show | 31 | HG00639.hp2 HG01069.hp2 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.1334-3079delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27052507 | |||||
| chr9:27052508
|
A | C | 6 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(3): Show | 6 | NA18944.hp2 NA18966.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1334-3101A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27052508 | ||||||
| chr9:27052605
|
C | G | 2 | a0001c0001t0018g0127a0011c0010t0017g0114 | 2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1334-3004C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27052605 | ||||||
| chr9:27052856
|
A | ATGT | 4 | a0001c0001t0010g0033a0001c0001t0010g0034a0001c0001t0011g0035others(1): Show | 4 | HG01884.hp1 HG02080.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1334-2730_1334-272 others(7): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27052856 | |||||
| chr9:27052856
|
ATGT | A | 3 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0023g0005 | 3 | HG03041.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1334-2730_1334-272 others(7): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27052856 | |||||
| chr9:27052930
|
T | C | 4 | a0001c0001t0001g0149a0001c0001t0001g0195a0001c0001t0001g0197others(1): Show | 4 | HG01074.hp1 HG01175.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1334-2679T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27052930 | ||||||
| chr9:27053024
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1334-2585C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053024 | ||||||
| chr9:27053124
|
A | G | 2 | a0003c0003t0002g0090a0003c0003t0002g0092 | 2 | NA18975.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1334-2485A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053124 | ||||||
| chr9:27053147
|
G | GC | 340 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(337): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1334-2461dupC | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27053147 | |||||
| chr9:27053161
|
C | CT | 24 | a0001c0001t0001g0147a0001c0001t0001g0184a0001c0001t0001g0190others(21): Show | 24 | HG00609.hp2 HG00639.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.1334-2422dupT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27053161 | |||||
| chr9:27053161
|
CT | C | 188 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0106others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1334-2422delT | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27053161 | |||||
| chr9:27053161
|
CTT | C | 32 | a0001c0001t0001g0115a0001c0001t0001g0137a0002c0002t0002g0006others(29): Show | 32 | HG00323.hp2 HG00733.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.1334-2423_1334-242 others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27053161 | |||||
| chr9:27053227
|
T | TTATA | 3 | a0001c0001t0010g0033a0001c0001t0010g0034a0001c0001t0011g0035 | 3 | HG01884.hp1 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1334-2380_1334-237 others(8): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27053227 | |||||
| chr9:27053263
|
C | T | 1 | a0003c0003t0002g0097 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1334-2346C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053263 | ||||||
| chr9:27053280
|
A | T | 2 | a0001c0001t0018g0127a0011c0010t0017g0114 | 2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1334-2329A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053280 | ||||||
| chr9:27053429
|
T | G | 95 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0250others(92): Show | 95 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.1334-2180T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053429 | ||||||
| chr9:27053481
|
G | T | 2 | a0001c0001t0018g0127a0011c0010t0017g0114 | 2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1334-2128G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053481 | ||||||
| chr9:27053652
|
C | G | 132 | a0001c0001t0002g0183a0001c0001t0009g0030a0001c0001t0009g0031others(129): Show | 132 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.1334-1957C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053652 | ||||||
| chr9:27053783
|
T | A | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1334-1826T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053783 | ||||||
| chr9:27053824
|
G | A | 1 | a0001c0001t0014g0001 | 2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1334-1785G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053824 | ||||||
| chr9:27053897
|
T | C | 1 | a0004c0005t0005g0317 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1334-1712T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053897 | ||||||
| chr9:27053979
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1334-1630A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053979 | ||||||
| chr9:27053990
|
C | T | 332 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(329): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1334-1619C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27053990 | ||||||
| chr9:27054116
|
G | C | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1334-1493G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27054116 | ||||||
| chr9:27054157
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG01192.hp1 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1334-1452G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27054157 | ||||||
| chr9:27054299
|
C | T | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1334-1310C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27054299 | ||||||
| chr9:27054344
|
A | G | 1 | a0004c0005t0005g0317 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1334-1265A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27054344 | ||||||
| chr9:27054668
|
G | A | 3 | a0001c0001t0003g0272a0001c0001t0003g0273a0001c0001t0003g0274 | 3 | HG01069.hp1 HG03654.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1334-941G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27054668 | ||||||
| chr9:27054697
|
A | G | 1 | a0001c0001t0003g0281 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1334-912A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27054697 | ||||||
| chr9:27054791
|
T | G | 1 | a0001c0001t0003g0288 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1334-818T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27054791 | ||||||
| chr9:27054854
|
T | G | 2 | a0001c0001t0002g0289a0001c0001t0016g0292 | 2 | HG02273.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1334-755T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27054854 | ||||||
| chr9:27054929
|
A | T | 3 | a0005c0004t0004g0013a0005c0004t0004g0015a0005c0004t0004g0027 | 3 | NA18960.hp2 NA18973.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1334-680A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27054929 | ||||||
| chr9:27054959
|
T | C | 28 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0310others(25): Show | 28 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1334-650T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27054959 | ||||||
| chr9:27055013
|
G | A | 1 | a0011c0010t0017g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1334-596G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27055013 | ||||||
| chr9:27055085
|
G | C | 3 | a0001c0001t0010g0033a0001c0001t0010g0034a0001c0001t0011g0035 | 3 | HG01884.hp1 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1334-524G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27055085 | ||||||
| chr9:27055218
|
T | G | 1 | a0002c0002t0002g0050 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1334-391T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27055218 | ||||||
| chr9:27055226
|
A | AAT | 7 | a0001c0001t0010g0033a0001c0001t0010g0034a0001c0001t0011g0035others(4): Show | 7 | HG01255.hp2 HG01884.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1334-373_1334-372d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 27055226 | |||||
| chr9:27055267
|
T | C | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1334-342T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27055267 | ||||||
| chr9:27055285
|
G | A | 127 | a0001c0001t0002g0183a0001c0001t0009g0030a0001c0001t0009g0031others(124): Show | 127 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.1334-324G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27055285 | ||||||
| chr9:27055316
|
T | C | 1 | a0011c0010t0017g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1334-293T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27055316 | ||||||
| chr9:27055512
|
T | A | 1 | a0001c0001t0001g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1334-97T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27055512 | ||||||
| chr9:27055540
|
G | A | 1 | a0002c0002t0002g0093 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1334-69G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27055540 | ||||||
| chr9:27055549
|
T | A | 1 | a0001c0001t0011g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1334-60T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27055549 | ||||||
| chr9:27055568
|
A | T | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0115others(7): Show | 10 | HG01192.hp1 HG01255.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1334-41A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 16/19 | chr9 | 27055568 | ||||||
| chr9:27055844
|
T | C | 2 | a0001c0001t0028g0301a0010c0013t0031g0284 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1497+72T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 17/19 | chr9 | 27055844 | ||||||
| chr9:27056147
|
G | GTTA | 5 | a0003c0003t0006g0112a0003c0003t0006g0113a0007c0007t0006g0016others(2): Show | 5 | HG00733.hp1 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498-183_1498-181d others(5): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr9 | 27056147 | |||||
| chr9:27056213
|
A | T | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1498-121A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 17/19 | chr9 | 27056213 | ||||||
| chr9:27056523
|
A | T | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1623+64A>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27056523 | ||||||
| chr9:27056731
|
A | G | 1 | a0001c0001t0035g0242 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1623+272A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27056731 | ||||||
| chr9:27056789
|
T | C | 1 | a0011c0010t0017g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1623+330T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27056789 | ||||||
| chr9:27056858
|
G | GGATA | 53 | a0001c0001t0001g0105a0001c0001t0001g0141a0001c0001t0001g0142others(50): Show | 53 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.1623+444_1623+447d others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr9 | 27056858 | |||||
| chr9:27056858
|
G | GGATAGAT others(1): Show |
9 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0161others(6): Show | 9 | HG00099.hp2 HG00738.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.1623+440_1623+447d others(10): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr9 | 27056858 | |||||
| chr9:27056858
|
G | GGATAGAT others(5): Show |
2 | a0001c0001t0001g0179a0002c0002t0002g0050 | 2 | NA18944.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1623+436_1623+447d others(14): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr9 | 27056858 | |||||
| chr9:27056858
|
GGATA | G | 85 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0107others(82): Show | 85 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.1623+444_1623+447d others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr9 | 27056858 | |||||
| chr9:27056858
|
GGATAGAT others(1): Show |
G | 36 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0143others(33): Show | 36 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.1623+440_1623+447d others(10): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr9 | 27056858 | |||||
| chr9:27056858
|
GGATAGAT others(5): Show |
G | 5 | a0001c0001t0001g0262a0001c0001t0009g0030a0001c0001t0009g0031others(2): Show | 5 | HG01099.hp1 HG01496.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1623+436_1623+447d others(14): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr9 | 27056858 | |||||
| chr9:27056858
|
GGATAGAT others(9): Show |
G | 1 | a0004c0005t0005g0313 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1623+432_1623+447d others(18): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr9 | 27056858 | |||||
| chr9:27056958
|
A | G | 1 | a0005c0004t0004g0020 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1623+499A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27056958 | ||||||
| chr9:27057247
|
C | A | 1 | a0008c0009t0008g0002 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1623+788C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27057247 | ||||||
| chr9:27057255
|
T | G | 1 | a0001c0001t0001g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1623+796T>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27057255 | ||||||
| chr9:27057457
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1623+998T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27057457 | ||||||
| chr9:27057543
|
A | G | 1 | a0002c0002t0002g0093 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1623+1084A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27057543 | ||||||
| chr9:27057645
|
C | G | 1 | a0002c0002t0002g0043 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1623+1186C>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27057645 | ||||||
| chr9:27057719
|
G | A | 116 | a0001c0001t0002g0183a0002c0002t0002g0006a0002c0002t0002g0007others(113): Show | 116 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.1623+1260G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27057719 | ||||||
| chr9:27057743
|
A | C | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1623+1284A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27057743 | ||||||
| chr9:27057750
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1623+1291C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27057750 | ||||||
| chr9:27058108
|
A | G | 1 | a0001c0001t0001g0244 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1623+1649A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058108 | ||||||
| chr9:27058123
|
G | C | 307 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(304): Show | 307 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1623+1664G>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058123 | ||||||
| chr9:27058203
|
C | A | 1 | a0001c0001t0001g0228 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1623+1744C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058203 | ||||||
| chr9:27058273
|
G | T | 1 | a0001c0001t0001g0163 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1623+1814G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058273 | ||||||
| chr9:27058374
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1623+1915C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058374 | ||||||
| chr9:27058459
|
T | C | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1623+2000T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058459 | ||||||
| chr9:27058562
|
G | A | 134 | a0001c0001t0002g0183a0001c0001t0002g0289a0001c0001t0009g0030others(131): Show | 134 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.1624-2029G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058562 | ||||||
| chr9:27058580
|
G | A | 1 | a0004c0005t0005g0313 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1624-2011G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058580 | ||||||
| chr9:27058603
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1624-1988G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058603 | ||||||
| chr9:27058638
|
T | A | 5 | a0003c0003t0006g0112a0003c0003t0006g0113a0007c0007t0006g0016others(2): Show | 5 | HG00733.hp1 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1624-1953T>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058638 | ||||||
| chr9:27058920
|
T | C | 9 | a0001c0001t0001g0152a0001c0001t0001g0176a0001c0001t0001g0179others(6): Show | 9 | HG00597.hp2 HG02129.hp1 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.1624-1671T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058920 | ||||||
| chr9:27058975
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1624-1616C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27058975 | ||||||
| chr9:27059207
|
T | C | 4 | a0001c0001t0010g0033a0001c0001t0010g0034a0001c0001t0011g0032others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1624-1384T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27059207 | ||||||
| chr9:27059612
|
A | G | 1 | a0002c0002t0002g0086 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1624-979A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27059612 | ||||||
| chr9:27059621
|
CTG | C | 10 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0263others(7): Show | 10 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.1624-969_1624-968d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27059621 | ||||||
| chr9:27059633
|
G | A | 1 | a0009c0011t0001g0235 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1624-958G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27059633 | ||||||
| chr9:27059801
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1624-790C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27059801 | ||||||
| chr9:27059945
|
A | G | 2 | a0004c0005t0005g0308a0004c0005t0005g0309 | 2 | HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1624-646A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27059945 | ||||||
| chr9:27060070
|
G | T | 4 | a0001c0001t0010g0033a0001c0001t0010g0034a0001c0001t0011g0032others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1624-521G>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27060070 | ||||||
| chr9:27060212
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1624-379T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27060212 | ||||||
| chr9:27060323
|
T | C | 2 | a0003c0003t0006g0112a0003c0003t0006g0113 | 2 | HG02055.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1624-268T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27060323 | ||||||
| chr9:27060346
|
G | A | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1624-245G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27060346 | ||||||
| chr9:27060436
|
TTTAA | T | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1624-153_1624-150d others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr9 | 27060436 | |||||
| chr9:27060457
|
G | A | 6 | a0001c0001t0009g0030a0001c0001t0009g0031a0007c0007t0008g0003others(3): Show | 6 | HG02615.hp1 HG03041.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1624-134G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 18/19 | chr9 | 27060457 | ||||||
| chr9:27060686
|
C | T | 1 | a0002c0002t0002g0101 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1684+35C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060686 | ||||||
| chr9:27060701
|
A | G | 2 | a0003c0003t0002g0322a0003c0003t0002g0323 | 2 | HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1684+50A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060701 | ||||||
| chr9:27060736
|
G | A | 4 | a0007c0007t0008g0003a0007c0007t0008g0004a0007c0007t0023g0005others(1): Show | 4 | HG02615.hp1 HG03209.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1684+85G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060736 | ||||||
| chr9:27060737
|
C | A | 1 | a0001c0001t0001g0141 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1684+86C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060737 | ||||||
| chr9:27060814
|
T | C | 1 | a0001c0001t0033g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1684+163T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060814 | ||||||
| chr9:27060823
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1684+172G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060823 | ||||||
| chr9:27060848
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1684+197C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060848 | ||||||
| chr9:27060884
|
A | C | 5 | a0001c0001t0001g0107a0007c0007t0008g0003a0007c0007t0008g0004others(2): Show | 5 | HG02615.hp1 HG03209.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1684+233A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060884 | ||||||
| chr9:27060927
|
A | C | 1 | a0001c0001t0003g0297 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1684+276A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060927 | ||||||
| chr9:27060940
|
C | T | 1 | a0002c0002t0002g0062 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1684+289C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060940 | ||||||
| chr9:27060961
|
C | CA | 54 | a0001c0001t0001g0145a0001c0001t0001g0148a0001c0001t0001g0160others(51): Show | 54 | HG00621.hp2 HG00639.hp2 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.1684+340dupA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27060961 | |||||
| chr9:27060961
|
CA | C | 99 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0106others(96): Show | 99 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1684+340delA | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27060961 | |||||
| chr9:27060961
|
CAA | C | 8 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0116others(5): Show | 8 | HG01255.hp2 HG02273.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1684+339_1684+340d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27060961 | |||||
| chr9:27060961
|
CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0001g0287a0001c0001t0001g0290a0001c0001t0001g0304 | 3 | HG02257.hp2 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1684+328_1684+340d others(15): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27060961 | |||||
| chr9:27060961
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0221 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1684+326_1684+340d others(17): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27060961 | |||||
| chr9:27060961
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0222 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1684+325_1684+340d others(18): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27060961 | |||||
| chr9:27060980
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1684+329A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060980 | ||||||
| chr9:27060990
|
A | G | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1684+339A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27060990 | ||||||
| chr9:27061144
|
G | GGT | 6 | a0004c0005t0005g0308a0004c0005t0005g0309a0004c0005t0005g0311others(3): Show | 6 | HG01256.hp1 HG02735.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1684+517_1684+518d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061144 | |||||
| chr9:27061144
|
GGT | G | 152 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0001g0106others(149): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1684+517_1684+518d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061144 | |||||
| chr9:27061144
|
GGTGT | G | 98 | a0001c0001t0001g0102a0001c0001t0002g0183a0001c0001t0009g0030others(95): Show | 98 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1684+515_1684+518d others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061144 | |||||
| chr9:27061168
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1684+517T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061168 | ||||||
| chr9:27061170
|
C | T | 1 | a0007c0007t0023g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1684+519C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061170 | ||||||
| chr9:27061174
|
C | T | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1684+523C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061174 | ||||||
| chr9:27061335
|
A | G | 1 | a0001c0001t0018g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1684+684A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061335 | ||||||
| chr9:27061342
|
C | A | 2 | a0001c0001t0011g0032a0001c0001t0011g0035 | 2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1684+691C>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061342 | ||||||
| chr9:27061385
|
C | T | 83 | a0001c0001t0002g0183a0002c0002t0002g0006a0002c0002t0002g0007others(80): Show | 83 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.1684+734C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061385 | ||||||
| chr9:27061386
|
G | A | 4 | a0001c0001t0010g0033a0001c0001t0010g0034a0001c0001t0011g0032others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1684+735G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061386 | ||||||
| chr9:27061394
|
A | C | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1684+743A>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061394 | ||||||
| chr9:27061562
|
A | G | 1 | a0001c0001t0010g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1684+911A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061562 | ||||||
| chr9:27061677
|
G | GTA | 44 | a0001c0001t0001g0105a0001c0001t0001g0132a0001c0001t0001g0133others(41): Show | 44 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.1685-923_1685-922d others(4): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061677 | |||||
| chr9:27061677
|
G | GTATA | 15 | a0001c0001t0001g0156a0001c0001t0001g0160a0001c0001t0011g0035others(12): Show | 15 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1685-925_1685-922d others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061677 | |||||
| chr9:27061677
|
G | GTATATA | 24 | a0001c0001t0011g0032a0003c0003t0006g0112a0003c0003t0006g0113others(21): Show | 24 | HG00733.hp1 HG00733.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1685-927_1685-922d others(8): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061677 | |||||
| chr9:27061677
|
G | GTATATAT others(1): Show |
6 | a0002c0002t0002g0039a0002c0002t0002g0044a0002c0002t0002g0045others(3): Show | 6 | HG00597.hp1 HG03491.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.1685-929_1685-922d others(10): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061677 | |||||
| chr9:27061677
|
G | GTATATAT others(3): Show |
54 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0008others(51): Show | 54 | HG00408.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1685-931_1685-922d others(12): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061677 | |||||
| chr9:27061677
|
G | GTATATAT others(5): Show |
18 | a0002c0002t0002g0046a0002c0002t0002g0047a0002c0002t0002g0059others(15): Show | 18 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.1685-933_1685-922d others(14): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061677 | |||||
| chr9:27061677
|
G | GTATATAT others(7): Show |
2 | a0002c0002t0002g0056a0002c0002t0002g0057 | 2 | HG01928.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1685-935_1685-922d others(16): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061677 | |||||
| chr9:27061677
|
G | GTATATAT others(9): Show |
4 | a0001c0001t0002g0183a0001c0001t0018g0127a0002c0002t0002g0058others(1): Show | 4 | HG00621.hp2 HG03540.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1685-937_1685-922d others(18): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061677 | |||||
| chr9:27061677
|
G | GTATATAT others(11): Show |
1 | a0002c0002t0002g0051 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1685-939_1685-922d others(20): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061677 | |||||
| chr9:27061677
|
G | GTGTATAT others(3): Show |
1 | a0002c0002t0002g0075 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1685-940_1685-939i others(12): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 27061677 | |||||
| chr9:27061680
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1685-938T>C | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061680 | ||||||
| chr9:27061697
|
G | A | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1685-921G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061697 | ||||||
| chr9:27061700
|
C | T | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1685-918C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061700 | ||||||
| chr9:27061707
|
T | TGTAC | 4 | a0003c0003t0002g0321a0003c0003t0002g0322a0003c0003t0002g0323others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1685-911_1685-910i others(6): Show |
IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061707 | ||||||
| chr9:27061742
|
A | G | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1685-876A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061742 | ||||||
| chr9:27061904
|
G | A | 1 | a0004c0005t0005g0310 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1685-714G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27061904 | ||||||
| chr9:27062344
|
A | G | 3 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121 | 3 | HG03041.hp1 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1685-274A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27062344 | ||||||
| chr9:27062427
|
G | A | 4 | a0007c0007t0008g0003a0007c0007t0008g0004a0007c0007t0023g0005others(1): Show | 4 | HG02615.hp1 HG03209.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1685-191G>A | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27062427 | ||||||
| chr9:27062478
|
A | G | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG01496.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1685-140A>G | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27062478 | ||||||
| chr9:27062486
|
C | T | 3 | a0007c0007t0008g0003a0007c0007t0008g0004a0008c0009t0008g0002 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1685-132C>T | IFT74 | ENSG00000096872.17 | transcript | ENST00000380062.10 | protein_coding | 19/19 | chr9 | 27062486 |