| geneid | 54103 |
|---|---|
| ensemblid | ENSG00000186088.16 |
| hgncid | 28042 |
| symbol | GSAP |
| name | gamma-secretase activating protein |
| refseq_nuc | NM_017439.4 |
| refseq_prot | NP_059135.2 |
| ensembl_nuc | ENST00000257626.12 |
| ensembl_prot | ENSP00000257626.7 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 77310751 |
| end | 77416349 |
| strand | - |
| ver | v1.2 |
| region | chr7:77310751-77416349 |
| region5000 | chr7:77305751-77421349 |
| regionname0 | GSAP_chr7_77310751_77416349 |
| regionname5000 | GSAP_chr7_77305751_77421349 |
| 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 | 0/1 | 854 | 208 | 35 | 45 | 110 | 6 | 11 | 81 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0002 | 0/0 | 854 | 63 | 15 | 5 | 25 | 4 | 14 | 24 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0003 | 0/0 | 854 | 27 | 14 | 4 | 4 | 3 | 2 | 3 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0004 | 0/0 | 854 | 20 | 2 | 2 | 13 | 0 | 3 | 10 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0005 | 1/0 | 854 | 11 | 0 | 3 | 0 | 5 | 2 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0006 | 0/0 | 854 | 9 | 6 | 2 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0007 | 0/0 | 854 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0008 | 0/0 | 854 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0009 | 0/0 | 854 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0010 | 0/0 | 854 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0011 | 0/0 | 854 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0012 | 0/0 | 854 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0013 | 0/0 | 854 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0014 | 0/0 | 854 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2565 | 107 | 6 | 25 | 62 | 6 | 7 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0002 | 0/0 | 2565 | 90 | 20 | 19 | 48 | 0 | 3 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0003 | 0/0 | 2565 | 50 | 14 | 4 | 15 | 4 | 13 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0004 | 0/0 | 2565 | 21 | 11 | 4 | 1 | 3 | 2 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0005 | 0/0 | 2565 | 19 | 2 | 2 | 12 | 0 | 3 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0006 | 1/0 | 2565 | 11 | 0 | 3 | 0 | 5 | 2 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0007 | 0/0 | 2565 | 10 | 0 | 0 | 10 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0008 | 0/0 | 2565 | 8 | 6 | 2 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0009 | 0/0 | 2565 | 6 | 3 | 0 | 3 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0010 | 0/0 | 2565 | 6 | 6 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0011 | 0/0 | 2565 | 5 | 5 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0012 | 0/0 | 2565 | 2 | 0 | 2 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0013 | 0/0 | 2565 | 2 | 2 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0014 | 0/0 | 2565 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0015 | 0/0 | 2565 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0016 | 0/0 | 2565 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0017 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0018 | 0/0 | 2565 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0019 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0020 | 0/0 | 2565 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0021 | 0/0 | 2565 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0022 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0023 | 0/0 | 2565 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0024 | 0/0 | 2565 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0025 | 0/0 | 2565 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0026 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0027 | 0/0 | 2565 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| c0028 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| 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 | 636 | 280 | 40 | 54 | 140 | 15 | 29 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| t0002 | 0/0 | 636 | 48 | 37 | 6 | 0 | 3 | 2 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| t0003 | 0/0 | 632 | 21 | 2 | 3 | 13 | 0 | 3 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| t0004 | 0/0 | 636 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| t0005 | 0/0 | 636 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| t0006 | 0/0 | 636 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| 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 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0096 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0149 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2565 | 107 | 6 | 25 | 62 | 6 | 7 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0001c0002 | 0/0 | 2565 | 90 | 20 | 19 | 48 | 0 | 3 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0001c0010 | 0/0 | 2565 | 6 | 6 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0001c0013 | 0/0 | 2565 | 2 | 2 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0001c0021 | 0/0 | 2565 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0001c0023 | 0/0 | 2565 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0001c0028 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0002c0003 | 0/0 | 2565 | 50 | 14 | 4 | 15 | 4 | 13 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0002c0007 | 0/0 | 2565 | 10 | 0 | 0 | 10 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0002c0018 | 0/0 | 2565 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0002c0019 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0002c0027 | 0/0 | 2565 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0003c0004 | 0/0 | 2565 | 21 | 11 | 4 | 1 | 3 | 2 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0003c0009 | 0/0 | 2565 | 6 | 3 | 0 | 3 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0004c0005 | 0/0 | 2565 | 19 | 2 | 2 | 12 | 0 | 3 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0004c0015 | 0/0 | 2565 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0005c0006 | 1/0 | 2565 | 11 | 0 | 3 | 0 | 5 | 2 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0006c0008 | 0/0 | 2565 | 8 | 6 | 2 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0006c0020 | 0/0 | 2565 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0007c0011 | 0/0 | 2565 | 5 | 5 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0008c0012 | 0/0 | 2565 | 2 | 0 | 2 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0009c0024 | 0/0 | 2565 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0009c0026 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0010c0014 | 0/0 | 2565 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0011c0016 | 0/0 | 2565 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0012c0022 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0013c0025 | 0/0 | 2565 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0014c0017 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3200 | 106 | 6 | 24 | 62 | 6 | 7 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0001c0001t0003 | 0/0 | 3196 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0001c0002t0001 | 0/0 | 3200 | 66 | 0 | 16 | 47 | 0 | 3 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0001c0002t0002 | 0/0 | 3200 | 22 | 20 | 2 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0001c0002t0004 | 0/0 | 3200 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0001c0002t0006 | 0/0 | 3200 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0001c0010t0001 | 0/0 | 3200 | 6 | 6 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0001c0013t0001 | 0/0 | 3200 | 2 | 2 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0001c0021t0001 | 0/0 | 3200 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0001c0023t0001 | 0/0 | 3200 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0001c0028t0002 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0002c0003t0001 | 0/0 | 3200 | 48 | 13 | 4 | 15 | 4 | 12 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0002c0003t0002 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0002c0003t0003 | 0/0 | 3196 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0002c0007t0001 | 0/0 | 3200 | 10 | 0 | 0 | 10 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0002c0018t0001 | 0/0 | 3200 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0002c0019t0001 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0002c0027t0001 | 0/0 | 3200 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0003c0004t0001 | 0/0 | 3200 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0003c0004t0002 | 0/0 | 3200 | 19 | 10 | 4 | 0 | 3 | 2 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0003c0004t0005 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0003c0009t0001 | 0/0 | 3200 | 6 | 3 | 0 | 3 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0004c0005t0001 | 0/0 | 3200 | 3 | 0 | 0 | 1 | 0 | 2 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0004c0005t0003 | 0/0 | 3196 | 16 | 2 | 2 | 11 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0004c0015t0003 | 0/0 | 3196 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0005c0006t0001 | 1/0 | 3200 | 11 | 0 | 3 | 0 | 5 | 2 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0006c0008t0001 | 0/0 | 3200 | 8 | 6 | 2 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0006c0020t0003 | 0/0 | 3196 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0007c0011t0002 | 0/0 | 3200 | 5 | 5 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0008c0012t0001 | 0/0 | 3200 | 2 | 0 | 2 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0009c0024t0003 | 0/0 | 3196 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0009c0026t0001 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0010c0014t0001 | 0/0 | 3200 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0011c0016t0001 | 0/0 | 3200 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0012c0022t0001 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0013c0025t0001 | 0/0 | 3200 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| a0014c0017t0001 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | copy fasta | chr7 | 77305751 | 77421349 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0096 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0002t0006g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0010t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0010t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0010t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0010t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0010t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0010t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0013t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0013t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0021t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0023t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0001c0028t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0007t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0007t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0007t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0007t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0007t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0007t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0007t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0007t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0007t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0018t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0019t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0002c0027t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0004t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0009t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0009t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0009t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0009t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0009t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0003c0009t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0004c0005t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0004c0005t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0004c0005t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0004c0005t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0004c0005t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0004c0005t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0004c0005t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0004c0005t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0004c0005t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0004c0005t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0004c0005t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0004c0005t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0004c0005t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0004c0005t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0004c0005t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0004c0005t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0004c0005t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0004c0005t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0004c0005t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0004c0015t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0005c0006t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0005c0006t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0005c0006t0001g0149 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0005c0006t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0005c0006t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0005c0006t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0005c0006t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0005c0006t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0005c0006t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0005c0006t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0005c0006t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0006c0008t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0006c0008t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0006c0008t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0006c0008t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0006c0008t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0006c0008t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0006c0008t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0006c0008t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0006c0020t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0007c0011t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0007c0011t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0007c0011t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0007c0011t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0007c0011t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0008c0012t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0008c0012t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0009c0024t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0009c0026t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0010c0014t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0011c0016t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0012c0022t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0013c0025t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| a0014c0017t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0005 | c0006 | t0001 | g0132 | EUR | GBR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | GBR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00140 | hp1 | a0003 | c0004 | t0002 | g0125 | EUR | GBR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | GBR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | FIN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00280 | hp2 | a0002 | c0003 | t0001 | g0004 | EUR | FIN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00323 | hp1 | a0005 | c0006 | t0001 | g0169 | EUR | FIN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00323 | hp2 | a0002 | c0003 | t0001 | g0004 | EUR | FIN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0279 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00558 | hp2 | a0004 | c0005 | t0003 | g0160 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0300 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00621 | hp2 | a0004 | c0005 | t0003 | g0178 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00639 | hp1 | a0006 | c0008 | t0001 | g0142 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00642 | hp1 | a0003 | c0004 | t0002 | g0342 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00733 | hp2 | a0005 | c0006 | t0001 | g0123 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0245 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00738 | hp1 | a0008 | c0012 | t0001 | g0171 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0268 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0294 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0273 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01074 | hp1 | a0006 | c0008 | t0001 | g0137 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0272 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0343 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01099 | hp2 | a0013 | c0025 | t0001 | g0307 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01106 | hp1 | a0003 | c0004 | t0002 | g0341 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01109 | hp1 | a0005 | c0006 | t0001 | g0173 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01109 | hp2 | a0002 | c0027 | t0001 | g0215 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01167 | hp1 | a0004 | c0005 | t0003 | g0162 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0276 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0346 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01169 | hp1 | a0004 | c0005 | t0003 | g0159 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0344 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0345 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0131 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01243 | hp1 | a0001 | c0002 | t0004 | g0033 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01243 | hp2 | a0002 | c0003 | t0001 | g0287 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01255 | hp1 | a0005 | c0006 | t0001 | g0181 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01257 | hp2 | a0008 | c0012 | t0001 | g0170 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01258 | hp1 | a0003 | c0004 | t0002 | g0340 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01261 | hp1 | a0002 | c0003 | t0001 | g0148 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0238 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0302 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0129 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | IBS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01515 | hp2 | a0005 | c0006 | t0001 | g0168 | EUR | IBS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01516 | hp1 | a0002 | c0003 | t0001 | g0103 | EUR | IBS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01516 | hp2 | a0003 | c0004 | t0002 | g0204 | EUR | IBS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01517 | hp1 | a0005 | c0006 | t0001 | g0167 | EUR | IBS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01517 | hp2 | a0002 | c0003 | t0001 | g0104 | EUR | IBS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0220 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01884 | hp2 | a0002 | c0003 | t0001 | g0063 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01891 | hp1 | a0003 | c0004 | t0002 | g0133 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01891 | hp2 | a0007 | c0011 | t0002 | g0036 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0218 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0269 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0117 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01975 | hp2 | a0001 | c0021 | t0001 | g0250 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0284 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01993 | hp1 | a0003 | c0004 | t0002 | g0134 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02015 | hp2 | a0002 | c0003 | t0001 | g0336 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02027 | hp2 | a0009 | c0024 | t0003 | g0182 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02055 | hp1 | a0003 | c0004 | t0002 | g0187 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02055 | hp2 | a0004 | c0005 | t0003 | g0223 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02129 | hp1 | a0004 | c0005 | t0003 | g0116 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | CDX | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CDX | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | CDX | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | CDX | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0309 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02273 | hp2 | a0002 | c0003 | t0001 | g0058 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02280 | hp1 | a0006 | c0008 | t0001 | g0101 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02280 | hp2 | a0002 | c0003 | t0001 | g0313 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0013 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02451 | hp2 | a0002 | c0003 | t0001 | g0312 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02523 | hp2 | a0003 | c0004 | t0001 | g0191 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0208 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0321 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02622 | hp1 | a0006 | c0008 | t0001 | g0016 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02630 | hp2 | a0002 | c0003 | t0001 | g0212 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02683 | hp1 | a0002 | c0003 | t0001 | g0029 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02683 | hp2 | a0002 | c0018 | t0001 | g0100 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02717 | hp1 | a0003 | c0009 | t0001 | g0026 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0126 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02723 | hp1 | a0007 | c0011 | t0002 | g0145 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02723 | hp2 | a0006 | c0008 | t0001 | g0135 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02735 | hp1 | a0006 | c0020 | t0003 | g0023 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02738 | hp1 | a0001 | c0023 | t0001 | g0095 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02738 | hp2 | a0003 | c0004 | t0002 | g0114 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02809 | hp1 | a0001 | c0010 | t0001 | g0015 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02809 | hp2 | a0003 | c0009 | t0001 | g0028 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02886 | hp1 | a0006 | c0008 | t0001 | g0138 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02886 | hp2 | a0003 | c0004 | t0002 | g0339 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0225 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02896 | hp2 | a0002 | c0003 | t0001 | g0216 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02897 | hp1 | a0006 | c0008 | t0001 | g0140 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02897 | hp2 | a0002 | c0003 | t0001 | g0217 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0128 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02922 | hp2 | a0002 | c0003 | t0001 | g0062 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02965 | hp1 | a0003 | c0004 | t0002 | g0188 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02976 | hp1 | a0007 | c0011 | t0002 | g0311 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02976 | hp2 | a0012 | c0022 | t0001 | g0130 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03017 | hp1 | a0002 | c0003 | t0001 | g0059 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03017 | hp2 | a0004 | c0005 | t0001 | g0106 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03041 | hp1 | a0003 | c0004 | t0002 | g0147 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03041 | hp2 | a0003 | c0009 | t0001 | g0027 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03098 | hp1 | a0003 | c0004 | t0005 | g0186 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03098 | hp2 | a0003 | c0004 | t0002 | g0153 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03130 | hp1 | a0003 | c0004 | t0002 | g0184 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0109 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03139 | hp1 | a0001 | c0013 | t0001 | g0219 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03139 | hp2 | a0001 | c0010 | t0001 | g0150 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03195 | hp1 | a0007 | c0011 | t0002 | g0139 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03195 | hp2 | a0003 | c0004 | t0002 | g0185 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03209 | hp2 | a0002 | c0003 | t0001 | g0211 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0141 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03239 | hp1 | a0005 | c0006 | t0001 | g0166 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03453 | hp2 | a0009 | c0026 | t0001 | g0053 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03492 | hp1 | a0002 | c0003 | t0001 | g0121 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03516 | hp1 | a0001 | c0010 | t0001 | g0146 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03516 | hp2 | a0001 | c0013 | t0001 | g0222 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03579 | hp1 | a0002 | c0003 | t0002 | g0054 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0120 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03654 | hp1 | a0004 | c0005 | t0001 | g0107 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0266 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03669 | hp1 | a0002 | c0003 | t0001 | g0018 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03704 | hp1 | a0002 | c0003 | t0001 | g0156 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03704 | hp2 | a0002 | c0003 | t0001 | g0060 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0244 | SAS | BEB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0064 | SAS | BEB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03834 | hp1 | a0002 | c0003 | t0001 | g0079 | SAS | BEB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03834 | hp2 | a0004 | c0005 | t0003 | g0224 | SAS | BEB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03942 | hp2 | a0002 | c0003 | t0001 | g0065 | SAS | BEB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG04115 | hp2 | a0002 | c0003 | t0001 | g0066 | SAS | STU | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG04184 | hp1 | a0002 | c0003 | t0001 | g0068 | SAS | BEB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG04184 | hp2 | a0005 | c0006 | t0001 | g0207 | SAS | BEB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0119 | SAS | STU | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | STU | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG04204 | hp1 | a0002 | c0003 | t0003 | g0067 | SAS | STU | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG04204 | hp2 | a0002 | c0003 | t0001 | g0094 | SAS | STU | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18612 | hp1 | a0010 | c0014 | t0001 | g0174 | EAS | CHB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | CHB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18906 | hp1 | a0001 | c0010 | t0001 | g0152 | AFR | YRI | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18906 | hp2 | a0003 | c0004 | t0002 | g0154 | AFR | YRI | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18939 | hp2 | a0003 | c0009 | t0001 | g0189 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18940 | hp1 | a0002 | c0003 | t0001 | g0090 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18942 | hp1 | a0001 | c0002 | t0006 | g0006 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18943 | hp1 | a0004 | c0005 | t0003 | g0177 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18946 | hp2 | a0002 | c0007 | t0001 | g0338 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18949 | hp1 | a0002 | c0003 | t0001 | g0248 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18959 | hp2 | a0002 | c0003 | t0001 | g0122 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18961 | hp2 | a0002 | c0003 | t0001 | g0091 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18962 | hp2 | a0004 | c0005 | t0003 | g0164 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18963 | hp1 | a0002 | c0003 | t0001 | g0246 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18963 | hp2 | a0004 | c0005 | t0003 | g0289 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18964 | hp2 | a0004 | c0005 | t0003 | g0165 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18966 | hp1 | a0002 | c0003 | t0001 | g0288 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18967 | hp1 | a0002 | c0003 | t0001 | g0047 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18969 | hp1 | a0003 | c0009 | t0001 | g0190 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18971 | hp2 | a0002 | c0003 | t0001 | g0089 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18975 | hp2 | a0002 | c0003 | t0001 | g0057 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18978 | hp2 | a0002 | c0007 | t0001 | g0228 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18981 | hp1 | a0002 | c0007 | t0001 | g0324 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0319 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18983 | hp2 | a0002 | c0007 | t0001 | g0229 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18984 | hp1 | a0004 | c0015 | t0003 | g0176 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0337 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18997 | hp1 | a0003 | c0009 | t0001 | g0192 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19003 | hp1 | a0002 | c0003 | t0001 | g0286 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19030 | hp2 | a0002 | c0019 | t0001 | g0127 | AFR | LWK | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19043 | hp1 | a0007 | c0011 | t0002 | g0209 | AFR | LWK | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19043 | hp2 | a0006 | c0008 | t0001 | g0051 | AFR | LWK | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19054 | hp2 | a0004 | c0005 | t0003 | g0161 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19060 | hp1 | a0004 | c0005 | t0001 | g0172 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19062 | hp2 | a0002 | c0007 | t0001 | g0325 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19063 | hp2 | a0004 | c0005 | t0003 | g0163 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19064 | hp1 | a0004 | c0005 | t0003 | g0179 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19076 | hp1 | a0002 | c0003 | t0001 | g0020 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19077 | hp2 | a0002 | c0007 | t0001 | g0230 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19081 | hp1 | a0002 | c0007 | t0001 | g0323 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19084 | hp2 | a0002 | c0003 | t0001 | g0088 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19085 | hp1 | a0002 | c0007 | t0001 | g0003 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19085 | hp2 | a0002 | c0003 | t0001 | g0247 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19087 | hp1 | a0002 | c0007 | t0001 | g0003 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19090 | hp1 | a0002 | c0007 | t0001 | g0326 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19091 | hp1 | a0004 | c0005 | t0003 | g0175 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19091 | hp2 | a0002 | c0003 | t0001 | g0249 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19240 | hp1 | a0001 | c0028 | t0002 | g0143 | AFR | YRI | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA19240 | hp2 | a0001 | c0010 | t0001 | g0151 | AFR | YRI | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ASW | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA20129 | hp2 | a0002 | c0003 | t0001 | g0061 | AFR | ASW | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | TSI | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA20752 | hp2 | a0003 | c0004 | t0002 | g0124 | EUR | TSI | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA20805 | hp1 | a0005 | c0006 | t0001 | g0180 | EUR | TSI | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | TSI | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA20905 | hp1 | a0011 | c0016 | t0001 | g0038 | SAS | GIH | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA20905 | hp2 | a0003 | c0004 | t0002 | g0157 | SAS | GIH | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG01123 | hp2 | a0002 | c0003 | t0001 | g0102 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0108 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0221 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02486 | hp1 | a0002 | c0003 | t0001 | g0037 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02486 | hp2 | a0001 | c0010 | t0001 | g0025 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02559 | hp1 | a0002 | c0003 | t0001 | g0347 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0183 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0136 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG03471 | hp2 | a0002 | c0003 | t0001 | g0320 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG06807 | hp1 | a0003 | c0004 | t0002 | g0032 | AFR | USA | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| HG06807 | hp2 | a0004 | c0005 | t0003 | g0105 | AFR | USA | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | LWK | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| NA21309 | hp2 | a0014 | c0017 | t0001 | g0348 | AFR | LWK | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0096 | REF | REF | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| homoSapiens_grch38 | hp1 | a0005 | c0006 | t0001 | g0149 | REF | REF | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:77313523
|
T | G | 1 | a0013 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.2236A>C | p.Lys746Gln | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/31 | 2264/3200 | 2236/2565 | 746/854 | chr7 | 77313523 | ||
| chr7:77321369
|
C | A | 3 | a0004a0006a0009 | 31 | HG00558.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
missense_variant | MODERATE | c.1958G>T | p.Trp653Leu | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 25/31 | 1986/3200 | 1958/2565 | 653/854 | chr7 | 77321369 | ||
| chr7:77321382
|
C | T | 4 | a0003a0010a0012others(1): Show | 30 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(27): Show |
missense_variant | MODERATE | c.1945G>A | p.Val649Ile | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 25/31 | 1973/3200 | 1945/2565 | 649/854 | chr7 | 77321382 | ||
| chr7:77323718
|
A | T | 1 | a0007 | 5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
missense_variant | MODERATE | c.1852T>A | p.Phe618Ile | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/31 | 1880/3200 | 1852/2565 | 618/854 | chr7 | 77323718 | ||
| chr7:77362618
|
C | T | 5 | a0002a0003a0006others(2): Show | 106 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
missense_variant | MODERATE | c.914G>A | p.Gly305Glu | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/31 | 942/3200 | 914/2565 | 305/854 | chr7 | 77362618 | ||
| chr7:77382615
|
G | T | 1 | a0014 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.485C>A | p.Pro162His | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/31 | 513/3200 | 485/2565 | 162/854 | chr7 | 77382615 | ||
| chr7:77382617
|
A | T | 1 | a0014 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.483T>A | p.His161Gln | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/31 | 511/3200 | 483/2565 | 161/854 | chr7 | 77382617 | ||
| chr7:77406072
|
A | G | 1 | a0011 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.143T>C | p.Val48Ala | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/31 | 171/3200 | 143/2565 | 48/854 | chr7 | 77406072 | ||
| chr7:77406075
|
T | C | 10 | a0001a0002a0003others(7): Show | 318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
missense_variant | MODERATE | c.140A>G | p.His47Arg | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/31 | 168/3200 | 140/2565 | 47/854 | chr7 | 77406075 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:77311379
|
G | A | 1 | a0001c0010 | 6 | HG02486.hp2 HG02809.hp1 HG03139.hp2 others(3): Show |
synonymous_variant | LOW | c.2544C>T | p.Thr848Thr | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 31/31 | 2572/3200 | 2544/2565 | 848/854 | chr7 | 77311379 | ||
| chr7:77312128
|
C | T | 1 | a0001c0023 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.2346G>A | p.Thr782Thr | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 29/31 | 2374/3200 | 2346/2565 | 782/854 | chr7 | 77312128 | ||
| chr7:77314461
|
C | G | 5 | a0001c0013a0002c0019a0003c0009others(2): Show | 11 | HG02717.hp1 HG02809.hp2 HG02976.hp2 others(8): Show |
synonymous_variant | LOW | c.2118G>C | p.Gly706Gly | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/31 | 2146/3200 | 2118/2565 | 706/854 | chr7 | 77314461 | ||
| chr7:77353007
|
T | C | 1 | a0004c0015 | 1 | NA18984.hp1 | synonymous_variant | LOW | c.1428A>G | p.Val476Val | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/31 | 1456/3200 | 1428/2565 | 476/854 | chr7 | 77353007 | ||
| chr7:77355255
|
G | A | 16 | a0001c0002a0001c0013a0001c0021others(13): Show | 201 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(198): Show |
synonymous_variant | LOW | c.1296C>T | p.Cys432Cys | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/31 | 1324/3200 | 1296/2565 | 432/854 | chr7 | 77355255 | ||
| chr7:77360861
|
C | G | 12 | a0001c0021a0002c0003a0002c0007others(9): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
synonymous_variant | LOW | c.990G>C | p.Gly330Gly | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/31 | 1018/3200 | 990/2565 | 330/854 | chr7 | 77360861 | ||
| chr7:77374074
|
A | G | 1 | a0002c0007 | 10 | NA18946.hp2 NA18978.hp2 NA18981.hp1 others(7): Show |
synonymous_variant | LOW | c.867T>C | p.His289His | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/31 | 895/3200 | 867/2565 | 289/854 | chr7 | 77374074 | ||
| chr7:77381344
|
T | C | 3 | a0001c0028a0002c0027a0006c0008 | 10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
synonymous_variant | LOW | c.537A>G | p.Gln179Gln | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/31 | 565/3200 | 537/2565 | 179/854 | chr7 | 77381344 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:77310814
|
A | T | 1 | a0001c0002t0004 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*544T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 31/31 | 544 | chr7 | 77310814 | |||||
| chr7:77310814
|
AAAAT | A | 6 | a0001c0001t0003a0002c0003t0003a0004c0005t0003others(3): Show | 21 | HG00558.hp2 HG00621.hp2 HG01070.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*540_*543delATTT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 31/31 | 540 | chr7 | 77310814 | |||||
| chr7:77311211
|
T | C | 1 | a0001c0002t0006 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*147A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 31/31 | 147 | chr7 | 77311211 | |||||
| chr7:77311236
|
T | C | 1 | a0003c0004t0005 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*122A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 31/31 | 122 | chr7 | 77311236 | |||||
| chr7:77311296
|
A | G | 7 | a0001c0002t0002a0001c0002t0004a0001c0028t0002others(4): Show | 50 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*62T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 31/31 | 62 | chr7 | 77311296 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:77311477
|
A | G | 1 | a0001c0001t0001g0258 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2474-28T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 30/30 | chr7 | 77311477 | ||||||
| chr7:77311627
|
G | A | 9 | a0003c0004t0002g0114a0003c0004t0002g0124a0003c0004t0002g0125others(6): Show | 9 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.2474-178C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 30/30 | chr7 | 77311627 | ||||||
| chr7:77311677
|
TTTACTCT others(6): Show |
T | 1 | a0001c0001t0001g0199 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2473+151_2473+163d others(15): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 30/30 | chr7 | 77311677 | ||||||
| chr7:77311715
|
C | T | 13 | a0001c0002t0002g0136a0001c0002t0002g0141a0002c0003t0002g0054others(10): Show | 13 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2473+126G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 30/30 | chr7 | 77311715 | ||||||
| chr7:77311755
|
T | C | 2 | a0003c0004t0002g0032a0003c0004t0002g0339 | 2 | HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2473+86A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 30/30 | chr7 | 77311755 | ||||||
| chr7:77311972
|
A | G | 31 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0196others(28): Show | 32 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.2374-32T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 29/30 | chr7 | 77311972 | ||||||
| chr7:77312023
|
C | T | 13 | a0001c0013t0001g0219a0001c0013t0001g0222a0002c0019t0001g0127others(10): Show | 13 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.2373+78G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 29/30 | chr7 | 77312023 | ||||||
| chr7:77312046
|
C | T | 1 | a0001c0002t0001g0266 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2373+55G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 29/30 | chr7 | 77312046 | ||||||
| chr7:77312230
|
C | A | 147 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0031others(144): Show | 150 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.2272-28G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77312230 | ||||||
| chr7:77312232
|
A | AAT | 147 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0031others(144): Show | 150 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.2272-32_2272-31dup others(2): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77312232 | ||||||
| chr7:77312236
|
C | T | 1 | a0005c0006t0001g0207 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2272-34G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77312236 | ||||||
| chr7:77312513
|
C | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0031others(174): Show | 180 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.2272-311G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77312513 | ||||||
| chr7:77312567
|
C | T | 11 | a0001c0013t0001g0219a0001c0013t0001g0222a0002c0019t0001g0127others(8): Show | 11 | HG02717.hp1 HG02809.hp2 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.2272-365G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77312567 | ||||||
| chr7:77312879
|
C | T | 18 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0196others(15): Show | 19 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.2271+609G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77312879 | ||||||
| chr7:77312927
|
T | C | 4 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0334others(1): Show | 4 | HG00597.hp1 HG02015.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.2271+561A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77312927 | ||||||
| chr7:77312953
|
T | G | 2 | a0001c0001t0001g0335a0001c0002t0001g0240 | 2 | HG00544.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.2271+535A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77312953 | ||||||
| chr7:77312954
|
C | A | 1 | a0001c0002t0001g0240 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2271+534G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77312954 | ||||||
| chr7:77313010
|
C | T | 1 | a0001c0002t0001g0254 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2271+478G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77313010 | ||||||
| chr7:77313138
|
C | A | 75 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0042others(72): Show | 76 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.2271+350G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77313138 | ||||||
| chr7:77313287
|
C | CCT | 31 | a0001c0001t0003g0294a0002c0003t0003g0067a0004c0005t0001g0107others(28): Show | 31 | HG00558.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2271+200_2271+201i others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77313287 | ||||||
| chr7:77313289
|
A | T | 31 | a0001c0001t0003g0294a0002c0003t0003g0067a0004c0005t0001g0107others(28): Show | 31 | HG00558.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2271+199T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77313289 | ||||||
| chr7:77313327
|
A | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0031others(96): Show | 101 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.2271+161T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77313327 | ||||||
| chr7:77313345
|
G | T | 5 | a0001c0021t0001g0250a0002c0003t0001g0058a0002c0003t0001g0066others(2): Show | 5 | HG00733.hp2 HG01257.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.2271+143C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77313345 | ||||||
| chr7:77313425
|
G | A | 1 | a0002c0003t0001g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2271+63C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77313425 | ||||||
| chr7:77313469
|
A | T | 11 | a0002c0003t0002g0054a0003c0004t0002g0133a0003c0004t0002g0184others(8): Show | 11 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2271+19T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77313469 | ||||||
| chr7:77313624
|
G | C | 1 | a0002c0003t0001g0347 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2210-75C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77313624 | ||||||
| chr7:77313642
|
G | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0031others(92): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.2210-93C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77313642 | ||||||
| chr7:77313703
|
ACT | A | 10 | a0001c0013t0001g0219a0001c0013t0001g0222a0003c0009t0001g0026others(7): Show | 10 | HG02717.hp1 HG02809.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.2210-156_2210-155d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77313703 | ||||||
| chr7:77313921
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2210-372A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77313921 | ||||||
| chr7:77314026
|
T | G | 11 | a0002c0003t0002g0054a0003c0004t0002g0133a0003c0004t0002g0184others(8): Show | 11 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2209+344A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77314026 | ||||||
| chr7:77314041
|
T | A | 2 | a0003c0004t0002g0032a0003c0004t0002g0339 | 2 | HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2209+329A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77314041 | ||||||
| chr7:77314050
|
T | C | 21 | a0001c0002t0002g0001a0001c0002t0002g0126a0001c0002t0002g0131others(18): Show | 22 | HG01192.hp2 HG01884.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2209+320A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77314050 | ||||||
| chr7:77314135
|
T | C | 4 | a0001c0001t0001g0200a0001c0002t0001g0268a0001c0002t0001g0272others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.2209+235A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77314135 | ||||||
| chr7:77314149
|
C | A | 11 | a0001c0013t0001g0219a0001c0013t0001g0222a0002c0019t0001g0127others(8): Show | 11 | HG02717.hp1 HG02809.hp2 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.2209+221G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77314149 | ||||||
| chr7:77314154
|
T | C | 18 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0196others(15): Show | 19 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.2209+216A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77314154 | ||||||
| chr7:77314200
|
C | T | 46 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0050others(43): Show | 46 | HG00099.hp1 HG00733.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.2209+170G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77314200 | ||||||
| chr7:77314228
|
T | C | 2 | a0004c0005t0003g0160a0009c0024t0003g0182 | 2 | HG00558.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.2209+142A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77314228 | ||||||
| chr7:77314290
|
C | T | 1 | a0001c0001t0001g0317 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2209+80G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77314290 | ||||||
| chr7:77314810
|
C | G | 22 | a0001c0001t0003g0294a0002c0003t0003g0067a0004c0005t0001g0107others(19): Show | 22 | HG00558.hp2 HG00621.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.2090-321G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77314810 | ||||||
| chr7:77315059
|
G | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0042 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2090-570C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77315059 | ||||||
| chr7:77315239
|
G | A | 2 | a0001c0013t0001g0219a0001c0013t0001g0222 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2090-750C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77315239 | ||||||
| chr7:77315715
|
C | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0077 | 2 | NA19084.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2090-1226G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77315715 | ||||||
| chr7:77315896
|
G | A | 1 | a0001c0001t0001g0305 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2090-1407C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77315896 | ||||||
| chr7:77316399
|
G | A | 1 | a0003c0004t0001g0191 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2090-1910C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77316399 | ||||||
| chr7:77316429
|
GTC | G | 68 | a0001c0001t0001g0005a0001c0001t0001g0069a0001c0001t0001g0327others(65): Show | 69 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.2090-1942_2090-194 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77316429 | ||||||
| chr7:77316598
|
A | T | 1 | a0002c0003t0001g0047 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2090-2109T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77316598 | ||||||
| chr7:77316723
|
C | T | 31 | a0002c0003t0002g0054a0003c0004t0001g0191a0003c0004t0002g0032others(28): Show | 31 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.2090-2234G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77316723 | ||||||
| chr7:77316829
|
A | G | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2090-2340T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77316829 | ||||||
| chr7:77316879
|
A | G | 1 | a0002c0003t0001g0347 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2090-2390T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77316879 | ||||||
| chr7:77316883
|
C | T | 2 | a0005c0006t0001g0173a0005c0006t0001g0180 | 2 | HG01109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2090-2394G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77316883 | ||||||
| chr7:77316999
|
C | T | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2090-2510G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77316999 | ||||||
| chr7:77317116
|
T | TC | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2090-2628dupG | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317116 | ||||||
| chr7:77317153
|
C | T | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2090-2664G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317153 | ||||||
| chr7:77317200
|
G | A | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2090-2711C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317200 | ||||||
| chr7:77317239
|
C | T | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2090-2750G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317239 | ||||||
| chr7:77317295
|
A | G | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2090-2806T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317295 | ||||||
| chr7:77317304
|
C | T | 1 | a0001c0002t0001g0310 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2090-2815G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317304 | ||||||
| chr7:77317344
|
T | G | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2090-2855A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317344 | ||||||
| chr7:77317365
|
T | C | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2090-2876A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317365 | ||||||
| chr7:77317377
|
T | TGGGGTTG | 136 | a0001c0001t0001g0005a0001c0001t0001g0069a0001c0001t0001g0327others(133): Show | 138 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.2090-2895_2090-288 others(11): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317377 | ||||||
| chr7:77317655
|
G | C | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2089+3070C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317655 | ||||||
| chr7:77317775
|
C | A | 26 | a0002c0003t0002g0054a0003c0004t0001g0191a0003c0004t0002g0114others(23): Show | 26 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.2089+2950G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317775 | ||||||
| chr7:77317781
|
C | T | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2089+2944G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317781 | ||||||
| chr7:77317924
|
A | G | 17 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(14): Show | 18 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.2089+2801T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317924 | ||||||
| chr7:77317971
|
A | C | 30 | a0003c0004t0001g0191a0003c0004t0002g0032a0003c0004t0002g0114others(27): Show | 30 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.2089+2754T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317971 | ||||||
| chr7:77318155
|
A | G | 17 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(14): Show | 18 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.2089+2570T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318155 | ||||||
| chr7:77318202
|
C | T | 17 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(14): Show | 18 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.2089+2523G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318202 | ||||||
| chr7:77318284
|
C | G | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2089+2441G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318284 | ||||||
| chr7:77318342
|
A | AC | 17 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(14): Show | 18 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.2089+2382_2089+238 others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318342 | ||||||
| chr7:77318393
|
G | C | 17 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(14): Show | 18 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.2089+2332C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318393 | ||||||
| chr7:77318469
|
T | C | 1 | a0002c0003t0002g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2089+2256A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318469 | ||||||
| chr7:77318486
|
T | A | 17 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(14): Show | 18 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.2089+2239A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318486 | ||||||
| chr7:77318556
|
T | C | 17 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(14): Show | 18 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.2089+2169A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318556 | ||||||
| chr7:77318567
|
T | A | 47 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(44): Show | 48 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.2089+2158A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318567 | ||||||
| chr7:77318758
|
A | G | 17 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(14): Show | 18 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.2089+1967T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318758 | ||||||
| chr7:77318908
|
G | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0042 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2089+1817C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318908 | ||||||
| chr7:77318913
|
T | C | 30 | a0003c0004t0001g0191a0003c0004t0002g0032a0003c0004t0002g0114others(27): Show | 30 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.2089+1812A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318913 | ||||||
| chr7:77318954
|
G | A | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2089+1771C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318954 | ||||||
| chr7:77318965
|
A | G | 1 | a0001c0002t0001g0285 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2089+1760T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318965 | ||||||
| chr7:77319034
|
G | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0210others(46): Show | 50 | HG00099.hp1 HG00733.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.2089+1691C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77319034 | ||||||
| chr7:77319041
|
T | G | 30 | a0003c0004t0001g0191a0003c0004t0002g0032a0003c0004t0002g0114others(27): Show | 30 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.2089+1684A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77319041 | ||||||
| chr7:77319172
|
C | T | 1 | a0002c0003t0001g0249 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2089+1553G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77319172 | ||||||
| chr7:77319329
|
C | T | 2 | a0001c0002t0002g0108a0001c0002t0002g0109 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2089+1396G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77319329 | ||||||
| chr7:77319427
|
T | C | 226 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0069others(223): Show | 229 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.2089+1298A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77319427 | ||||||
| chr7:77319511
|
A | G | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2089+1214T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77319511 | ||||||
| chr7:77319655
|
T | C | 184 | a0001c0001t0001g0005a0001c0001t0001g0069a0001c0001t0001g0327others(181): Show | 187 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.2089+1070A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77319655 | ||||||
| chr7:77319758
|
T | TA | 153 | a0001c0001t0001g0005a0001c0001t0001g0069a0001c0001t0001g0327others(150): Show | 156 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.2089+966dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77319758 | ||||||
| chr7:77319846
|
A | G | 6 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2089+879T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77319846 | ||||||
| chr7:77319874
|
C | T | 88 | a0001c0001t0001g0014a0001c0002t0001g0276a0001c0002t0001g0343others(85): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.2089+851G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77319874 | ||||||
| chr7:77320025
|
C | CATGTT | 226 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0069others(223): Show | 229 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.2089+699_2089+700i others(7): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320025 | ||||||
| chr7:77320060
|
T | C | 1 | a0001c0002t0001g0310 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2089+665A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320060 | ||||||
| chr7:77320076
|
C | A | 226 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0069others(223): Show | 229 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.2089+649G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320076 | ||||||
| chr7:77320181
|
C | T | 2 | a0002c0003t0001g0059a0002c0003t0003g0067 | 2 | HG03017.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2089+544G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320181 | ||||||
| chr7:77320190
|
G | A | 12 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0112others(9): Show | 12 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.2089+535C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320190 | ||||||
| chr7:77320216
|
A | G | 342 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(339): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.2089+509T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320216 | ||||||
| chr7:77320423
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2089+302C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320423 | ||||||
| chr7:77320522
|
T | G | 1 | a0001c0002t0001g0242 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2089+203A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320522 | ||||||
| chr7:77320603
|
A | G | 22 | a0004c0005t0001g0106a0004c0005t0001g0107a0004c0005t0001g0172others(19): Show | 22 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.2089+122T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320603 | ||||||
| chr7:77320690
|
T | G | 1 | a0002c0003t0002g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2089+35A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320690 | ||||||
| chr7:77320698
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2089+27G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320698 | ||||||
| chr7:77320718
|
C | T | 42 | a0001c0001t0001g0014a0001c0002t0001g0343a0001c0002t0001g0344others(39): Show | 42 | HG00099.hp1 HG00733.hp2 HG01099.hp1 others(39): Show |
splice_region_variant&intron_variant | LOW | c.2089+7G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320718 | ||||||
| chr7:77320852
|
A | G | 4 | a0001c0001t0001g0327a0001c0002t0001g0218a0001c0002t0001g0235others(1): Show | 4 | HG01934.hp1 HG02165.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1995-33T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 25/30 | chr7 | 77320852 | ||||||
| chr7:77320913
|
T | C | 1 | a0003c0004t0001g0191 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1995-94A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 25/30 | chr7 | 77320913 | ||||||
| chr7:77320951
|
C | T | 8 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(5): Show | 8 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1995-132G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 25/30 | chr7 | 77320951 | ||||||
| chr7:77321263
|
A | G | 1 | a0007c0011t0002g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1994+70T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 25/30 | chr7 | 77321263 | ||||||
| chr7:77321273
|
T | C | 22 | a0003c0004t0001g0191a0003c0004t0002g0032a0003c0004t0002g0114others(19): Show | 22 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1994+60A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 25/30 | chr7 | 77321273 | ||||||
| chr7:77321560
|
C | T | 1 | a0002c0003t0002g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1924-157G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77321560 | ||||||
| chr7:77321581
|
T | C | 2 | a0001c0002t0002g0108a0001c0002t0002g0109 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1924-178A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77321581 | ||||||
| chr7:77321611
|
T | A | 57 | a0001c0002t0001g0276a0001c0002t0001g0343a0001c0002t0001g0344others(54): Show | 58 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1924-208A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77321611 | ||||||
| chr7:77321668
|
C | T | 130 | a0001c0001t0001g0005a0001c0001t0001g0069a0001c0001t0001g0327others(127): Show | 132 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.1924-265G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77321668 | ||||||
| chr7:77321859
|
T | A | 220 | a0001c0001t0001g0005a0001c0001t0001g0069a0001c0001t0001g0327others(217): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1924-456A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77321859 | ||||||
| chr7:77322323
|
G | A | 4 | a0003c0004t0002g0204a0003c0004t0002g0340a0003c0004t0002g0341others(1): Show | 4 | HG00642.hp1 HG01106.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1924-920C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322323 | ||||||
| chr7:77322401
|
C | T | 1 | a0002c0003t0001g0320 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1924-998G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322401 | ||||||
| chr7:77322462
|
T | C | 30 | a0003c0004t0001g0191a0003c0004t0002g0032a0003c0004t0002g0114others(27): Show | 30 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1924-1059A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322462 | ||||||
| chr7:77322582
|
G | GT | 17 | a0001c0001t0001g0031a0001c0001t0001g0071a0001c0001t0001g0078others(14): Show | 17 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.1923+1064dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322582 | ||||||
| chr7:77322582
|
GT | G | 112 | a0001c0001t0001g0005a0001c0001t0001g0069a0001c0001t0001g0293others(109): Show | 114 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1923+1064delA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322582 | ||||||
| chr7:77322591
|
T | G | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1923+1056A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322591 | ||||||
| chr7:77322604
|
T | A | 6 | a0001c0002t0001g0344a0001c0021t0001g0250a0002c0003t0001g0225others(3): Show | 6 | HG00099.hp1 HG01169.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1923+1043A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322604 | ||||||
| chr7:77322604
|
T | TA | 76 | a0001c0002t0001g0276a0001c0002t0001g0343a0001c0002t0001g0346others(73): Show | 77 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.1923+1042dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322604 | ||||||
| chr7:77322604
|
T | TTA | 6 | a0001c0002t0001g0345a0002c0003t0001g0047a0003c0004t0002g0133others(3): Show | 6 | HG01175.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1923+1042_1923+104 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322604 | ||||||
| chr7:77322948
|
C | A | 24 | a0003c0004t0001g0191a0003c0004t0002g0032a0003c0004t0002g0114others(21): Show | 24 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1923+699G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322948 | ||||||
| chr7:77322972
|
A | T | 30 | a0003c0004t0001g0191a0003c0004t0002g0032a0003c0004t0002g0114others(27): Show | 30 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1923+675T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322972 | ||||||
| chr7:77322986
|
GTTCT | G | 6 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1923+657_1923+660d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322986 | ||||||
| chr7:77322993
|
C | A | 1 | a0002c0003t0002g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1923+654G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322993 | ||||||
| chr7:77323000
|
T | C | 1 | a0004c0005t0003g0175 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1923+647A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77323000 | ||||||
| chr7:77323325
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0083 | 2 | HG03669.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1923+322T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77323325 | ||||||
| chr7:77323363
|
T | C | 5 | a0003c0004t0002g0032a0003c0004t0002g0147a0003c0004t0002g0153others(2): Show | 5 | HG02886.hp2 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1923+284A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77323363 | ||||||
| chr7:77323549
|
T | C | 9 | a0003c0004t0002g0114a0003c0004t0002g0124a0003c0004t0002g0125others(6): Show | 9 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1923+98A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77323549 | ||||||
| chr7:77323588
|
A | G | 8 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(5): Show | 8 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1923+59T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77323588 | ||||||
| chr7:77324000
|
C | T | 2 | a0001c0013t0001g0219a0001c0013t0001g0222 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1828-258G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324000 | ||||||
| chr7:77324007
|
C | A | 1 | a0002c0003t0001g0347 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1828-265G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324007 | ||||||
| chr7:77324042
|
A | C | 1 | a0001c0001t0001g0206 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1828-300T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324042 | ||||||
| chr7:77324122
|
A | G | 1 | a0001c0001t0001g0317 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1828-380T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324122 | ||||||
| chr7:77324168
|
G | C | 5 | a0007c0011t0002g0036a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1828-426C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324168 | ||||||
| chr7:77324174
|
C | G | 13 | a0003c0004t0001g0191a0003c0004t0002g0032a0003c0004t0002g0147others(10): Show | 13 | HG02523.hp2 HG02717.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.1828-432G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324174 | ||||||
| chr7:77324236
|
C | G | 25 | a0003c0004t0001g0191a0003c0004t0002g0114a0003c0004t0002g0124others(22): Show | 25 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1828-494G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324236 | ||||||
| chr7:77324468
|
T | C | 5 | a0007c0011t0002g0036a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1828-726A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324468 | ||||||
| chr7:77324536
|
A | G | 1 | a0001c0002t0002g0011 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1828-794T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324536 | ||||||
| chr7:77324576
|
G | C | 5 | a0007c0011t0002g0036a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1828-834C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324576 | ||||||
| chr7:77324615
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1828-873A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324615 | ||||||
| chr7:77324685
|
T | A | 1 | a0005c0006t0001g0207 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1828-943A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324685 | ||||||
| chr7:77324756
|
G | GT | 6 | a0001c0001t0001g0112a0001c0001t0001g0327a0001c0002t0001g0285others(3): Show | 6 | HG01175.hp1 HG04184.hp1 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.1828-1015dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324756 | ||||||
| chr7:77324825
|
ACT | A | 8 | a0001c0002t0001g0194a0001c0002t0001g0231a0001c0002t0001g0243others(5): Show | 8 | HG02071.hp2 HG02132.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1828-1085_1828-108 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324825 | ||||||
| chr7:77324826
|
C | CT | 68 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0259others(65): Show | 68 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.1828-1085dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324826 | ||||||
| chr7:77324826
|
C | CTT | 6 | a0001c0001t0001g0334a0001c0002t0002g0136a0001c0002t0002g0141others(3): Show | 6 | HG00621.hp2 HG02027.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1828-1086_1828-108 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324826 | ||||||
| chr7:77324826
|
CT | C | 109 | a0001c0001t0001g0005a0001c0001t0001g0193a0001c0001t0001g0327others(106): Show | 111 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1828-1085delA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324826 | ||||||
| chr7:77325024
|
T | C | 51 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(48): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1827+1188A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77325024 | ||||||
| chr7:77325027
|
G | A | 1 | a0002c0027t0001g0215 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1827+1185C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77325027 | ||||||
| chr7:77325404
|
C | G | 1 | a0002c0003t0002g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1827+808G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77325404 | ||||||
| chr7:77325407
|
A | G | 46 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(43): Show | 47 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.1827+805T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77325407 | ||||||
| chr7:77325439
|
T | C | 1 | a0001c0002t0001g0119 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1827+773A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77325439 | ||||||
| chr7:77326358
|
T | G | 1 | a0001c0002t0004g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1766-85A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77326358 | ||||||
| chr7:77326438
|
T | G | 31 | a0004c0005t0001g0106a0004c0005t0001g0107a0004c0005t0001g0172others(28): Show | 31 | HG00558.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.1766-165A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77326438 | ||||||
| chr7:77326445
|
A | C | 2 | a0001c0002t0002g0136a0001c0002t0002g0141 | 2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1766-172T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77326445 | ||||||
| chr7:77326446
|
G | C | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1766-173C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77326446 | ||||||
| chr7:77326627
|
C | T | 4 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(1): Show | 4 | HG01099.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1766-354G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77326627 | ||||||
| chr7:77326683
|
A | G | 46 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(43): Show | 47 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.1766-410T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77326683 | ||||||
| chr7:77326813
|
C | T | 46 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(43): Show | 47 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.1766-540G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77326813 | ||||||
| chr7:77326831
|
C | T | 1 | a0006c0020t0003g0023 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1766-558G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77326831 | ||||||
| chr7:77326930
|
T | G | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1766-657A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77326930 | ||||||
| chr7:77327007
|
G | A | 23 | a0004c0005t0001g0106a0004c0005t0001g0107a0004c0005t0001g0172others(20): Show | 23 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1766-734C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327007 | ||||||
| chr7:77327180
|
G | A | 2 | a0001c0010t0001g0146a0001c0010t0001g0150 | 2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1766-907C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327180 | ||||||
| chr7:77327280
|
C | T | 24 | a0003c0004t0001g0191a0003c0004t0002g0114a0003c0004t0002g0124others(21): Show | 24 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1766-1007G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327280 | ||||||
| chr7:77327322
|
G | A | 145 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(142): Show | 147 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1766-1049C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327322 | ||||||
| chr7:77327341
|
C | T | 1 | a0002c0003t0001g0347 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1766-1068G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327341 | ||||||
| chr7:77327370
|
A | AAC | 104 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(101): Show | 106 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.1766-1099_1766-109 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327370 | ||||||
| chr7:77327382
|
C | A | 1 | a0001c0001t0001g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1766-1109G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327382 | ||||||
| chr7:77327388
|
C | G | 1 | a0002c0003t0001g0121 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1766-1115G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327388 | ||||||
| chr7:77327457
|
T | C | 223 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(220): Show | 226 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.1765+1149A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327457 | ||||||
| chr7:77327502
|
C | T | 3 | a0007c0011t0002g0036a0007c0011t0002g0209a0007c0011t0002g0311 | 3 | HG01891.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1765+1104G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327502 | ||||||
| chr7:77327541
|
T | C | 1 | a0002c0003t0001g0065 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1765+1065A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327541 | ||||||
| chr7:77327605
|
CATAAAAC others(15): Show |
C | 9 | a0003c0004t0002g0114a0003c0004t0002g0124a0003c0004t0002g0125others(6): Show | 9 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1765+979_1765+1000 others(25): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327605 | ||||||
| chr7:77327637
|
C | T | 6 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1765+969G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327637 | ||||||
| chr7:77327723
|
T | C | 5 | a0007c0011t0002g0036a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1765+883A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327723 | ||||||
| chr7:77327730
|
C | T | 3 | a0002c0003t0001g0058a0002c0003t0001g0066a0008c0012t0001g0170 | 3 | HG01257.hp2 HG02273.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1765+876G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327730 | ||||||
| chr7:77327836
|
G | A | 23 | a0004c0005t0001g0106a0004c0005t0001g0107a0004c0005t0001g0172others(20): Show | 23 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1765+770C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327836 | ||||||
| chr7:77327871
|
G | C | 6 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1765+735C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327871 | ||||||
| chr7:77328228
|
G | A | 1 | a0002c0003t0001g0057 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1765+378C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77328228 | ||||||
| chr7:77328264
|
C | T | 41 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(38): Show | 41 | HG00099.hp1 HG00733.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.1765+342G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77328264 | ||||||
| chr7:77328360
|
C | T | 137 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(134): Show | 139 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.1765+246G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77328360 | ||||||
| chr7:77328434
|
A | T | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1765+172T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77328434 | ||||||
| chr7:77328447
|
G | A | 1 | a0007c0011t0002g0311 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1765+159C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77328447 | ||||||
| chr7:77328509
|
A | T | 32 | a0004c0005t0001g0106a0004c0005t0001g0107a0004c0005t0001g0172others(29): Show | 32 | HG00558.hp2 HG00621.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1765+97T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77328509 | ||||||
| chr7:77328794
|
T | C | 1 | a0001c0002t0001g0281 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1734-157A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 21/30 | chr7 | 77328794 | ||||||
| chr7:77329013
|
T | A | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1733+320A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 21/30 | chr7 | 77329013 | ||||||
| chr7:77329013
|
TA | T | 65 | a0001c0001t0001g0022a0001c0001t0001g0295a0001c0001t0003g0294others(62): Show | 65 | HG00099.hp1 HG00733.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.1733+319delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 21/30 | chr7 | 77329013 | ||||||
| chr7:77329048
|
C | A | 1 | a0001c0001t0001g0252 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1733+285G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 21/30 | chr7 | 77329048 | ||||||
| chr7:77329206
|
C | T | 5 | a0007c0011t0002g0036a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1733+127G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 21/30 | chr7 | 77329206 | ||||||
| chr7:77329240
|
A | G | 40 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(37): Show | 41 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.1733+93T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 21/30 | chr7 | 77329240 | ||||||
| chr7:77329408
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1675-17C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 20/30 | chr7 | 77329408 | ||||||
| chr7:77329413
|
A | G | 342 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(339): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1675-22T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 20/30 | chr7 | 77329413 | ||||||
| chr7:77329424
|
G | T | 6 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1675-33C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 20/30 | chr7 | 77329424 | ||||||
| chr7:77329634
|
G | C | 1 | a0001c0002t0002g0141 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1675-243C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 20/30 | chr7 | 77329634 | ||||||
| chr7:77329663
|
C | A | 102 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(99): Show | 104 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1675-272G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 20/30 | chr7 | 77329663 | ||||||
| chr7:77329708
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1675-317A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 20/30 | chr7 | 77329708 | ||||||
| chr7:77329786
|
C | CT | 87 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(84): Show | 89 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1675-396_1675-395i others(3): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 20/30 | chr7 | 77329786 | ||||||
| chr7:77329884
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1674+355G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 20/30 | chr7 | 77329884 | ||||||
| chr7:77330059
|
TAGG | T | 102 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(99): Show | 104 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1674+177_1674+179d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 20/30 | chr7 | 77330059 | ||||||
| chr7:77330150
|
T | C | 2 | a0002c0003t0001g0216a0002c0003t0001g0217 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1674+89A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 20/30 | chr7 | 77330150 | ||||||
| chr7:77330414
|
G | T | 101 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(98): Show | 103 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1546-47C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330414 | ||||||
| chr7:77330428
|
G | A | 1 | a0006c0008t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1546-61C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330428 | ||||||
| chr7:77330467
|
T | C | 101 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(98): Show | 103 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1546-100A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330467 | ||||||
| chr7:77330496
|
G | T | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1546-129C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330496 | ||||||
| chr7:77330498
|
A | G | 146 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(143): Show | 149 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.1546-131T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330498 | ||||||
| chr7:77330573
|
C | CT | 8 | a0001c0001t0001g0039a0001c0001t0001g0056a0001c0001t0001g0078others(5): Show | 8 | HG00099.hp2 HG00323.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1546-207dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330573 | ||||||
| chr7:77330573
|
CT | C | 8 | a0001c0001t0001g0072a0001c0001t0001g0113a0001c0001t0001g0227others(5): Show | 8 | HG00280.hp1 HG00609.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1546-207delA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330573 | ||||||
| chr7:77330578
|
T | G | 99 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0332others(96): Show | 101 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1546-211A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330578 | ||||||
| chr7:77330588
|
T | G | 2 | a0001c0002t0001g0284a0003c0004t0002g0147 | 2 | HG01981.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1546-221A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330588 | ||||||
| chr7:77330591
|
T | G | 101 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(98): Show | 103 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1546-224A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330591 | ||||||
| chr7:77330591
|
T | TG | 23 | a0002c0003t0001g0020a0003c0004t0001g0191a0003c0004t0002g0114others(20): Show | 23 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1546-225_1546-224i others(3): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330591 | ||||||
| chr7:77330591
|
T | TTG | 15 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0029others(12): Show | 16 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.1546-225_1546-224i others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330591 | ||||||
| chr7:77330591
|
T | TTTG | 7 | a0001c0002t0001g0276a0007c0011t0002g0036a0007c0011t0002g0139others(4): Show | 7 | HG01167.hp2 HG01891.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1546-227_1546-225d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330591 | ||||||
| chr7:77330696
|
C | T | 101 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(98): Show | 103 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1546-329G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330696 | ||||||
| chr7:77330788
|
T | C | 37 | a0004c0005t0001g0107a0004c0005t0001g0172a0004c0005t0003g0105others(34): Show | 37 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.1546-421A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330788 | ||||||
| chr7:77330805
|
C | T | 1 | a0001c0001t0001g0251 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1546-438G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330805 | ||||||
| chr7:77330866
|
A | G | 3 | a0002c0003t0001g0037a0002c0003t0001g0061a0002c0003t0001g0063 | 3 | HG01884.hp2 HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1546-499T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330866 | ||||||
| chr7:77330883
|
T | G | 45 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(42): Show | 46 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1546-516A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330883 | ||||||
| chr7:77331060
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1546-693A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77331060 | ||||||
| chr7:77331098
|
A | G | 109 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(106): Show | 111 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1546-731T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77331098 | ||||||
| chr7:77331257
|
T | C | 2 | a0002c0003t0001g0216a0002c0003t0001g0217 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1546-890A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77331257 | ||||||
| chr7:77331293
|
T | C | 1 | a0001c0002t0001g0243 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1546-926A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77331293 | ||||||
| chr7:77331502
|
G | A | 101 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(98): Show | 103 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1546-1135C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77331502 | ||||||
| chr7:77331567
|
C | T | 34 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(31): Show | 34 | HG00733.hp2 HG01099.hp1 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.1546-1200G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77331567 | ||||||
| chr7:77331800
|
T | C | 101 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(98): Show | 103 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1546-1433A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77331800 | ||||||
| chr7:77331892
|
G | GA | 22 | a0003c0004t0001g0191a0003c0004t0002g0114a0003c0004t0002g0124others(19): Show | 22 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1546-1526dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77331892 | ||||||
| chr7:77331892
|
GA | G | 135 | a0001c0001t0001g0113a0001c0001t0001g0255a0001c0001t0001g0306others(132): Show | 138 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1546-1526delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77331892 | ||||||
| chr7:77331894
|
A | G | 1 | a0002c0003t0001g0018 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1546-1527T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77331894 | ||||||
| chr7:77332007
|
A | G | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1546-1640T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77332007 | ||||||
| chr7:77332158
|
G | A | 1 | a0001c0002t0001g0285 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1546-1791C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77332158 | ||||||
| chr7:77332334
|
T | C | 29 | a0004c0005t0001g0106a0004c0005t0001g0107a0004c0005t0001g0172others(26): Show | 29 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.1546-1967A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77332334 | ||||||
| chr7:77332417
|
T | A | 45 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(42): Show | 46 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1546-2050A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77332417 | ||||||
| chr7:77332420
|
A | T | 5 | a0003c0004t0002g0032a0003c0004t0002g0147a0003c0004t0002g0153others(2): Show | 5 | HG02886.hp2 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1546-2053T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77332420 | ||||||
| chr7:77332564
|
G | A | 2 | a0002c0003t0001g0216a0002c0003t0001g0217 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1546-2197C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77332564 | ||||||
| chr7:77332617
|
G | A | 5 | a0007c0011t0002g0036a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-2250C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77332617 | ||||||
| chr7:77332968
|
A | G | 1 | a0001c0002t0001g0245 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1546-2601T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77332968 | ||||||
| chr7:77333080
|
A | T | 45 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(42): Show | 46 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1546-2713T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77333080 | ||||||
| chr7:77333116
|
A | G | 45 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(42): Show | 46 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1546-2749T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77333116 | ||||||
| chr7:77333140
|
G | A | 45 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(42): Show | 46 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1546-2773C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77333140 | ||||||
| chr7:77333551
|
C | G | 246 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0031others(243): Show | 250 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.1546-3184G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77333551 | ||||||
| chr7:77333688
|
T | C | 9 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(6): Show | 9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546-3321A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77333688 | ||||||
| chr7:77333803
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1546-3436A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77333803 | ||||||
| chr7:77334504
|
A | G | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1546-4137T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334504 | ||||||
| chr7:77334523
|
C | T | 5 | a0007c0011t0002g0036a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-4156G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334523 | ||||||
| chr7:77334579
|
T | TAAAAAAA others(3): Show |
1 | a0003c0004t0002g0133 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1546-4213_1546-421 others(14): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334579 | ||||||
| chr7:77334579
|
T | TAAAAAAA others(4): Show |
4 | a0003c0009t0001g0027a0003c0009t0001g0190a0003c0009t0001g0192others(1): Show | 4 | HG03041.hp2 NA18969.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1546-4213_1546-421 others(15): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334579 | ||||||
| chr7:77334579
|
T | TAAAAAAA others(5): Show |
9 | a0003c0004t0001g0191a0003c0004t0002g0114a0003c0004t0002g0204others(6): Show | 9 | HG00642.hp1 HG01106.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546-4213_1546-421 others(16): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334579 | ||||||
| chr7:77334579
|
T | TAAAAAAA others(6): Show |
2 | a0003c0004t0002g0124a0003c0004t0002g0125 | 2 | HG00140.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1546-4213_1546-421 others(17): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334579 | ||||||
| chr7:77334579
|
T | TAAAAAAA others(8): Show |
14 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(11): Show | 15 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.1546-4213_1546-421 others(19): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334579 | ||||||
| chr7:77334579
|
T | TAAAAAAA others(9): Show |
2 | a0002c0003t0001g0246a0002c0003t0001g0336 | 2 | HG02015.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1546-4213_1546-421 others(20): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334579 | ||||||
| chr7:77334579
|
T | TAAAAAAA others(10): Show |
2 | a0003c0004t0002g0134a0003c0004t0002g0157 | 2 | HG01993.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1546-4213_1546-421 others(21): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334579 | ||||||
| chr7:77334579
|
TTA | T | 4 | a0007c0011t0002g0036a0007c0011t0002g0139a0007c0011t0002g0145others(1): Show | 4 | HG01891.hp2 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1546-4214_1546-421 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334579 | ||||||
| chr7:77334580
|
T | A | 39 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(36): Show | 40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1546-4213A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334580 | ||||||
| chr7:77334580
|
T | TA | 49 | a0001c0001t0001g0049a0001c0001t0001g0085a0001c0001t0001g0098others(46): Show | 50 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.1546-4214dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334580 | ||||||
| chr7:77334580
|
T | TAA | 48 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0046others(45): Show | 49 | HG00733.hp2 HG01071.hp1 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546-4215_1546-421 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334580 | ||||||
| chr7:77334580
|
T | TAAA | 7 | a0001c0001t0001g0081a0002c0003t0001g0091a0002c0003t0001g0216others(4): Show | 7 | HG02896.hp2 HG02897.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1546-4216_1546-421 others(7): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334580 | ||||||
| chr7:77334580
|
TA | T | 27 | a0001c0001t0001g0007a0001c0001t0001g0035a0001c0001t0001g0056others(24): Show | 27 | HG00099.hp2 HG00408.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1546-4214delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334580 | ||||||
| chr7:77334797
|
A | G | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1546-4430T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334797 | ||||||
| chr7:77334851
|
G | A | 2 | a0001c0010t0001g0015a0001c0010t0001g0025 | 2 | HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1546-4484C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334851 | ||||||
| chr7:77334856
|
G | A | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1546-4489C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334856 | ||||||
| chr7:77334939
|
C | T | 40 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(37): Show | 41 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.1546-4572G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334939 | ||||||
| chr7:77335019
|
C | G | 1 | a0007c0011t0002g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1546-4652G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335019 | ||||||
| chr7:77335061
|
C | T | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305 | 3 | NA18966.hp2 NA18986.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1546-4694G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335061 | ||||||
| chr7:77335086
|
T | TA | 91 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(88): Show | 93 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1546-4720dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335086 | ||||||
| chr7:77335117
|
A | G | 9 | a0002c0007t0001g0003a0002c0007t0001g0228a0002c0007t0001g0229others(6): Show | 10 | NA18946.hp2 NA18978.hp2 NA18981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1546-4750T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335117 | ||||||
| chr7:77335182
|
T | C | 5 | a0007c0011t0002g0036a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-4815A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335182 | ||||||
| chr7:77335205
|
G | A | 5 | a0003c0004t0002g0032a0003c0004t0002g0147a0003c0004t0002g0153others(2): Show | 5 | HG02886.hp2 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1546-4838C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335205 | ||||||
| chr7:77335258
|
C | T | 1 | a0006c0008t0001g0138 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1546-4891G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335258 | ||||||
| chr7:77335356
|
C | A | 5 | a0007c0011t0002g0036a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-4989G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335356 | ||||||
| chr7:77335366
|
C | A | 1 | a0001c0001t0001g0329 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1546-4999G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335366 | ||||||
| chr7:77335454
|
C | G | 50 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(47): Show | 51 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.1546-5087G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335454 | ||||||
| chr7:77335455
|
A | G | 1 | a0002c0003t0002g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1546-5088T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335455 | ||||||
| chr7:77335623
|
T | C | 9 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(6): Show | 9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546-5256A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335623 | ||||||
| chr7:77335638
|
C | CA | 9 | a0001c0002t0001g0238a0003c0004t0002g0114a0003c0004t0002g0124others(6): Show | 9 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546-5272dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335638 | ||||||
| chr7:77335642
|
A | C | 1 | a0001c0002t0001g0304 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1546-5275T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335642 | ||||||
| chr7:77335809
|
G | A | 1 | a0002c0003t0001g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1546-5442C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335809 | ||||||
| chr7:77335826
|
C | G | 6 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1546-5459G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335826 | ||||||
| chr7:77336073
|
G | C | 22 | a0001c0001t0001g0332a0001c0002t0001g0117a0001c0002t0001g0233others(19): Show | 23 | HG00423.hp1 HG01433.hp1 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.1546-5706C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77336073 | ||||||
| chr7:77336132
|
C | T | 5 | a0007c0011t0002g0036a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-5765G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77336132 | ||||||
| chr7:77336176
|
T | C | 1 | a0002c0003t0001g0062 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1546-5809A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77336176 | ||||||
| chr7:77336379
|
C | T | 1 | a0004c0005t0001g0107 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1546-6012G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77336379 | ||||||
| chr7:77336481
|
C | CT | 55 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0046others(52): Show | 56 | HG00323.hp1 HG00733.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.1546-6115dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77336481 | ||||||
| chr7:77336485
|
T | G | 49 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(46): Show | 50 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1546-6118A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77336485 | ||||||
| chr7:77336614
|
A | G | 50 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(47): Show | 51 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.1546-6247T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77336614 | ||||||
| chr7:77336668
|
T | C | 1 | a0003c0004t0002g0153 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1546-6301A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77336668 | ||||||
| chr7:77336729
|
T | C | 50 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(47): Show | 51 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.1546-6362A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77336729 | ||||||
| chr7:77336790
|
T | C | 29 | a0004c0005t0001g0106a0004c0005t0001g0107a0004c0005t0001g0172others(26): Show | 29 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.1546-6423A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77336790 | ||||||
| chr7:77337143
|
C | T | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1546-6776G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77337143 | ||||||
| chr7:77337284
|
C | T | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1546-6917G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77337284 | ||||||
| chr7:77337285
|
G | A | 1 | a0001c0023t0001g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1546-6918C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77337285 | ||||||
| chr7:77337301
|
TG | T | 50 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(47): Show | 51 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.1546-6935delC | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77337301 | ||||||
| chr7:77337305
|
G | GGT | 91 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(88): Show | 93 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1546-6939_1546-693 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77337305 | ||||||
| chr7:77337309
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1546-6942C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77337309 | ||||||
| chr7:77337319
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1546-6952G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77337319 | ||||||
| chr7:77337701
|
C | A | 1 | a0001c0001t0003g0294 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1546-7334G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77337701 | ||||||
| chr7:77337758
|
A | G | 5 | a0007c0011t0002g0036a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-7391T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77337758 | ||||||
| chr7:77338051
|
A | C | 1 | a0002c0003t0001g0088 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1546-7684T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338051 | ||||||
| chr7:77338195
|
A | G | 7 | a0004c0005t0003g0223a0005c0006t0001g0132a0005c0006t0001g0166others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.1546-7828T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338195 | ||||||
| chr7:77338247
|
C | T | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1546-7880G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338247 | ||||||
| chr7:77338433
|
C | T | 50 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(47): Show | 51 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.1546-8066G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338433 | ||||||
| chr7:77338459
|
A | G | 1 | a0003c0004t0002g0134 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1546-8092T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338459 | ||||||
| chr7:77338559
|
A | C | 34 | a0003c0004t0001g0191a0003c0004t0002g0032a0003c0004t0002g0114others(31): Show | 34 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1546-8192T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338559 | ||||||
| chr7:77338621
|
G | A | 38 | a0004c0005t0001g0106a0004c0005t0001g0107a0004c0005t0001g0172others(35): Show | 38 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1546-8254C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338621 | ||||||
| chr7:77338641
|
G | A | 5 | a0001c0002t0002g0001a0001c0002t0002g0208a0001c0002t0002g0220others(2): Show | 6 | HG01884.hp1 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1546-8274C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338641 | ||||||
| chr7:77338652
|
G | A | 95 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(92): Show | 97 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.1546-8285C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338652 | ||||||
| chr7:77338800
|
A | T | 1 | a0006c0008t0001g0140 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1546-8433T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338800 | ||||||
| chr7:77338878
|
A | G | 1 | a0006c0020t0003g0023 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1546-8511T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338878 | ||||||
| chr7:77338925
|
A | C | 29 | a0003c0004t0001g0191a0003c0004t0002g0032a0003c0004t0002g0114others(26): Show | 29 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1546-8558T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338925 | ||||||
| chr7:77338948
|
A | G | 5 | a0007c0011t0002g0036a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-8581T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338948 | ||||||
| chr7:77339061
|
G | A | 1 | a0005c0006t0001g0123 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1546-8694C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339061 | ||||||
| chr7:77339064
|
A | G | 2 | a0002c0003t0001g0058a0002c0003t0001g0066 | 2 | HG02273.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1546-8697T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339064 | ||||||
| chr7:77339081
|
C | T | 90 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(87): Show | 92 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1546-8714G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339081 | ||||||
| chr7:77339149
|
A | C | 2 | a0006c0008t0001g0135a0006c0008t0001g0142 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1546-8782T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339149 | ||||||
| chr7:77339225
|
G | T | 1 | a0012c0022t0001g0130 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1546-8858C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339225 | ||||||
| chr7:77339278
|
G | A | 241 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0031others(238): Show | 245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1546-8911C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339278 | ||||||
| chr7:77339291
|
G | A | 4 | a0003c0004t0001g0191a0003c0009t0001g0189a0003c0009t0001g0190others(1): Show | 4 | HG02523.hp2 NA18939.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1546-8924C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339291 | ||||||
| chr7:77339331
|
G | A | 3 | a0001c0001t0001g0076a0001c0001t0001g0084a0005c0006t0001g0207 | 3 | HG04115.hp1 HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1546-8964C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339331 | ||||||
| chr7:77339353
|
C | G | 1 | a0011c0016t0001g0038 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1546-8986G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339353 | ||||||
| chr7:77339417
|
G | A | 1 | a0002c0003t0001g0064 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1546-9050C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339417 | ||||||
| chr7:77339424
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1546-9057C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339424 | ||||||
| chr7:77339586
|
A | G | 29 | a0003c0004t0001g0191a0003c0004t0002g0032a0003c0004t0002g0114others(26): Show | 29 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1546-9219T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339586 | ||||||
| chr7:77339621
|
A | C | 1 | a0004c0005t0003g0116 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1546-9254T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339621 | ||||||
| chr7:77339643
|
A | G | 4 | a0006c0008t0001g0051a0006c0008t0001g0135a0006c0008t0001g0138others(1): Show | 4 | HG00639.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1546-9276T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339643 | ||||||
| chr7:77339671
|
A | AGGAGGAC others(10): Show |
90 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(87): Show | 92 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1546-9321_1546-930 others(21): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339671 | ||||||
| chr7:77339688
|
T | TGGAGGAC others(10): Show |
10 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(7): Show | 10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1546-9322_1546-932 others(21): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339688 | ||||||
| chr7:77339712
|
TAC | T | 90 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(87): Show | 92 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1546-9347_1546-934 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339712 | ||||||
| chr7:77339737
|
A | T | 1 | a0002c0003t0001g0286 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1546-9370T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339737 | ||||||
| chr7:77340034
|
T | G | 1 | a0001c0002t0001g0245 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1545+9317A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77340034 | ||||||
| chr7:77340175
|
C | A | 9 | a0006c0008t0001g0016a0006c0008t0001g0051a0006c0008t0001g0101others(6): Show | 9 | HG00639.hp1 HG01074.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1545+9176G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77340175 | ||||||
| chr7:77340232
|
C | T | 10 | a0001c0002t0001g0239a0002c0007t0001g0003a0002c0007t0001g0228others(7): Show | 11 | HG02027.hp1 NA18946.hp2 NA18978.hp2 others(8): Show |
intron_variant | MODIFIER | c.1545+9119G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77340232 | ||||||
| chr7:77340378
|
C | T | 5 | a0001c0002t0001g0019a0001c0002t0001g0024a0001c0002t0001g0298others(2): Show | 5 | HG00609.hp1 NA18940.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.1545+8973G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77340378 | ||||||
| chr7:77340414
|
G | A | 1 | a0001c0002t0001g0119 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1545+8937C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77340414 | ||||||
| chr7:77340517
|
G | A | 24 | a0003c0004t0001g0191a0003c0004t0002g0114a0003c0004t0002g0124others(21): Show | 24 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1545+8834C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77340517 | ||||||
| chr7:77340522
|
T | C | 110 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(107): Show | 112 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.1545+8829A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77340522 | ||||||
| chr7:77340795
|
A | C | 90 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(87): Show | 92 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1545+8556T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77340795 | ||||||
| chr7:77340858
|
C | T | 9 | a0006c0008t0001g0016a0006c0008t0001g0051a0006c0008t0001g0101others(6): Show | 9 | HG00639.hp1 HG01074.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1545+8493G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77340858 | ||||||
| chr7:77340999
|
T | G | 24 | a0003c0004t0001g0191a0003c0004t0002g0114a0003c0004t0002g0124others(21): Show | 24 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1545+8352A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77340999 | ||||||
| chr7:77341059
|
T | C | 244 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0031others(241): Show | 248 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1545+8292A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77341059 | ||||||
| chr7:77341115
|
A | G | 1 | a0004c0005t0003g0165 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1545+8236T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77341115 | ||||||
| chr7:77341160
|
C | T | 24 | a0003c0004t0001g0191a0003c0004t0002g0114a0003c0004t0002g0124others(21): Show | 24 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1545+8191G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77341160 | ||||||
| chr7:77341181
|
T | G | 6 | a0002c0003t0002g0054a0003c0004t0002g0032a0003c0004t0002g0147others(3): Show | 6 | HG02886.hp2 HG03041.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1545+8170A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77341181 | ||||||
| chr7:77341188
|
T | A | 7 | a0001c0002t0002g0001a0001c0002t0002g0208a0001c0002t0002g0220others(4): Show | 8 | HG01884.hp1 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1545+8163A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77341188 | ||||||
| chr7:77341386
|
A | C | 9 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(6): Show | 9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1545+7965T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77341386 | ||||||
| chr7:77341457
|
G | A | 1 | a0003c0004t0002g0124 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1545+7894C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77341457 | ||||||
| chr7:77341751
|
C | T | 1 | a0003c0004t0002g0153 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1545+7600G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77341751 | ||||||
| chr7:77341914
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1545+7437G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77341914 | ||||||
| chr7:77341983
|
C | G | 1 | a0005c0006t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1545+7368G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77341983 | ||||||
| chr7:77342079
|
G | A | 5 | a0007c0011t0002g0036a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1545+7272C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342079 | ||||||
| chr7:77342125
|
TCTGA | T | 9 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(6): Show | 9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1545+7222_1545+722 others(8): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342125 | ||||||
| chr7:77342161
|
G | A | 118 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(115): Show | 120 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1545+7190C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342161 | ||||||
| chr7:77342201
|
T | C | 1 | a0002c0003t0001g0246 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1545+7150A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342201 | ||||||
| chr7:77342202
|
G | T | 1 | a0002c0003t0001g0246 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1545+7149C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342202 | ||||||
| chr7:77342224
|
C | T | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1545+7127G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342224 | ||||||
| chr7:77342249
|
T | C | 129 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(126): Show | 131 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1545+7102A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342249 | ||||||
| chr7:77342269
|
C | T | 1 | a0002c0003t0002g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1545+7082G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342269 | ||||||
| chr7:77342452
|
T | C | 129 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(126): Show | 131 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1545+6899A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342452 | ||||||
| chr7:77342459
|
A | C | 8 | a0002c0003t0001g0018a0002c0003t0001g0020a0002c0003t0001g0029others(5): Show | 8 | HG02015.hp2 HG02683.hp1 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.1545+6892T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342459 | ||||||
| chr7:77342495
|
T | C | 1 | a0002c0003t0001g0057 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1545+6856A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342495 | ||||||
| chr7:77342531
|
T | TC | 39 | a0004c0005t0001g0106a0004c0005t0001g0107a0004c0005t0001g0172others(36): Show | 39 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1545+6819dupG | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342531 | ||||||
| chr7:77342535
|
T | C | 39 | a0004c0005t0001g0106a0004c0005t0001g0107a0004c0005t0001g0172others(36): Show | 39 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1545+6816A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342535 | ||||||
| chr7:77342618
|
G | A | 1 | a0002c0018t0001g0100 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1545+6733C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342618 | ||||||
| chr7:77342624
|
T | C | 1 | a0001c0002t0001g0310 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1545+6727A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342624 | ||||||
| chr7:77342819
|
G | T | 1 | a0002c0003t0001g0246 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1545+6532C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342819 | ||||||
| chr7:77342824
|
C | T | 1 | a0001c0002t0001g0278 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1545+6527G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342824 | ||||||
| chr7:77342873
|
A | G | 105 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(102): Show | 107 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.1545+6478T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342873 | ||||||
| chr7:77343058
|
A | G | 242 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0031others(239): Show | 246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1545+6293T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77343058 | ||||||
| chr7:77343184
|
G | A | 1 | a0001c0001t0001g0331 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1545+6167C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77343184 | ||||||
| chr7:77343185
|
C | CT | 105 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0327others(102): Show | 107 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.1545+6165_1545+616 others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77343185 | ||||||
| chr7:77343251
|
T | G | 6 | a0002c0003t0002g0054a0003c0004t0002g0032a0003c0004t0002g0147others(3): Show | 6 | HG02886.hp2 HG03041.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1545+6100A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77343251 | ||||||
| chr7:77343568
|
G | A | 16 | a0003c0004t0001g0191a0003c0004t0002g0114a0003c0004t0002g0124others(13): Show | 16 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1545+5783C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77343568 | ||||||
| chr7:77343801
|
A | G | 149 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0001t0001g0332others(146): Show | 152 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1545+5550T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77343801 | ||||||
| chr7:77343861
|
C | T | 2 | a0002c0003t0001g0091a0012c0022t0001g0130 | 2 | HG02976.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.1545+5490G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77343861 | ||||||
| chr7:77344069
|
A | G | 24 | a0003c0004t0001g0191a0003c0004t0002g0114a0003c0004t0002g0124others(21): Show | 24 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1545+5282T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77344069 | ||||||
| chr7:77344406
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1545+4945C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77344406 | ||||||
| chr7:77344523
|
G | A | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1545+4828C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77344523 | ||||||
| chr7:77344589
|
G | GT | 347 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(344): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1545+4761dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77344589 | ||||||
| chr7:77344763
|
A | C | 117 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0002t0001g0019others(114): Show | 118 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1545+4588T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77344763 | ||||||
| chr7:77344906
|
C | T | 6 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1545+4445G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77344906 | ||||||
| chr7:77345108
|
T | C | 2 | a0006c0008t0001g0138a0007c0011t0002g0139 | 2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1545+4243A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345108 | ||||||
| chr7:77345231
|
G | C | 117 | a0001c0001t0001g0005a0001c0001t0001g0259a0001c0001t0001g0306others(114): Show | 118 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1545+4120C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345231 | ||||||
| chr7:77345502
|
G | A | 2 | a0003c0004t0002g0341a0003c0004t0002g0342 | 2 | HG00642.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1545+3849C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345502 | ||||||
| chr7:77345572
|
A | T | 53 | a0001c0001t0001g0002a0001c0001t0001g0210a0001c0001t0001g0251others(50): Show | 55 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1545+3779T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345572 | ||||||
| chr7:77345689
|
C | T | 16 | a0001c0002t0001g0276a0002c0003t0001g0004a0002c0003t0001g0018others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1545+3662G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345689 | ||||||
| chr7:77345690
|
C | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0210a0001c0001t0001g0251others(47): Show | 52 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.1545+3661G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345690 | ||||||
| chr7:77345692
|
C | T | 1 | a0002c0003t0001g0246 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1545+3659G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345692 | ||||||
| chr7:77345696
|
T | C | 116 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0002t0001g0019others(113): Show | 117 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1545+3655A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345696 | ||||||
| chr7:77345839
|
C | G | 6 | a0002c0003t0002g0054a0007c0011t0002g0036a0007c0011t0002g0139others(3): Show | 6 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1545+3512G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345839 | ||||||
| chr7:77345870
|
C | T | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1545+3481G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345870 | ||||||
| chr7:77345963
|
T | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0210a0001c0001t0001g0251others(50): Show | 55 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1545+3388A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345963 | ||||||
| chr7:77346067
|
C | T | 1 | a0002c0018t0001g0100 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1545+3284G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346067 | ||||||
| chr7:77346252
|
G | A | 87 | a0001c0001t0001g0005a0001c0002t0001g0019a0001c0002t0001g0024others(84): Show | 88 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1545+3099C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346252 | ||||||
| chr7:77346265
|
C | T | 2 | a0001c0002t0001g0158a0001c0002t0001g0240 | 2 | HG00544.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.1545+3086G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346265 | ||||||
| chr7:77346270
|
C | CA | 10 | a0001c0001t0001g0213a0001c0001t0001g0316a0001c0002t0001g0276others(7): Show | 10 | HG00738.hp2 HG01074.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1545+3080dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346270 | ||||||
| chr7:77346270
|
C | CAAAA | 8 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0011others(5): Show | 8 | HG01433.hp2 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1545+3077_1545+308 others(8): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346270 | ||||||
| chr7:77346270
|
C | CAAAAA | 26 | a0001c0002t0006g0006a0003c0004t0001g0191a0003c0004t0002g0032others(23): Show | 26 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1545+3076_1545+308 others(9): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346270 | ||||||
| chr7:77346270
|
C | CAAAAAAA | 63 | a0001c0001t0001g0005a0001c0002t0001g0019a0001c0002t0001g0024others(60): Show | 64 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.1545+3074_1545+308 others(11): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346270 | ||||||
| chr7:77346270
|
C | CAAAAAAA others(1): Show |
10 | a0001c0002t0001g0111a0001c0002t0001g0234a0001c0002t0001g0235others(7): Show | 10 | HG01952.hp1 HG03516.hp2 NA18612.hp2 others(7): Show |
intron_variant | MODIFIER | c.1545+3073_1545+308 others(12): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346270 | ||||||
| chr7:77346270
|
CA | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0306a0001c0001t0001g0314others(4): Show | 7 | HG01070.hp2 HG03704.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.1545+3080delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346270 | ||||||
| chr7:77346287
|
A | G | 1 | a0005c0006t0001g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1545+3064T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346287 | ||||||
| chr7:77346311
|
T | A | 121 | a0001c0001t0001g0005a0001c0002t0001g0019a0001c0002t0001g0024others(118): Show | 122 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1545+3040A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346311 | ||||||
| chr7:77346377
|
C | A | 1 | a0001c0023t0001g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1545+2974G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346377 | ||||||
| chr7:77346537
|
C | CA | 85 | a0001c0001t0001g0005a0001c0001t0001g0048a0001c0001t0001g0074others(82): Show | 86 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1545+2813dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346537 | ||||||
| chr7:77346621
|
G | A | 40 | a0004c0005t0001g0106a0004c0005t0001g0107a0004c0005t0001g0172others(37): Show | 40 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1545+2730C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346621 | ||||||
| chr7:77346659
|
G | A | 11 | a0001c0001t0001g0031a0001c0001t0001g0046a0001c0001t0001g0048others(8): Show | 11 | HG00323.hp1 HG01934.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.1545+2692C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346659 | ||||||
| chr7:77346717
|
GAA | G | 86 | a0001c0001t0001g0005a0001c0002t0001g0019a0001c0002t0001g0024others(83): Show | 87 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.1545+2632_1545+263 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346717 | ||||||
| chr7:77346757
|
T | C | 86 | a0001c0001t0001g0005a0001c0002t0001g0019a0001c0002t0001g0024others(83): Show | 87 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.1545+2594A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346757 | ||||||
| chr7:77346867
|
G | A | 1 | a0004c0005t0003g0177 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1545+2484C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346867 | ||||||
| chr7:77346872
|
A | ACT | 244 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0031others(241): Show | 248 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1545+2477_1545+247 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346872 | ||||||
| chr7:77346934
|
A | ACCACCAC others(8): Show |
1 | a0001c0001t0001g0259 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1545+2402_1545+241 others(19): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346934 | ||||||
| chr7:77346950
|
C | A | 1 | a0001c0001t0001g0113 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1545+2401G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346950 | ||||||
| chr7:77347004
|
T | C | 87 | a0001c0001t0001g0005a0001c0002t0001g0019a0001c0002t0001g0024others(84): Show | 88 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1545+2347A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347004 | ||||||
| chr7:77347204
|
G | T | 6 | a0002c0003t0002g0054a0007c0011t0002g0036a0007c0011t0002g0139others(3): Show | 6 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1545+2147C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347204 | ||||||
| chr7:77347295
|
G | A | 1 | a0001c0001t0001g0306 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1545+2056C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347295 | ||||||
| chr7:77347416
|
G | A | 1 | a0002c0003t0001g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1545+1935C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347416 | ||||||
| chr7:77347517
|
T | C | 40 | a0004c0005t0001g0106a0004c0005t0001g0107a0004c0005t0001g0172others(37): Show | 40 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1545+1834A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347517 | ||||||
| chr7:77347704
|
A | G | 6 | a0002c0003t0002g0054a0007c0011t0002g0036a0007c0011t0002g0139others(3): Show | 6 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1545+1647T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347704 | ||||||
| chr7:77347798
|
G | A | 1 | a0001c0002t0001g0245 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1545+1553C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347798 | ||||||
| chr7:77347822
|
T | G | 2 | a0001c0002t0002g0136a0001c0002t0002g0141 | 2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1545+1529A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347822 | ||||||
| chr7:77347854
|
T | C | 2 | a0002c0003t0001g0248a0002c0003t0001g0288 | 2 | NA18949.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1545+1497A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347854 | ||||||
| chr7:77347893
|
T | C | 1 | a0001c0001t0001g0007 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1545+1458A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347893 | ||||||
| chr7:77347987
|
C | CA | 43 | a0001c0001t0001g0084a0001c0001t0001g0305a0001c0001t0001g0327others(40): Show | 43 | HG00099.hp1 HG00558.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1545+1363dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347987 | ||||||
| chr7:77347987
|
CA | C | 20 | a0001c0001t0001g0056a0001c0001t0001g0078a0001c0002t0001g0274others(17): Show | 21 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1545+1363delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347987 | ||||||
| chr7:77348000
|
A | T | 123 | a0001c0001t0001g0005a0001c0002t0001g0019a0001c0002t0001g0024others(120): Show | 124 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.1545+1351T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348000 | ||||||
| chr7:77348003
|
T | A | 3 | a0005c0006t0001g0132a0005c0006t0001g0167a0005c0006t0001g0168 | 3 | HG00099.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1545+1348A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348003 | ||||||
| chr7:77348113
|
G | A | 1 | a0001c0001t0001g0293 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1545+1238C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348113 | ||||||
| chr7:77348152
|
A | G | 1 | a0002c0003t0001g0320 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1545+1199T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348152 | ||||||
| chr7:77348502
|
G | A | 5 | a0001c0002t0001g0239a0001c0002t0001g0265a0001c0002t0001g0275others(2): Show | 5 | HG00673.hp1 HG01099.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1545+849C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348502 | ||||||
| chr7:77348596
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1545+755C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348596 | ||||||
| chr7:77348768
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1545+583C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348768 | ||||||
| chr7:77348779
|
G | A | 7 | a0005c0006t0001g0132a0005c0006t0001g0166a0005c0006t0001g0167others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1545+572C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348779 | ||||||
| chr7:77348936
|
C | CTG | 20 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0002t0001g0019others(17): Show | 20 | HG00733.hp2 HG01433.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1545+413_1545+414d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348936 | ||||||
| chr7:77348936
|
CTGTG | C | 3 | a0001c0001t0001g0260a0001c0013t0001g0219a0001c0013t0001g0222 | 3 | HG00609.hp2 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1545+411_1545+414d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348936 | ||||||
| chr7:77348967
|
C | T | 75 | a0001c0001t0001g0005a0001c0002t0001g0019a0001c0002t0001g0024others(72): Show | 76 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1545+384G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348967 | ||||||
| chr7:77349203
|
T | G | 9 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(6): Show | 9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1545+148A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77349203 | ||||||
| chr7:77349259
|
A | G | 6 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1545+92T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77349259 | ||||||
| chr7:77349277
|
A | G | 1 | a0001c0001t0001g0007 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1545+74T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77349277 | ||||||
| chr7:77349459
|
G | C | 1 | a0001c0001t0001g0195 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1492-55C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77349459 | ||||||
| chr7:77349560
|
G | A | 9 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(6): Show | 9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1492-156C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77349560 | ||||||
| chr7:77349590
|
A | G | 228 | a0001c0001t0001g0005a0001c0002t0001g0019a0001c0002t0001g0024others(225): Show | 231 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1492-186T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77349590 | ||||||
| chr7:77349667
|
TAGAG | T | 29 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(26): Show | 29 | HG00140.hp1 HG00642.hp1 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.1492-267_1492-264d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77349667 | ||||||
| chr7:77349709
|
C | T | 1 | a0003c0004t0002g0204 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1492-305G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77349709 | ||||||
| chr7:77349736
|
A | C | 3 | a0001c0001t0001g0014a0001c0010t0001g0015a0001c0010t0001g0025 | 3 | HG02486.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1492-332T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77349736 | ||||||
| chr7:77349779
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1492-375G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77349779 | ||||||
| chr7:77349970
|
C | T | 1 | a0001c0002t0001g0238 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1492-566G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77349970 | ||||||
| chr7:77349971
|
G | A | 9 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(6): Show | 9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1492-567C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77349971 | ||||||
| chr7:77350036
|
A | G | 1 | a0001c0002t0001g0270 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1492-632T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350036 | ||||||
| chr7:77350285
|
A | G | 14 | a0001c0002t0001g0119a0001c0002t0001g0158a0001c0002t0001g0240others(11): Show | 14 | HG00544.hp2 HG00558.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1492-881T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350285 | ||||||
| chr7:77350285
|
AG | A | 71 | a0001c0001t0001g0005a0001c0002t0001g0019a0001c0002t0001g0024others(68): Show | 72 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1492-882delC | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350285 | ||||||
| chr7:77350286
|
G | A | 13 | a0001c0002t0001g0119a0001c0002t0001g0158a0001c0002t0001g0240others(10): Show | 13 | HG00544.hp2 HG00558.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1492-882C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350286 | ||||||
| chr7:77350293
|
G | A | 1 | a0002c0003t0001g0121 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1492-889C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350293 | ||||||
| chr7:77350471
|
C | T | 31 | a0004c0005t0001g0106a0004c0005t0001g0107a0004c0005t0001g0172others(28): Show | 31 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1492-1067G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350471 | ||||||
| chr7:77350472
|
G | C | 23 | a0001c0002t0002g0136a0001c0002t0002g0141a0003c0004t0001g0191others(20): Show | 23 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1492-1068C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350472 | ||||||
| chr7:77350572
|
T | TA | 119 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(116): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.1492-1169dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350572 | ||||||
| chr7:77350572
|
T | TAA | 14 | a0002c0003t0001g0059a0002c0003t0001g0064a0002c0003t0001g0091others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1492-1170_1492-116 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350572 | ||||||
| chr7:77350572
|
TA | T | 92 | a0001c0001t0001g0005a0001c0001t0001g0092a0001c0001t0001g0196others(89): Show | 93 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1492-1169delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350572 | ||||||
| chr7:77350616
|
G | A | 2 | a0002c0003t0001g0211a0002c0003t0001g0212 | 2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1492-1212C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350616 | ||||||
| chr7:77350925
|
T | A | 3 | a0001c0002t0001g0268a0001c0002t0001g0272a0001c0002t0001g0273 | 3 | HG01069.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1492-1521A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350925 | ||||||
| chr7:77350947
|
T | C | 16 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0020others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1492-1543A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350947 | ||||||
| chr7:77351009
|
A | T | 1 | a0001c0001t0001g0080 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1492-1605T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77351009 | ||||||
| chr7:77351091
|
C | A | 1 | a0001c0001t0001g0293 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1492-1687G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77351091 | ||||||
| chr7:77351147
|
A | G | 2 | a0002c0003t0001g0211a0002c0003t0001g0212 | 2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1492-1743T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77351147 | ||||||
| chr7:77351324
|
AGGGCATC others(4): Show |
A | 144 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(141): Show | 146 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1491+1609_1491+161 others(15): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77351324 | ||||||
| chr7:77351448
|
T | TAAGAGAA others(307): Show |
5 | a0007c0011t0002g0036a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1491+1495_1491+149 others(318): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77351448 | ||||||
| chr7:77351448
|
T | TAAGAGAA others(308): Show |
1 | a0002c0003t0002g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1491+1495_1491+149 others(319): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77351448 | ||||||
| chr7:77351499
|
T | C | 75 | a0001c0001t0001g0005a0001c0002t0001g0019a0001c0002t0001g0024others(72): Show | 76 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1491+1445A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77351499 | ||||||
| chr7:77351515
|
G | A | 30 | a0004c0005t0001g0106a0004c0005t0001g0107a0004c0005t0001g0172others(27): Show | 30 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1491+1429C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77351515 | ||||||
| chr7:77351566
|
T | C | 1 | a0001c0002t0001g0274 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1491+1378A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77351566 | ||||||
| chr7:77351979
|
G | A | 5 | a0001c0002t0002g0001a0001c0002t0002g0208a0001c0002t0002g0220others(2): Show | 6 | HG01884.hp1 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1491+965C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77351979 | ||||||
| chr7:77352227
|
A | G | 1 | a0001c0002t0001g0264 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1491+717T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77352227 | ||||||
| chr7:77352341
|
C | T | 136 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(133): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1491+603G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77352341 | ||||||
| chr7:77352351
|
T | C | 3 | a0007c0011t0002g0036a0007c0011t0002g0209a0007c0011t0002g0311 | 3 | HG01891.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1491+593A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77352351 | ||||||
| chr7:77352457
|
G | A | 2 | a0002c0003t0001g0089a0002c0003t0001g0090 | 2 | NA18940.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1491+487C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77352457 | ||||||
| chr7:77352792
|
AC | A | 137 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(134): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1491+151delG | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77352792 | ||||||
| chr7:77353101
|
C | G | 16 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0020others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1409-75G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 17/30 | chr7 | 77353101 | ||||||
| chr7:77353163
|
C | T | 137 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(134): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1409-137G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 17/30 | chr7 | 77353163 | ||||||
| chr7:77353231
|
A | G | 1 | a0001c0002t0001g0275 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1409-205T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 17/30 | chr7 | 77353231 | ||||||
| chr7:77353234
|
T | G | 1 | a0001c0001t0001g0074 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1409-208A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 17/30 | chr7 | 77353234 | ||||||
| chr7:77353327
|
A | T | 34 | a0001c0021t0001g0250a0002c0003t0001g0037a0002c0003t0001g0047others(31): Show | 35 | HG00738.hp1 HG01257.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1408+245T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 17/30 | chr7 | 77353327 | ||||||
| chr7:77353351
|
A | G | 1 | a0001c0001t0001g0329 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1408+221T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 17/30 | chr7 | 77353351 | ||||||
| chr7:77353433
|
G | A | 3 | a0003c0009t0001g0189a0003c0009t0001g0190a0003c0009t0001g0192 | 3 | NA18939.hp2 NA18969.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.1408+139C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 17/30 | chr7 | 77353433 | ||||||
| chr7:77353444
|
G | GT | 30 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0046others(27): Show | 31 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.1408+127dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 17/30 | chr7 | 77353444 | ||||||
| chr7:77353496
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1408+76G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 17/30 | chr7 | 77353496 | ||||||
| chr7:77353678
|
A | C | 1 | a0001c0001t0001g0292 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1339-37T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77353678 | ||||||
| chr7:77353820
|
G | A | 1 | a0001c0002t0001g0245 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1339-179C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77353820 | ||||||
| chr7:77353889
|
C | T | 2 | a0001c0002t0001g0262a0001c0002t0001g0299 | 2 | NA18960.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1339-248G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77353889 | ||||||
| chr7:77353905
|
G | A | 1 | a0001c0002t0001g0052 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1339-264C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77353905 | ||||||
| chr7:77353926
|
G | A | 13 | a0002c0003t0001g0287a0002c0003t0001g0312a0002c0003t0001g0313others(10): Show | 13 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1339-285C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77353926 | ||||||
| chr7:77353997
|
A | G | 211 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(208): Show | 213 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1339-356T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77353997 | ||||||
| chr7:77354166
|
T | C | 1 | a0001c0001t0003g0294 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1339-525A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77354166 | ||||||
| chr7:77354198
|
C | T | 45 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(42): Show | 46 | HG00738.hp1 HG01099.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.1339-557G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77354198 | ||||||
| chr7:77354300
|
G | A | 117 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(114): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.1339-659C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77354300 | ||||||
| chr7:77354516
|
A | T | 1 | a0002c0003t0002g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1338+697T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77354516 | ||||||
| chr7:77354677
|
C | CT | 16 | a0001c0002t0001g0283a0001c0002t0002g0008a0001c0002t0002g0009others(13): Show | 16 | HG01433.hp2 HG01891.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1338+535dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77354677 | ||||||
| chr7:77354677
|
C | CTT | 82 | a0001c0002t0001g0019a0001c0002t0001g0024a0001c0002t0001g0052others(79): Show | 83 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1338+534_1338+535d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77354677 | ||||||
| chr7:77354677
|
CT | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(130): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.1338+535delA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77354677 | ||||||
| chr7:77354827
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1338+386C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77354827 | ||||||
| chr7:77354916
|
T | A | 1 | a0001c0002t0002g0208 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1338+297A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77354916 | ||||||
| chr7:77354973
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1338+240C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77354973 | ||||||
| chr7:77355002
|
G | A | 1 | a0012c0022t0001g0130 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1338+211C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77355002 | ||||||
| chr7:77355109
|
T | C | 110 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(107): Show | 112 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1338+104A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77355109 | ||||||
| chr7:77355132
|
C | A | 18 | a0001c0002t0002g0136a0001c0002t0002g0141a0003c0004t0001g0191others(15): Show | 18 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1338+81G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77355132 | ||||||
| chr7:77355149
|
C | T | 5 | a0003c0004t0002g0032a0003c0004t0002g0147a0003c0004t0002g0153others(2): Show | 5 | HG02886.hp2 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1338+64G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77355149 | ||||||
| chr7:77355435
|
C | CA | 48 | a0001c0002t0001g0111a0001c0002t0001g0235a0001c0002t0001g0343others(45): Show | 49 | HG00738.hp1 HG01099.hp1 HG01168.hp2 others(46): Show |
splice_region_variant&intron_variant | LOW | c.1121-6dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 15/30 | chr7 | 77355435 | ||||||
| chr7:77355435
|
CA | C | 124 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(121): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
splice_region_variant&intron_variant | LOW | c.1121-6delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 15/30 | chr7 | 77355435 | ||||||
| chr7:77355714
|
T | C | 2 | a0002c0003t0001g0037a0002c0003t0001g0061 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1028-67A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355714 | ||||||
| chr7:77355787
|
G | GTTTTTTT others(1): Show |
38 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0346others(35): Show | 39 | HG00738.hp1 HG01099.hp1 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.1028-148_1028-141d others(10): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355787 | ||||||
| chr7:77355787
|
G | GTTTTTTT others(2): Show |
48 | a0001c0002t0001g0345a0001c0002t0002g0136a0001c0002t0002g0141others(45): Show | 49 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.1028-149_1028-141d others(11): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355787 | ||||||
| chr7:77355787
|
G | GTTTTTTT others(3): Show |
16 | a0002c0003t0001g0020a0002c0003t0001g0102a0002c0003t0001g0312others(13): Show | 16 | HG00639.hp1 HG00642.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1028-150_1028-141d others(12): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355787 | ||||||
| chr7:77355787
|
G | GTTTTTTT others(4): Show |
8 | a0002c0003t0001g0018a0002c0003t0001g0287a0002c0003t0001g0336others(5): Show | 8 | HG01109.hp2 HG01243.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.1028-151_1028-141d others(13): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355787 | ||||||
| chr7:77355787
|
GT | G | 179 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(176): Show | 181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1028-141delA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355787 | ||||||
| chr7:77355787
|
GTT | G | 14 | a0001c0001t0001g0030a0001c0001t0001g0261a0001c0002t0001g0276others(11): Show | 14 | HG00423.hp2 HG01167.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.1028-142_1028-141d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355787 | ||||||
| chr7:77355807
|
A | T | 110 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(107): Show | 112 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1028-160T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355807 | ||||||
| chr7:77355878
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1028-231G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355878 | ||||||
| chr7:77355971
|
T | C | 23 | a0001c0002t0002g0136a0001c0002t0002g0141a0003c0004t0001g0191others(20): Show | 23 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1028-324A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355971 | ||||||
| chr7:77355995
|
T | C | 1 | a0001c0002t0001g0242 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1028-348A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355995 | ||||||
| chr7:77356024
|
TCAAG | T | 110 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(107): Show | 112 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1028-381_1028-378d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356024 | ||||||
| chr7:77356027
|
A | G | 1 | a0001c0002t0001g0144 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1028-380T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356027 | ||||||
| chr7:77356174
|
A | G | 9 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(6): Show | 9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1028-527T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356174 | ||||||
| chr7:77356353
|
C | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0084 | 2 | HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1028-706G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356353 | ||||||
| chr7:77356464
|
TATC | T | 9 | a0002c0007t0001g0003a0002c0007t0001g0228a0002c0007t0001g0229others(6): Show | 10 | NA18946.hp2 NA18978.hp2 NA18981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1028-820_1028-818d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356464 | ||||||
| chr7:77356533
|
G | A | 4 | a0001c0002t0001g0233a0001c0002t0001g0234a0001c0002t0001g0241others(1): Show | 4 | NA18952.hp1 NA18982.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1028-886C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356533 | ||||||
| chr7:77356563
|
A | T | 4 | a0001c0002t0001g0158a0001c0002t0001g0240a0001c0002t0001g0262others(1): Show | 4 | HG00544.hp2 HG00558.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.1028-916T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356563 | ||||||
| chr7:77356603
|
T | C | 3 | a0006c0008t0001g0016a0006c0008t0001g0137a0009c0026t0001g0053 | 3 | HG01074.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1028-956A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356603 | ||||||
| chr7:77356641
|
TTG | T | 27 | a0002c0003t0001g0047a0002c0003t0001g0057a0002c0003t0001g0058others(24): Show | 28 | HG00738.hp1 HG01257.hp2 HG02273.hp2 others(25): Show |
intron_variant | MODIFIER | c.1028-996_1028-995d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356641 | ||||||
| chr7:77356713
|
A | G | 1 | a0004c0005t0003g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1028-1066T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356713 | ||||||
| chr7:77356874
|
G | T | 1 | a0006c0008t0001g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1028-1227C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356874 | ||||||
| chr7:77356997
|
C | A | 110 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(107): Show | 112 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1028-1350G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356997 | ||||||
| chr7:77357343
|
A | G | 1 | a0002c0003t0001g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1028-1696T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77357343 | ||||||
| chr7:77357493
|
C | T | 106 | a0001c0002t0002g0136a0001c0002t0002g0141a0002c0003t0001g0004others(103): Show | 108 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1028-1846G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77357493 | ||||||
| chr7:77357501
|
C | T | 6 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1028-1854G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77357501 | ||||||
| chr7:77357534
|
G | A | 1 | a0003c0004t0002g0153 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1028-1887C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77357534 | ||||||
| chr7:77357569
|
GGAA | G | 5 | a0002c0003t0002g0054a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1028-1925_1028-192 others(7): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77357569 | ||||||
| chr7:77357663
|
A | G | 1 | a0001c0002t0002g0141 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1028-2016T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77357663 | ||||||
| chr7:77357737
|
TGGAG | T | 5 | a0002c0003t0002g0054a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1028-2094_1028-209 others(8): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77357737 | ||||||
| chr7:77357812
|
G | A | 47 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(44): Show | 48 | HG00738.hp1 HG01099.hp1 HG01168.hp2 others(45): Show |
intron_variant | MODIFIER | c.1028-2165C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77357812 | ||||||
| chr7:77358105
|
C | T | 1 | a0002c0003t0001g0225 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1028-2458G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77358105 | ||||||
| chr7:77358161
|
C | A | 3 | a0001c0010t0001g0146a0001c0010t0001g0150a0001c0010t0001g0152 | 3 | HG03139.hp2 HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1028-2514G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77358161 | ||||||
| chr7:77358162
|
A | G | 64 | a0001c0002t0002g0136a0001c0002t0002g0141a0002c0003t0001g0004others(61): Show | 65 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.1028-2515T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77358162 | ||||||
| chr7:77358186
|
T | C | 129 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0031others(126): Show | 132 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1028-2539A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77358186 | ||||||
| chr7:77358203
|
A | C | 1 | a0003c0004t0002g0185 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1028-2556T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77358203 | ||||||
| chr7:77358366
|
G | A | 105 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(102): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1027+2458C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77358366 | ||||||
| chr7:77358367
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1027+2457C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77358367 | ||||||
| chr7:77358840
|
A | G | 110 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(107): Show | 112 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1027+1984T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77358840 | ||||||
| chr7:77359015
|
C | T | 110 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(107): Show | 112 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1027+1809G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77359015 | ||||||
| chr7:77359059
|
C | T | 5 | a0002c0003t0001g0037a0002c0003t0001g0061a0002c0003t0001g0062others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1027+1765G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77359059 | ||||||
| chr7:77359060
|
G | A | 2 | a0001c0001t0001g0332a0002c0003t0001g0004 | 3 | HG00280.hp2 HG00323.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1027+1764C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77359060 | ||||||
| chr7:77359126
|
C | G | 110 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(107): Show | 112 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1027+1698G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77359126 | ||||||
| chr7:77359142
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1027+1682T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77359142 | ||||||
| chr7:77359200
|
C | CA | 56 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(53): Show | 57 | HG00738.hp1 HG01099.hp1 HG01168.hp2 others(54): Show |
intron_variant | MODIFIER | c.1027+1623dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77359200 | ||||||
| chr7:77359207
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1027+1617T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77359207 | ||||||
| chr7:77359209
|
A | G | 18 | a0001c0002t0002g0136a0001c0002t0002g0141a0003c0004t0001g0191others(15): Show | 18 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1027+1615T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77359209 | ||||||
| chr7:77359241
|
A | G | 1 | a0001c0002t0001g0144 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1027+1583T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77359241 | ||||||
| chr7:77359706
|
A | G | 112 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(109): Show | 114 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.1027+1118T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77359706 | ||||||
| chr7:77360065
|
T | C | 1 | a0001c0001t0001g0290 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1027+759A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77360065 | ||||||
| chr7:77360075
|
T | C | 110 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(107): Show | 112 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1027+749A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77360075 | ||||||
| chr7:77360129
|
T | A | 5 | a0003c0004t0002g0032a0003c0004t0002g0147a0003c0004t0002g0153others(2): Show | 5 | HG02886.hp2 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1027+695A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77360129 | ||||||
| chr7:77360336
|
G | A | 2 | a0001c0002t0002g0120a0001c0002t0002g0183 | 2 | HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1027+488C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77360336 | ||||||
| chr7:77360719
|
C | T | 6 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1027+105G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77360719 | ||||||
| chr7:77360764
|
G | A | 1 | a0001c0002t0001g0118 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1027+60C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77360764 | ||||||
| chr7:77360809
|
C | T | 104 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0020others(101): Show | 106 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1027+15G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77360809 | ||||||
| chr7:77361055
|
C | A | 80 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(77): Show | 81 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.950-154G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77361055 | ||||||
| chr7:77361197
|
A | C | 1 | a0001c0002t0001g0276 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.950-296T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77361197 | ||||||
| chr7:77361209
|
A | G | 2 | a0001c0002t0002g0108a0001c0002t0002g0109 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.950-308T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77361209 | ||||||
| chr7:77361566
|
T | C | 1 | a0012c0022t0001g0130 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.950-665A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77361566 | ||||||
| chr7:77361618
|
G | A | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.950-717C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77361618 | ||||||
| chr7:77361648
|
C | A | 1 | a0002c0003t0001g0347 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.950-747G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77361648 | ||||||
| chr7:77361682
|
T | C | 111 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(108): Show | 113 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.950-781A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77361682 | ||||||
| chr7:77361794
|
G | A | 2 | a0001c0002t0001g0158a0001c0002t0001g0240 | 2 | HG00544.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.949+789C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77361794 | ||||||
| chr7:77361832
|
T | C | 316 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(313): Show | 320 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.949+751A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77361832 | ||||||
| chr7:77362153
|
T | C | 108 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(105): Show | 110 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.949+430A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77362153 | ||||||
| chr7:77362257
|
C | T | 1 | a0002c0003t0001g0121 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.949+326G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77362257 | ||||||
| chr7:77362453
|
T | G | 1 | a0002c0003t0001g0148 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.949+130A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77362453 | ||||||
| chr7:77362458
|
G | C | 1 | a0002c0003t0003g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.949+125C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77362458 | ||||||
| chr7:77362506
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.949+77G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77362506 | ||||||
| chr7:77362696
|
A | G | 10 | a0002c0018t0001g0100a0003c0004t0002g0114a0003c0004t0002g0124others(7): Show | 10 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.872-36T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77362696 | ||||||
| chr7:77362932
|
G | A | 1 | a0001c0002t0001g0274 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.872-272C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77362932 | ||||||
| chr7:77362961
|
A | G | 109 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(106): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.872-301T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77362961 | ||||||
| chr7:77363038
|
C | T | 1 | a0002c0027t0001g0215 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.872-378G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77363038 | ||||||
| chr7:77363305
|
C | T | 104 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0020others(101): Show | 106 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.872-645G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77363305 | ||||||
| chr7:77363597
|
G | A | 1 | a0001c0002t0001g0285 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.872-937C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77363597 | ||||||
| chr7:77363867
|
T | C | 316 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(313): Show | 320 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.872-1207A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77363867 | ||||||
| chr7:77363915
|
AATAATT | A | 3 | a0001c0002t0001g0268a0001c0002t0001g0272a0001c0002t0001g0273 | 3 | HG01069.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.872-1261_872-1256d others(8): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77363915 | ||||||
| chr7:77364260
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(109): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.872-1600G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77364260 | ||||||
| chr7:77364335
|
C | T | 1 | a0002c0003t0001g0121 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.872-1675G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77364335 | ||||||
| chr7:77364461
|
A | G | 110 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(107): Show | 112 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.872-1801T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77364461 | ||||||
| chr7:77364478
|
C | A | 13 | a0002c0003t0001g0287a0002c0003t0001g0312a0002c0003t0001g0313others(10): Show | 13 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.872-1818G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77364478 | ||||||
| chr7:77364534
|
A | G | 1 | a0001c0002t0001g0110 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.872-1874T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77364534 | ||||||
| chr7:77364668
|
G | A | 108 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(105): Show | 110 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.872-2008C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77364668 | ||||||
| chr7:77364672
|
TAATAA | T | 3 | a0003c0004t0002g0341a0003c0004t0002g0342a0005c0006t0001g0173 | 3 | HG00642.hp1 HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.872-2017_872-2013d others(7): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77364672 | ||||||
| chr7:77364736
|
A | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0069 | 2 | HG00639.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.872-2076T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77364736 | ||||||
| chr7:77364930
|
T | C | 10 | a0004c0005t0001g0172a0004c0005t0003g0160a0004c0005t0003g0161others(7): Show | 10 | HG00558.hp2 HG00621.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.872-2270A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77364930 | ||||||
| chr7:77364933
|
C | T | 100 | a0001c0002t0002g0136a0001c0002t0002g0141a0002c0003t0001g0004others(97): Show | 102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.872-2273G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77364933 | ||||||
| chr7:77365111
|
T | A | 7 | a0002c0003t0001g0287a0002c0003t0001g0312a0002c0003t0001g0313others(4): Show | 7 | HG01074.hp1 HG01109.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.872-2451A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365111 | ||||||
| chr7:77365144
|
G | A | 1 | a0005c0006t0001g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.872-2484C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365144 | ||||||
| chr7:77365172
|
TC | T | 100 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0020others(97): Show | 102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.872-2513delG | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365172 | ||||||
| chr7:77365244
|
T | A | 17 | a0001c0001t0001g0205a0002c0003t0001g0004a0002c0003t0001g0018others(14): Show | 18 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.872-2584A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365244 | ||||||
| chr7:77365304
|
G | A | 2 | a0001c0002t0002g0136a0001c0002t0002g0141 | 2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.872-2644C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365304 | ||||||
| chr7:77365445
|
A | G | 62 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(59): Show | 63 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(60): Show |
intron_variant | MODIFIER | c.872-2785T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365445 | ||||||
| chr7:77365716
|
T | C | 10 | a0002c0027t0001g0215a0006c0008t0001g0016a0006c0008t0001g0051others(7): Show | 10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.872-3056A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365716 | ||||||
| chr7:77365834
|
C | T | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.872-3174G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365834 | ||||||
| chr7:77365898
|
G | GT | 28 | a0001c0001t0001g0022a0001c0001t0001g0069a0001c0001t0001g0261others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.872-3239dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365898 | ||||||
| chr7:77365898
|
GT | G | 124 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0031others(121): Show | 126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.872-3239delA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365898 | ||||||
| chr7:77365908
|
T | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0210a0001c0001t0001g0251others(49): Show | 54 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.872-3248A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365908 | ||||||
| chr7:77365953
|
G | A | 5 | a0001c0001t0001g0295a0001c0001t0001g0314a0001c0001t0001g0315others(2): Show | 5 | NA18939.hp1 NA18946.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.872-3293C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365953 | ||||||
| chr7:77365962
|
T | C | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.872-3302A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365962 | ||||||
| chr7:77366149
|
G | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(113): Show | 117 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.872-3489C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77366149 | ||||||
| chr7:77366262
|
GCTT | G | 4 | a0007c0011t0002g0139a0007c0011t0002g0145a0007c0011t0002g0209others(1): Show | 4 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.872-3605_872-3603d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77366262 | ||||||
| chr7:77366320
|
C | T | 1 | a0003c0009t0001g0190 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.872-3660G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77366320 | ||||||
| chr7:77366323
|
G | A | 1 | a0007c0011t0002g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.872-3663C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77366323 | ||||||
| chr7:77366835
|
A | G | 80 | a0001c0001t0001g0002a0001c0001t0001g0210a0001c0001t0001g0251others(77): Show | 82 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.872-4175T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77366835 | ||||||
| chr7:77367037
|
G | C | 78 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(75): Show | 79 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.872-4377C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77367037 | ||||||
| chr7:77367158
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.872-4498C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77367158 | ||||||
| chr7:77367172
|
A | T | 1 | a0009c0026t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.872-4512T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77367172 | ||||||
| chr7:77367207
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.872-4547G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77367207 | ||||||
| chr7:77367276
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.872-4616A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77367276 | ||||||
| chr7:77367314
|
T | G | 17 | a0001c0001t0001g0205a0002c0003t0001g0004a0002c0003t0001g0018others(14): Show | 18 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.872-4654A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77367314 | ||||||
| chr7:77367755
|
G | C | 1 | a0006c0008t0001g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.872-5095C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77367755 | ||||||
| chr7:77367795
|
C | T | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.872-5135G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77367795 | ||||||
| chr7:77367875
|
G | C | 1 | a0006c0008t0001g0142 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.872-5215C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77367875 | ||||||
| chr7:77367948
|
G | A | 2 | a0001c0002t0001g0019a0001c0002t0001g0024 | 2 | NA18940.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.872-5288C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77367948 | ||||||
| chr7:77368250
|
C | T | 1 | a0001c0002t0002g0128 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.872-5590G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77368250 | ||||||
| chr7:77368384
|
C | A | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871+5686G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77368384 | ||||||
| chr7:77368608
|
A | G | 2 | a0004c0005t0003g0159a0004c0005t0003g0162 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.871+5462T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77368608 | ||||||
| chr7:77368645
|
G | T | 5 | a0002c0003t0002g0054a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.871+5425C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77368645 | ||||||
| chr7:77368649
|
G | A | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871+5421C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77368649 | ||||||
| chr7:77368738
|
T | C | 49 | a0001c0001t0001g0291a0001c0002t0001g0343a0001c0002t0001g0344others(46): Show | 50 | HG00738.hp1 HG01099.hp1 HG01168.hp2 others(47): Show |
intron_variant | MODIFIER | c.871+5332A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77368738 | ||||||
| chr7:77368746
|
T | C | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871+5324A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77368746 | ||||||
| chr7:77368927
|
G | C | 1 | a0002c0003t0001g0347 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.871+5143C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77368927 | ||||||
| chr7:77368953
|
G | A | 6 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.871+5117C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77368953 | ||||||
| chr7:77368969
|
C | T | 55 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(52): Show | 55 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.871+5101G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77368969 | ||||||
| chr7:77369194
|
A | G | 1 | a0001c0002t0006g0006 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.871+4876T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369194 | ||||||
| chr7:77369225
|
G | C | 17 | a0001c0001t0001g0205a0002c0003t0001g0004a0002c0003t0001g0018others(14): Show | 18 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.871+4845C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369225 | ||||||
| chr7:77369266
|
G | A | 1 | a0001c0021t0001g0250 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.871+4804C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369266 | ||||||
| chr7:77369591
|
T | C | 1 | a0001c0023t0001g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.871+4479A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369591 | ||||||
| chr7:77369605
|
G | A | 131 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0205others(128): Show | 134 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.871+4465C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369605 | ||||||
| chr7:77369740
|
C | T | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871+4330G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369740 | ||||||
| chr7:77369782
|
T | TA | 23 | a0001c0001t0001g0007a0002c0018t0001g0100a0003c0004t0001g0191others(20): Show | 23 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.871+4287dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369782 | ||||||
| chr7:77369803
|
T | G | 1 | a0001c0002t0001g0302 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.871+4267A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369803 | ||||||
| chr7:77369901
|
C | CTTTTT | 9 | a0002c0007t0001g0003a0002c0007t0001g0228a0002c0007t0001g0229others(6): Show | 10 | NA18946.hp2 NA18978.hp2 NA18981.hp1 others(7): Show |
intron_variant | MODIFIER | c.871+4168_871+4169i others(7): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369901 | ||||||
| chr7:77369902
|
G | GTTTTT | 121 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0205others(118): Show | 123 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.871+4163_871+4167d others(7): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369902 | ||||||
| chr7:77369902
|
G | T | 9 | a0002c0007t0001g0003a0002c0007t0001g0228a0002c0007t0001g0229others(6): Show | 10 | NA18946.hp2 NA18978.hp2 NA18981.hp1 others(7): Show |
intron_variant | MODIFIER | c.871+4168C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369902 | ||||||
| chr7:77369986
|
A | G | 17 | a0001c0001t0001g0205a0002c0003t0001g0004a0002c0003t0001g0018others(14): Show | 18 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.871+4084T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369986 | ||||||
| chr7:77370255
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.871+3815G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77370255 | ||||||
| chr7:77370260
|
C | T | 1 | a0001c0002t0001g0282 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.871+3810G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77370260 | ||||||
| chr7:77370265
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.871+3805C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77370265 | ||||||
| chr7:77370286
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.871+3784G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77370286 | ||||||
| chr7:77370422
|
T | C | 3 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0112 | 3 | NA18945.hp1 NA19003.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.871+3648A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77370422 | ||||||
| chr7:77370840
|
A | AC | 11 | a0001c0028t0002g0143a0002c0027t0001g0215a0006c0008t0001g0016others(8): Show | 11 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.871+3229dupG | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77370840 | ||||||
| chr7:77370967
|
A | G | 9 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(6): Show | 9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.871+3103T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77370967 | ||||||
| chr7:77371085
|
G | C | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871+2985C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371085 | ||||||
| chr7:77371099
|
C | CA | 3 | a0001c0002t0002g0120a0001c0002t0002g0183a0001c0002t0004g0033 | 3 | HG01243.hp1 HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.871+2970dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371099 | ||||||
| chr7:77371415
|
G | A | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871+2655C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371415 | ||||||
| chr7:77371431
|
CT | C | 36 | a0001c0001t0001g0205a0001c0001t0001g0296a0001c0001t0001g0297others(33): Show | 37 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.871+2638delA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371431 | ||||||
| chr7:77371431
|
CTT | C | 83 | a0001c0001t0001g0196a0001c0001t0001g0203a0001c0002t0001g0019others(80): Show | 84 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.871+2637_871+2638d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371431 | ||||||
| chr7:77371431
|
CTTT | C | 194 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(191): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.871+2636_871+2638d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371431 | ||||||
| chr7:77371434
|
T | C | 1 | a0001c0002t0001g0304 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.871+2636A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371434 | ||||||
| chr7:77371437
|
T | C | 2 | a0001c0002t0002g0136a0001c0002t0002g0141 | 2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.871+2633A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371437 | ||||||
| chr7:77371439
|
T | C | 16 | a0001c0001t0001g0196a0001c0001t0001g0203a0001c0028t0002g0143others(13): Show | 16 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.871+2631A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371439 | ||||||
| chr7:77371440
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(180): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.871+2630A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371440 | ||||||
| chr7:77371441
|
T | C | 1 | a0002c0003t0001g0122 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.871+2629A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371441 | ||||||
| chr7:77371450
|
T | C | 22 | a0002c0018t0001g0100a0003c0004t0001g0191a0003c0004t0002g0032others(19): Show | 22 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.871+2620A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371450 | ||||||
| chr7:77371520
|
C | T | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871+2550G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371520 | ||||||
| chr7:77371665
|
G | A | 3 | a0001c0002t0001g0271a0001c0002t0001g0301a0001c0002t0001g0318 | 3 | NA18988.hp1 NA19001.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.871+2405C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371665 | ||||||
| chr7:77371717
|
G | A | 105 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0014others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.871+2353C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371717 | ||||||
| chr7:77371726
|
C | T | 1 | a0001c0002t0002g0011 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.871+2344G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371726 | ||||||
| chr7:77371808
|
A | G | 1 | a0001c0002t0001g0308 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.871+2262T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371808 | ||||||
| chr7:77371811
|
C | T | 1 | a0001c0002t0001g0279 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.871+2259G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371811 | ||||||
| chr7:77371884
|
G | A | 106 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0014others(103): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.871+2186C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371884 | ||||||
| chr7:77371895
|
A | G | 2 | a0001c0002t0002g0120a0001c0002t0002g0183 | 2 | HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.871+2175T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371895 | ||||||
| chr7:77371937
|
A | G | 4 | a0001c0002t0001g0233a0001c0002t0001g0234a0001c0002t0001g0241others(1): Show | 4 | NA18952.hp1 NA18982.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.871+2133T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371937 | ||||||
| chr7:77372001
|
T | TA | 5 | a0001c0028t0002g0143a0006c0008t0001g0135a0006c0008t0001g0138others(2): Show | 5 | HG00639.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.871+2068dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77372001 | ||||||
| chr7:77372069
|
C | T | 1 | a0001c0002t0001g0240 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.871+2001G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77372069 | ||||||
| chr7:77372146
|
A | G | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871+1924T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77372146 | ||||||
| chr7:77372320
|
G | A | 1 | a0004c0005t0003g0178 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.871+1750C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77372320 | ||||||
| chr7:77372334
|
T | C | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871+1736A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77372334 | ||||||
| chr7:77372378
|
A | C | 4 | a0007c0011t0002g0139a0007c0011t0002g0145a0007c0011t0002g0209others(1): Show | 4 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.871+1692T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77372378 | ||||||
| chr7:77372511
|
A | C | 1 | a0003c0004t0002g0157 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.871+1559T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77372511 | ||||||
| chr7:77372826
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0022 | 2 | NA18960.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.871+1244C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77372826 | ||||||
| chr7:77372843
|
C | T | 1 | a0006c0008t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.871+1227G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77372843 | ||||||
| chr7:77372991
|
C | T | 9 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(6): Show | 9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.871+1079G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77372991 | ||||||
| chr7:77373238
|
A | G | 6 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.871+832T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77373238 | ||||||
| chr7:77373461
|
C | T | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871+609G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77373461 | ||||||
| chr7:77373484
|
G | T | 9 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(6): Show | 9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.871+586C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77373484 | ||||||
| chr7:77373580
|
G | A | 1 | a0001c0002t0001g0300 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.871+490C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77373580 | ||||||
| chr7:77373960
|
A | G | 10 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(7): Show | 10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.871+110T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77373960 | ||||||
| chr7:77374022
|
A | C | 1 | a0001c0002t0001g0276 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.871+48T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77374022 | ||||||
| chr7:77374285
|
A | C | 10 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(7): Show | 10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.786-130T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 11/30 | chr7 | 77374285 | ||||||
| chr7:77374485
|
C | T | 5 | a0002c0003t0002g0054a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.786-330G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 11/30 | chr7 | 77374485 | ||||||
| chr7:77374602
|
G | A | 1 | a0001c0002t0004g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.786-447C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 11/30 | chr7 | 77374602 | ||||||
| chr7:77374646
|
GA | G | 9 | a0001c0002t0001g0270a0001c0028t0002g0143a0002c0027t0001g0215others(6): Show | 9 | HG00639.hp1 HG01109.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.785+411delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 11/30 | chr7 | 77374646 | ||||||
| chr7:77374660
|
C | A | 3 | a0001c0001t0001g0256a0003c0004t0001g0191a0014c0017t0001g0348 | 3 | HG02523.hp2 NA18978.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.785+398G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 11/30 | chr7 | 77374660 | ||||||
| chr7:77374919
|
T | G | 1 | a0002c0003t0002g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.785+139A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 11/30 | chr7 | 77374919 | ||||||
| chr7:77374992
|
G | A | 5 | a0002c0003t0002g0054a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.785+66C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 11/30 | chr7 | 77374992 | ||||||
| chr7:77375026
|
T | C | 4 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(1): Show | 4 | HG01099.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.785+32A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 11/30 | chr7 | 77375026 | ||||||
| chr7:77375045
|
A | C | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.785+13T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 11/30 | chr7 | 77375045 | ||||||
| chr7:77375199
|
T | C | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.742-98A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375199 | ||||||
| chr7:77375369
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.742-268T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375369 | ||||||
| chr7:77375380
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.742-279T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375380 | ||||||
| chr7:77375451
|
A | C | 81 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(78): Show | 82 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.742-350T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375451 | ||||||
| chr7:77375486
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.742-385T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375486 | ||||||
| chr7:77375574
|
G | T | 49 | a0002c0003t0001g0037a0002c0003t0001g0047a0002c0003t0001g0057others(46): Show | 50 | HG00738.hp1 HG01257.hp2 HG01884.hp2 others(47): Show |
intron_variant | MODIFIER | c.742-473C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375574 | ||||||
| chr7:77375739
|
G | A | 1 | a0002c0003t0001g0122 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.742-638C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375739 | ||||||
| chr7:77375810
|
C | T | 70 | a0002c0003t0001g0037a0002c0003t0001g0047a0002c0003t0001g0057others(67): Show | 71 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.742-709G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375810 | ||||||
| chr7:77375843
|
TA | T | 285 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(282): Show | 288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.742-743delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375843 | ||||||
| chr7:77375855
|
A | C | 3 | a0001c0001t0001g0195a0004c0005t0003g0105a0005c0006t0001g0207 | 3 | HG04184.hp2 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.742-754T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375855 | ||||||
| chr7:77375858
|
AC | A | 5 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(2): Show | 5 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.742-758delG | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375858 | ||||||
| chr7:77375859
|
C | A | 2 | a0003c0004t0005g0186a0014c0017t0001g0348 | 2 | HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.742-758G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375859 | ||||||
| chr7:77376064
|
C | T | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.741+784G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376064 | ||||||
| chr7:77376310
|
T | C | 317 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(314): Show | 321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.741+538A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376310 | ||||||
| chr7:77376380
|
A | G | 304 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(301): Show | 308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.741+468T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376380 | ||||||
| chr7:77376417
|
C | T | 6 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.741+431G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376417 | ||||||
| chr7:77376511
|
C | T | 6 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.741+337G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376511 | ||||||
| chr7:77376518
|
G | A | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.741+330C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376518 | ||||||
| chr7:77376620
|
A | C | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.741+228T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376620 | ||||||
| chr7:77376646
|
G | A | 1 | a0002c0003t0001g0047 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.741+202C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376646 | ||||||
| chr7:77376651
|
C | A | 79 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(76): Show | 80 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.741+197G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376651 | ||||||
| chr7:77376663
|
G | C | 1 | a0004c0005t0001g0107 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.741+185C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376663 | ||||||
| chr7:77376748
|
CGTGTGCG others(5): Show |
C | 1 | a0001c0001t0001g0327 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.741+88_741+99delTC others(10): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376748 | ||||||
| chr7:77376767
|
C | A | 1 | a0004c0005t0003g0289 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.741+81G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376767 | ||||||
| chr7:77376775
|
C | CA | 8 | a0001c0001t0001g0017a0001c0001t0001g0084a0004c0005t0003g0159others(5): Show | 8 | HG01074.hp1 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.741+72dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376775 | ||||||
| chr7:77376775
|
C | CAA | 10 | a0001c0028t0002g0143a0002c0027t0001g0215a0006c0008t0001g0101others(7): Show | 10 | HG00639.hp1 HG01109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.741+71_741+72dupTT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376775 | ||||||
| chr7:77376775
|
C | CAAA | 7 | a0002c0003t0002g0054a0003c0004t0002g0032a0003c0004t0002g0147others(4): Show | 7 | HG02622.hp1 HG02886.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.741+70_741+72dupTT others(1): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376775 | ||||||
| chr7:77376775
|
CA | C | 83 | a0001c0001t0001g0040a0001c0001t0001g0113a0001c0001t0001g0210others(80): Show | 85 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.741+72delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376775 | ||||||
| chr7:77376775
|
CAAAAAA | C | 11 | a0001c0002t0002g0001a0001c0002t0002g0120a0001c0002t0002g0126others(8): Show | 12 | HG01192.hp2 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.741+67_741+72delTT others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376775 | ||||||
| chr7:77376788
|
AAAAAAAA others(1): Show |
A | 66 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.741+52_741+59delCT others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376788 | ||||||
| chr7:77376797
|
A | G | 16 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0020others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.741+51T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376797 | ||||||
| chr7:77376922
|
A | G | 1 | a0001c0002t0001g0275 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.682-15T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77376922 | ||||||
| chr7:77377217
|
T | TA | 16 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0020others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.681+68dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377217 | ||||||
| chr7:77377237
|
T | TA | 125 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(122): Show | 127 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.681+48dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | ||||||
| chr7:77377237
|
T | TAA | 22 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0050others(19): Show | 22 | HG00099.hp2 HG00735.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.681+47_681+48dupTT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | ||||||
| chr7:77377237
|
T | TAAAAAAA | 24 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(21): Show | 25 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.681+42_681+48dupTT others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | ||||||
| chr7:77377237
|
T | TAAAAAAA others(4): Show |
1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.681+38_681+48dupTT others(9): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | ||||||
| chr7:77377237
|
T | TAAAAAAA others(6): Show |
3 | a0003c0004t0002g0184a0003c0004t0002g0185a0003c0004t0002g0188 | 3 | HG02965.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.681+36_681+48dupTT others(11): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | ||||||
| chr7:77377237
|
T | TAAAAAAA others(7): Show |
3 | a0003c0004t0002g0133a0003c0004t0002g0187a0003c0004t0005g0186 | 3 | HG01891.hp1 HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.681+35_681+48dupTT others(12): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | ||||||
| chr7:77377237
|
T | TAAAAAAA others(8): Show |
1 | a0002c0003t0001g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.681+34_681+48dupTT others(13): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | ||||||
| chr7:77377237
|
T | TAAAAAAA others(9): Show |
7 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0346others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.681+33_681+48dupTT others(14): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | ||||||
| chr7:77377237
|
T | TAAAAAAA others(10): Show |
23 | a0001c0002t0001g0345a0002c0003t0001g0057a0002c0003t0001g0058others(20): Show | 23 | HG00140.hp1 HG00738.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.681+32_681+48dupTT others(15): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | ||||||
| chr7:77377237
|
T | TAAAAAAA others(11): Show |
17 | a0002c0003t0001g0062a0002c0003t0001g0063a0002c0003t0001g0065others(14): Show | 17 | HG01258.hp1 HG01516.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.681+31_681+48dupTT others(16): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | ||||||
| chr7:77377237
|
T | TAAAAAAA others(12): Show |
8 | a0002c0003t0001g0068a0002c0003t0001g0090a0002c0003t0001g0320others(5): Show | 8 | HG00642.hp1 HG01106.hp1 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.681+30_681+48dupTT others(17): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | ||||||
| chr7:77377237
|
T | TAAAAAAA others(13): Show |
4 | a0002c0007t0001g0003a0002c0007t0001g0228a0002c0007t0001g0325others(1): Show | 5 | NA18978.hp2 NA19062.hp2 NA19085.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+29_681+48dupTT others(18): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | ||||||
| chr7:77377237
|
T | TAAAAAAA others(14): Show |
1 | a0002c0003t0001g0047 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.681+28_681+48dupTT others(19): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | ||||||
| chr7:77377237
|
T | TAAAAAAA others(19): Show |
1 | a0002c0003t0001g0061 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.681+48_681+49insTT others(24): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | ||||||
| chr7:77377237
|
T | TAAAAAAA others(21): Show |
1 | a0002c0003t0001g0037 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.681+48_681+49insTT others(26): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | ||||||
| chr7:77377268
|
G | A | 2 | a0006c0008t0001g0135a0006c0008t0001g0142 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.681+18C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377268 | ||||||
| chr7:77377400
|
C | CA | 74 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(71): Show | 75 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.577-11dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377400 | ||||||
| chr7:77377400
|
C | CAA | 13 | a0001c0002t0001g0118a0001c0002t0001g0144a0001c0002t0001g0233others(10): Show | 13 | HG00597.hp1 HG01099.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.577-12_577-11dupTT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377400 | ||||||
| chr7:77377400
|
CA | C | 18 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0081others(15): Show | 18 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.577-11delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377400 | ||||||
| chr7:77377400
|
CAA | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.577-12_577-11delTT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377400 | ||||||
| chr7:77377400
|
CAAA | C | 72 | a0001c0001t0001g0293a0001c0001t0001g0295a0001c0002t0001g0343others(69): Show | 73 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.577-13_577-11delTT others(1): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377400 | ||||||
| chr7:77377400
|
CAAAA | C | 10 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(7): Show | 10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.577-14_577-11delTT others(2): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377400 | ||||||
| chr7:77377400
|
CAAAAAA | C | 17 | a0001c0001t0001g0335a0002c0003t0001g0004a0002c0003t0001g0018others(14): Show | 18 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.577-16_577-11delTT others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377400 | ||||||
| chr7:77377609
|
A | G | 16 | a0003c0004t0001g0191a0003c0004t0002g0114a0003c0004t0002g0124others(13): Show | 16 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.577-219T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377609 | ||||||
| chr7:77377850
|
A | G | 1 | a0002c0003t0001g0058 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.577-460T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377850 | ||||||
| chr7:77377880
|
T | G | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.577-490A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377880 | ||||||
| chr7:77377937
|
C | G | 1 | a0012c0022t0001g0130 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.577-547G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377937 | ||||||
| chr7:77378327
|
T | A | 1 | a0001c0001t0001g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.577-937A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378327 | ||||||
| chr7:77378430
|
G | A | 2 | a0002c0003t0001g0089a0002c0003t0001g0090 | 2 | NA18940.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.577-1040C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378430 | ||||||
| chr7:77378433
|
A | G | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.577-1043T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378433 | ||||||
| chr7:77378436
|
A | T | 4 | a0007c0011t0002g0139a0007c0011t0002g0145a0007c0011t0002g0209others(1): Show | 4 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-1046T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378436 | ||||||
| chr7:77378461
|
G | A | 1 | a0002c0003t0001g0320 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.577-1071C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378461 | ||||||
| chr7:77378465
|
C | T | 6 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.577-1075G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378465 | ||||||
| chr7:77378520
|
C | CA | 6 | a0001c0001t0001g0041a0001c0002t0001g0284a0001c0002t0002g0136others(3): Show | 6 | HG01099.hp2 HG01255.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.577-1131dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378520 | ||||||
| chr7:77378520
|
C | CAA | 10 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(7): Show | 10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.577-1132_577-1131d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378520 | ||||||
| chr7:77378523
|
A | C | 26 | a0002c0003t0001g0058a0002c0003t0001g0065a0002c0003t0001g0066others(23): Show | 26 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.577-1133T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378523 | ||||||
| chr7:77378526
|
A | C | 1 | a0003c0004t0002g0114 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.577-1136T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378526 | ||||||
| chr7:77378527
|
AAAC | A | 5 | a0002c0003t0002g0054a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.577-1140_577-1138d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378527 | ||||||
| chr7:77378529
|
AC | A | 9 | a0002c0003t0001g0057a0002c0003t0001g0064a0002c0003t0001g0068others(6): Show | 9 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.577-1140delG | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378529 | ||||||
| chr7:77378530
|
C | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0210a0001c0001t0001g0251others(60): Show | 65 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.577-1140G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378530 | ||||||
| chr7:77378680
|
A | C | 7 | a0001c0001t0001g0044a0001c0001t0001g0077a0001c0001t0001g0193others(4): Show | 7 | HG00544.hp1 NA18983.hp1 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.577-1290T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378680 | ||||||
| chr7:77378953
|
G | A | 3 | a0001c0002t0001g0271a0001c0002t0001g0301a0001c0002t0001g0318 | 3 | NA18988.hp1 NA19001.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.577-1563C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378953 | ||||||
| chr7:77379149
|
A | G | 2 | a0001c0002t0002g0136a0001c0002t0002g0141 | 2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.577-1759T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77379149 | ||||||
| chr7:77379231
|
T | C | 1 | a0002c0003t0001g0287 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.577-1841A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77379231 | ||||||
| chr7:77379461
|
G | A | 2 | a0007c0011t0002g0209a0007c0011t0002g0311 | 2 | HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.576+1844C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77379461 | ||||||
| chr7:77379916
|
A | T | 1 | a0001c0001t0001g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.576+1389T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77379916 | ||||||
| chr7:77379943
|
C | T | 316 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(313): Show | 320 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.576+1362G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77379943 | ||||||
| chr7:77380002
|
T | C | 6 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.576+1303A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380002 | ||||||
| chr7:77380188
|
G | C | 26 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(23): Show | 27 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.576+1117C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380188 | ||||||
| chr7:77380231
|
A | G | 98 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(95): Show | 99 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.576+1074T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380231 | ||||||
| chr7:77380259
|
G | A | 4 | a0001c0001t0001g0236a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | NA18971.hp1 NA18978.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+1046C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380259 | ||||||
| chr7:77380353
|
T | C | 1 | a0001c0002t0001g0270 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.576+952A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380353 | ||||||
| chr7:77380366
|
A | C | 1 | a0001c0002t0001g0270 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.576+939T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380366 | ||||||
| chr7:77380382
|
G | A | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.576+923C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380382 | ||||||
| chr7:77380724
|
T | C | 1 | a0007c0011t0002g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.576+581A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380724 | ||||||
| chr7:77380813
|
G | T | 98 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.576+492C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380813 | ||||||
| chr7:77380832
|
C | T | 1 | a0001c0001t0001g0306 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.576+473G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380832 | ||||||
| chr7:77380893
|
C | T | 15 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0020others(12): Show | 16 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.576+412G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380893 | ||||||
| chr7:77380903
|
T | C | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.576+402A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380903 | ||||||
| chr7:77381263
|
G | GA | 81 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0001g0296others(78): Show | 82 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.576+41dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77381263 | ||||||
| chr7:77381365
|
AAAAC | A | 78 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(75): Show | 79 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.527-15_527-12delGT others(2): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77381365 | ||||||
| chr7:77381369
|
C | G | 1 | a0001c0021t0001g0250 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.527-15G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77381369 | ||||||
| chr7:77381392
|
A | T | 21 | a0003c0004t0001g0191a0003c0004t0002g0032a0003c0004t0002g0114others(18): Show | 21 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.527-38T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77381392 | ||||||
| chr7:77381607
|
T | C | 3 | a0001c0002t0001g0235a0001c0002t0001g0281a0001c0002t0001g0283 | 3 | NA19005.hp2 NA19011.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.527-253A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77381607 | ||||||
| chr7:77381749
|
T | C | 7 | a0001c0002t0001g0268a0001c0002t0001g0272a0001c0002t0001g0273others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.527-395A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77381749 | ||||||
| chr7:77381819
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.527-465A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77381819 | ||||||
| chr7:77381991
|
T | C | 1 | a0001c0010t0001g0151 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.526+583A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77381991 | ||||||
| chr7:77382011
|
G | A | 1 | a0001c0002t0001g0117 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.526+563C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77382011 | ||||||
| chr7:77382120
|
T | C | 10 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(7): Show | 10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.526+454A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77382120 | ||||||
| chr7:77382183
|
A | G | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.526+391T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77382183 | ||||||
| chr7:77382334
|
T | A | 1 | a0002c0018t0001g0100 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.526+240A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77382334 | ||||||
| chr7:77382410
|
A | G | 7 | a0001c0001t0001g0002a0001c0001t0001g0210a0001c0001t0001g0251others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+164T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77382410 | ||||||
| chr7:77382500
|
T | G | 11 | a0001c0028t0002g0143a0002c0027t0001g0215a0006c0008t0001g0016others(8): Show | 11 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.526+74A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77382500 | ||||||
| chr7:77382725
|
C | T | 60 | a0001c0001t0001g0002a0001c0001t0001g0210a0001c0001t0001g0251others(57): Show | 62 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.457-82G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77382725 | ||||||
| chr7:77382726
|
T | C | 7 | a0001c0001t0001g0044a0001c0001t0001g0077a0001c0001t0001g0193others(4): Show | 7 | HG00544.hp1 NA18983.hp1 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.457-83A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77382726 | ||||||
| chr7:77382950
|
C | G | 1 | a0005c0006t0001g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.457-307G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77382950 | ||||||
| chr7:77383036
|
G | A | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.457-393C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383036 | ||||||
| chr7:77383098
|
G | T | 1 | a0001c0002t0001g0298 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.457-455C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383098 | ||||||
| chr7:77383185
|
T | C | 74 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(71): Show | 75 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.457-542A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383185 | ||||||
| chr7:77383318
|
T | TCA | 10 | a0001c0001t0001g0259a0001c0002t0001g0158a0001c0002t0001g0194others(7): Show | 10 | HG00558.hp1 HG01261.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.457-677_457-676dup others(2): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383318 | ||||||
| chr7:77383318
|
TCA | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(151): Show | 155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.457-677_457-676del others(2): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383318 | ||||||
| chr7:77383318
|
TCACA | T | 23 | a0001c0002t0002g0008a0001c0002t0002g0010a0001c0002t0002g0013others(20): Show | 23 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.457-679_457-676del others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383318 | ||||||
| chr7:77383520
|
T | A | 81 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(78): Show | 82 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.457-877A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383520 | ||||||
| chr7:77383648
|
A | G | 83 | a0001c0001t0001g0007a0001c0001t0001g0296a0001c0001t0001g0297others(80): Show | 84 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.457-1005T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383648 | ||||||
| chr7:77383714
|
C | A | 1 | a0001c0001t0001g0198 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.457-1071G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383714 | ||||||
| chr7:77383728
|
C | T | 74 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(71): Show | 75 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.457-1085G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383728 | ||||||
| chr7:77383854
|
G | C | 2 | a0001c0002t0002g0136a0001c0002t0002g0141 | 2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.457-1211C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383854 | ||||||
| chr7:77383860
|
T | A | 1 | a0001c0002t0001g0194 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.457-1217A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383860 | ||||||
| chr7:77383930
|
A | C | 1 | a0001c0002t0001g0282 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.457-1287T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383930 | ||||||
| chr7:77384000
|
T | C | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.457-1357A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77384000 | ||||||
| chr7:77384075
|
A | G | 16 | a0001c0028t0002g0143a0002c0027t0001g0215a0003c0004t0002g0032others(13): Show | 16 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.457-1432T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77384075 | ||||||
| chr7:77384275
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.457-1632T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77384275 | ||||||
| chr7:77384277
|
G | A | 16 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0020others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.457-1634C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77384277 | ||||||
| chr7:77384406
|
G | T | 5 | a0002c0003t0002g0054a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.457-1763C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77384406 | ||||||
| chr7:77384578
|
G | A | 1 | a0004c0005t0003g0161 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.457-1935C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77384578 | ||||||
| chr7:77384660
|
G | A | 10 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(7): Show | 10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.457-2017C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77384660 | ||||||
| chr7:77384868
|
G | A | 1 | a0006c0008t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.457-2225C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77384868 | ||||||
| chr7:77384947
|
T | G | 5 | a0001c0001t0001g0043a0001c0001t0001g0071a0001c0001t0001g0073others(2): Show | 5 | HG00735.hp1 HG00738.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.457-2304A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77384947 | ||||||
| chr7:77385034
|
C | CT | 15 | a0001c0001t0001g0258a0001c0002t0002g0008a0001c0002t0002g0009others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.456+2325dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385034 | ||||||
| chr7:77385090
|
A | G | 10 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(7): Show | 10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.456+2270T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385090 | ||||||
| chr7:77385113
|
A | C | 26 | a0001c0001t0001g0043a0001c0001t0001g0071a0001c0001t0001g0073others(23): Show | 26 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.456+2247T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385113 | ||||||
| chr7:77385158
|
C | T | 1 | a0001c0002t0001g0303 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.456+2202G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385158 | ||||||
| chr7:77385190
|
C | T | 1 | a0002c0003t0001g0122 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.456+2170G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385190 | ||||||
| chr7:77385220
|
G | T | 1 | a0001c0001t0001g0115 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.456+2140C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385220 | ||||||
| chr7:77385432
|
T | C | 1 | a0001c0002t0001g0119 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.456+1928A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385432 | ||||||
| chr7:77385830
|
A | G | 1 | a0001c0002t0001g0266 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.456+1530T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385830 | ||||||
| chr7:77385974
|
A | G | 3 | a0001c0002t0002g0120a0001c0002t0002g0183a0001c0002t0004g0033 | 3 | HG01243.hp1 HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.456+1386T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385974 | ||||||
| chr7:77385979
|
A | C | 1 | a0001c0002t0001g0242 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.456+1381T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385979 | ||||||
| chr7:77385990
|
T | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0206 | 3 | HG01257.hp1 HG01258.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.456+1370A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385990 | ||||||
| chr7:77386059
|
G | GA | 133 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0071others(130): Show | 136 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.456+1300dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386059 | ||||||
| chr7:77386094
|
C | T | 12 | a0002c0003t0001g0057a0002c0003t0001g0248a0002c0003t0001g0288others(9): Show | 13 | NA18946.hp2 NA18949.hp1 NA18966.hp1 others(10): Show |
intron_variant | MODIFIER | c.456+1266G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386094 | ||||||
| chr7:77386381
|
T | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0071others(162): Show | 168 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.456+979A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386381 | ||||||
| chr7:77386412
|
G | A | 1 | a0001c0002t0002g0141 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.456+948C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386412 | ||||||
| chr7:77386547
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.456+813G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386547 | ||||||
| chr7:77386558
|
G | A | 15 | a0004c0005t0001g0172a0004c0005t0003g0116a0004c0005t0003g0160others(12): Show | 15 | HG00558.hp2 HG00621.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.456+802C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386558 | ||||||
| chr7:77386617
|
C | T | 4 | a0001c0010t0001g0146a0001c0010t0001g0150a0001c0010t0001g0151others(1): Show | 4 | HG03139.hp2 HG03516.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.456+743G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386617 | ||||||
| chr7:77386716
|
G | A | 14 | a0001c0028t0002g0143a0002c0003t0002g0054a0002c0027t0001g0215others(11): Show | 14 | HG00639.hp1 HG01109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.456+644C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386716 | ||||||
| chr7:77386746
|
T | C | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.456+614A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386746 | ||||||
| chr7:77386805
|
G | A | 4 | a0002c0003t0001g0020a0002c0003t0001g0246a0002c0003t0001g0247others(1): Show | 4 | NA18963.hp1 NA19003.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.456+555C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386805 | ||||||
| chr7:77386865
|
C | T | 11 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(8): Show | 11 | HG01433.hp2 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.456+495G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386865 | ||||||
| chr7:77386960
|
G | T | 2 | a0001c0002t0001g0265a0001c0002t0001g0275 | 2 | HG00673.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.456+400C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386960 | ||||||
| chr7:77386991
|
T | C | 4 | a0001c0002t0002g0001a0001c0002t0002g0208a0001c0002t0002g0220others(1): Show | 5 | HG01884.hp1 HG02109.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.456+369A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386991 | ||||||
| chr7:77387033
|
C | T | 2 | a0001c0002t0002g0136a0001c0002t0002g0141 | 2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.456+327G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77387033 | ||||||
| chr7:77387043
|
T | C | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.456+317A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77387043 | ||||||
| chr7:77387143
|
T | C | 10 | a0001c0028t0002g0143a0002c0027t0001g0215a0006c0008t0001g0016others(7): Show | 10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.456+217A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77387143 | ||||||
| chr7:77387169
|
T | C | 1 | a0002c0003t0001g0320 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.456+191A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77387169 | ||||||
| chr7:77387230
|
G | A | 1 | a0005c0006t0001g0123 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.456+130C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77387230 | ||||||
| chr7:77387242
|
T | A | 2 | a0001c0002t0002g0136a0001c0002t0002g0141 | 2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.456+118A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77387242 | ||||||
| chr7:77387332
|
A | G | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.456+28T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77387332 | ||||||
| chr7:77387510
|
A | C | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.368-62T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77387510 | ||||||
| chr7:77387563
|
A | T | 1 | a0001c0002t0001g0277 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.368-115T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77387563 | ||||||
| chr7:77387650
|
C | T | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.368-202G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77387650 | ||||||
| chr7:77387651
|
G | A | 2 | a0002c0003t0001g0068a0002c0003t0003g0067 | 2 | HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.368-203C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77387651 | ||||||
| chr7:77387747
|
C | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0077a0001c0001t0001g0193others(4): Show | 7 | HG00544.hp1 NA18983.hp1 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.368-299G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77387747 | ||||||
| chr7:77387787
|
T | C | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.368-339A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77387787 | ||||||
| chr7:77387953
|
G | A | 1 | a0001c0002t0001g0278 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.368-505C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77387953 | ||||||
| chr7:77388026
|
T | C | 10 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(7): Show | 10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.368-578A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77388026 | ||||||
| chr7:77388081
|
A | G | 1 | a0001c0023t0001g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.368-633T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77388081 | ||||||
| chr7:77388125
|
T | C | 198 | a0001c0001t0001g0205a0001c0001t0001g0296a0001c0001t0001g0297others(195): Show | 201 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.368-677A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77388125 | ||||||
| chr7:77388269
|
G | A | 1 | a0006c0008t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.368-821C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77388269 | ||||||
| chr7:77388345
|
T | C | 10 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(7): Show | 10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.368-897A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77388345 | ||||||
| chr7:77388577
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0040others(2): Show | 5 | HG00408.hp2 HG00423.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.368-1129G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77388577 | ||||||
| chr7:77388578
|
G | A | 4 | a0003c0004t0002g0124a0003c0004t0002g0125a0003c0004t0002g0134others(1): Show | 4 | HG00140.hp1 HG01993.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.368-1130C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77388578 | ||||||
| chr7:77388779
|
C | T | 1 | a0001c0002t0002g0141 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.368-1331G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77388779 | ||||||
| chr7:77388866
|
CAGTA | C | 6 | a0001c0001t0001g0327a0001c0001t0001g0329a0001c0001t0001g0330others(3): Show | 6 | HG00597.hp2 HG02015.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.368-1422_368-1419d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77388866 | ||||||
| chr7:77388996
|
A | G | 1 | a0012c0022t0001g0130 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.368-1548T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77388996 | ||||||
| chr7:77389108
|
T | C | 6 | a0001c0028t0002g0143a0006c0008t0001g0051a0006c0008t0001g0135others(3): Show | 6 | HG00639.hp1 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.368-1660A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389108 | ||||||
| chr7:77389132
|
A | G | 2 | a0001c0002t0001g0194a0001c0002t0001g0274 | 2 | HG02071.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.368-1684T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389132 | ||||||
| chr7:77389195
|
G | A | 2 | a0001c0002t0001g0244a0001c0002t0001g0263 | 2 | HG03831.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.368-1747C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389195 | ||||||
| chr7:77389225
|
C | T | 316 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(313): Show | 320 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.368-1777G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389225 | ||||||
| chr7:77389232
|
G | A | 1 | a0001c0002t0001g0144 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.368-1784C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389232 | ||||||
| chr7:77389260
|
A | T | 16 | a0001c0001t0001g0259a0003c0004t0001g0191a0003c0004t0002g0114others(13): Show | 16 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.368-1812T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389260 | ||||||
| chr7:77389262
|
T | A | 1 | a0001c0002t0002g0129 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.368-1814A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389262 | ||||||
| chr7:77389289
|
G | GTA | 3 | a0001c0002t0002g0136a0001c0002t0002g0141a0002c0027t0001g0215 | 3 | HG01109.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.368-1843_368-1842d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389289 | ||||||
| chr7:77389291
|
A | G | 5 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.368-1843T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389291 | ||||||
| chr7:77389303
|
A | T | 14 | a0001c0001t0001g0205a0001c0002t0001g0277a0001c0002t0001g0303others(11): Show | 14 | HG00642.hp2 HG02523.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.368-1855T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389303 | ||||||
| chr7:77389323
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.368-1875C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389323 | ||||||
| chr7:77389325
|
TTTG | T | 15 | a0001c0028t0002g0143a0002c0003t0002g0054a0002c0027t0001g0215others(12): Show | 15 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.368-1880_368-1878d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389325 | ||||||
| chr7:77389379
|
T | TA | 8 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0043others(5): Show | 8 | HG00735.hp1 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.368-1932dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389379 | ||||||
| chr7:77389409
|
G | T | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.368-1961C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389409 | ||||||
| chr7:77389431
|
T | TC | 13 | a0001c0001t0001g0085a0001c0001t0001g0292a0001c0001t0001g0330others(10): Show | 13 | HG00597.hp1 HG01993.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.368-1984dupG | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389431 | ||||||
| chr7:77389437
|
C | T | 2 | a0006c0008t0001g0016a0006c0008t0001g0137 | 2 | HG01074.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.368-1989G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389437 | ||||||
| chr7:77389438
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.368-1990G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389438 | ||||||
| chr7:77389457
|
C | T | 1 | a0003c0004t0002g0124 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.368-2009G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389457 | ||||||
| chr7:77389528
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.368-2080C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389528 | ||||||
| chr7:77389530
|
G | A | 59 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(56): Show | 60 | HG00738.hp1 HG01257.hp2 HG01433.hp2 others(57): Show |
intron_variant | MODIFIER | c.368-2082C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389530 | ||||||
| chr7:77389668
|
T | G | 1 | a0002c0003t0001g0286 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.368-2220A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389668 | ||||||
| chr7:77389844
|
T | C | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.368-2396A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389844 | ||||||
| chr7:77389912
|
T | C | 10 | a0001c0028t0002g0143a0002c0027t0001g0215a0006c0008t0001g0016others(7): Show | 10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.368-2464A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389912 | ||||||
| chr7:77389917
|
C | T | 10 | a0001c0028t0002g0143a0002c0027t0001g0215a0006c0008t0001g0016others(7): Show | 10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.368-2469G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389917 | ||||||
| chr7:77389992
|
A | G | 2 | a0001c0001t0001g0050a0001c0002t0002g0141 | 2 | HG02074.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.368-2544T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389992 | ||||||
| chr7:77390007
|
T | A | 1 | a0001c0001t0001g0226 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.368-2559A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390007 | ||||||
| chr7:77390020
|
G | T | 4 | a0001c0001t0001g0050a0002c0003t0001g0216a0002c0003t0001g0217others(1): Show | 4 | HG02074.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.368-2572C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390020 | ||||||
| chr7:77390039
|
C | G | 1 | a0001c0001t0001g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.368-2591G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390039 | ||||||
| chr7:77390141
|
C | T | 95 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(92): Show | 97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.368-2693G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390141 | ||||||
| chr7:77390170
|
G | C | 1 | a0002c0003t0001g0004 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.368-2722C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390170 | ||||||
| chr7:77390295
|
C | T | 2 | a0001c0010t0001g0015a0014c0017t0001g0348 | 2 | HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.368-2847G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390295 | ||||||
| chr7:77390425
|
A | G | 1 | a0001c0002t0001g0019 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.368-2977T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390425 | ||||||
| chr7:77390452
|
A | G | 73 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(70): Show | 74 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.368-3004T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390452 | ||||||
| chr7:77390549
|
A | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(119): Show | 123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.368-3101T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390549 | ||||||
| chr7:77390656
|
T | C | 117 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(114): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.368-3208A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390656 | ||||||
| chr7:77390821
|
C | T | 49 | a0002c0003t0001g0037a0002c0003t0001g0047a0002c0003t0001g0057others(46): Show | 50 | HG00738.hp1 HG01257.hp2 HG01884.hp2 others(47): Show |
intron_variant | MODIFIER | c.368-3373G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390821 | ||||||
| chr7:77390939
|
C | T | 2 | a0003c0004t0002g0153a0003c0004t0002g0154 | 2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.368-3491G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390939 | ||||||
| chr7:77390946
|
T | TA | 49 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0045others(46): Show | 49 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.368-3499dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
T | TAA | 48 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0022others(45): Show | 48 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.368-3500_368-3499d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
T | TAAA | 29 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0042others(26): Show | 29 | HG00099.hp2 HG00597.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.368-3501_368-3499d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
T | TAAAA | 6 | a0001c0001t0001g0041a0001c0001t0001g0048a0001c0001t0001g0071others(3): Show | 6 | HG01070.hp2 HG01517.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.368-3502_368-3499d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
T | TAAAAA | 7 | a0001c0001t0001g0043a0001c0001t0001g0073a0001c0001t0001g0080others(4): Show | 7 | HG00735.hp1 HG00738.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.368-3503_368-3499d others(7): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
T | TAAAAAAA others(4): Show |
1 | a0003c0004t0002g0188 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.368-3509_368-3499d others(13): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
T | TAAAAAAA others(5): Show |
3 | a0003c0004t0002g0184a0003c0004t0002g0185a0003c0004t0005g0186 | 3 | HG03098.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.368-3510_368-3499d others(14): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
T | TAAAAAAA others(6): Show |
1 | a0003c0004t0002g0133 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.368-3511_368-3499d others(15): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
T | TAAAAAAA others(8): Show |
1 | a0003c0004t0002g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.368-3513_368-3499d others(17): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
T | TTAAAAAA others(4): Show |
1 | a0003c0004t0002g0147 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.368-3499_368-3498i others(13): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
TA | T | 23 | a0001c0002t0001g0118a0001c0002t0001g0231a0001c0002t0001g0234others(20): Show | 23 | HG00597.hp1 HG00639.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.368-3499delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
TAA | T | 11 | a0001c0002t0001g0119a0001c0002t0001g0240a0001c0002t0001g0266others(8): Show | 12 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(9): Show |
intron_variant | MODIFIER | c.368-3500_368-3499d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
TAAA | T | 25 | a0001c0002t0001g0019a0001c0002t0001g0024a0001c0002t0001g0111others(22): Show | 26 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.368-3501_368-3499d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
TAAAA | T | 31 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(28): Show | 31 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.368-3502_368-3499d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
TAAAAAAA others(1): Show |
T | 7 | a0003c0004t0002g0114a0003c0004t0002g0124a0003c0004t0002g0125others(4): Show | 7 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.368-3506_368-3499d others(10): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
TAAAAAAA others(3): Show |
T | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.368-3508_368-3499d others(12): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
TAAAAAAA others(6): Show |
T | 1 | a0003c0009t0001g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.368-3511_368-3499d others(15): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
TAAAAAAA others(7): Show |
T | 1 | a0012c0022t0001g0130 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.368-3512_368-3499d others(16): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
TAAAAAAA others(8): Show |
T | 1 | a0001c0002t0001g0269 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.368-3513_368-3499d others(17): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
TAAAAAAA others(12): Show |
T | 1 | a0003c0004t0001g0191 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.368-3517_368-3499d others(21): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
TAAAAAAA others(16): Show |
T | 2 | a0002c0003t0001g0248a0002c0007t0001g0326 | 2 | NA18949.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.368-3521_368-3499d others(25): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
TAAAAAAA others(17): Show |
T | 50 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0097others(47): Show | 51 | HG00738.hp1 HG01099.hp1 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.368-3522_368-3499d others(26): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390946
|
TAAAAAAA others(18): Show |
T | 2 | a0003c0004t0002g0153a0003c0004t0002g0154 | 2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.368-3523_368-3499d others(27): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | ||||||
| chr7:77390954
|
A | T | 1 | a0003c0004t0002g0157 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.368-3506T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390954 | ||||||
| chr7:77390955
|
A | T | 7 | a0003c0004t0002g0114a0003c0004t0002g0124a0003c0004t0002g0125others(4): Show | 7 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.368-3507T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390955 | ||||||
| chr7:77390956
|
A | T | 1 | a0003c0004t0002g0204 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.368-3508T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390956 | ||||||
| chr7:77390960
|
A | T | 1 | a0003c0009t0001g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.368-3512T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390960 | ||||||
| chr7:77390966
|
A | T | 1 | a0003c0004t0001g0191 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.368-3518T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390966 | ||||||
| chr7:77390972
|
A | T | 2 | a0003c0004t0002g0153a0003c0004t0002g0154 | 2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.368-3524T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390972 | ||||||
| chr7:77391020
|
G | A | 9 | a0001c0002t0002g0001a0001c0002t0002g0126a0001c0002t0002g0131others(6): Show | 10 | HG01192.hp2 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.368-3572C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391020 | ||||||
| chr7:77391120
|
C | T | 1 | a0003c0009t0001g0192 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.368-3672G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391120 | ||||||
| chr7:77391125
|
C | CA | 46 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0041others(43): Show | 46 | HG00140.hp2 HG00408.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.368-3678dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391125 | ||||||
| chr7:77391125
|
C | CAA | 19 | a0001c0001t0001g0002a0001c0001t0001g0251a0001c0001t0001g0253others(16): Show | 21 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.368-3679_368-3678d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391125 | ||||||
| chr7:77391125
|
C | CAAA | 61 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(58): Show | 61 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.368-3680_368-3678d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391125 | ||||||
| chr7:77391125
|
CA | C | 26 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0002t0001g0344others(23): Show | 26 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.368-3678delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391125 | ||||||
| chr7:77391125
|
CAA | C | 20 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0029others(17): Show | 21 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.368-3679_368-3678d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391125 | ||||||
| chr7:77391125
|
CAAA | C | 66 | a0002c0003t0001g0020a0002c0003t0001g0037a0002c0003t0001g0047others(63): Show | 67 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.368-3680_368-3678d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391125 | ||||||
| chr7:77391136
|
A | G | 1 | a0002c0003t0001g0148 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.368-3688T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391136 | ||||||
| chr7:77391142
|
A | G | 40 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0321others(37): Show | 41 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.368-3694T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391142 | ||||||
| chr7:77391150
|
A | G | 1 | a0001c0001t0001g0306 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.368-3702T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391150 | ||||||
| chr7:77391164
|
A | C | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.368-3716T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391164 | ||||||
| chr7:77391178
|
C | CT | 23 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0218others(20): Show | 23 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.368-3731dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391178 | ||||||
| chr7:77391179
|
T | A | 1 | a0002c0003t0001g0029 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.368-3731A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391179 | ||||||
| chr7:77391188
|
T | A | 1 | a0001c0002t0001g0144 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.368-3740A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391188 | ||||||
| chr7:77391195
|
G | C | 12 | a0001c0002t0001g0118a0001c0002t0001g0194a0001c0002t0001g0231others(9): Show | 12 | HG00597.hp1 HG00673.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.368-3747C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391195 | ||||||
| chr7:77391305
|
A | G | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.368-3857T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391305 | ||||||
| chr7:77391364
|
T | C | 6 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.368-3916A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391364 | ||||||
| chr7:77391416
|
A | G | 1 | a0001c0002t0001g0238 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.368-3968T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391416 | ||||||
| chr7:77391419
|
G | A | 1 | a0001c0002t0006g0006 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.368-3971C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391419 | ||||||
| chr7:77391546
|
A | T | 64 | a0002c0003t0001g0037a0002c0003t0001g0047a0002c0003t0001g0057others(61): Show | 65 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.368-4098T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391546 | ||||||
| chr7:77391561
|
C | T | 5 | a0002c0003t0001g0037a0002c0003t0001g0061a0002c0003t0001g0062others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.368-4113G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391561 | ||||||
| chr7:77391627
|
C | T | 78 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(75): Show | 79 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.368-4179G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391627 | ||||||
| chr7:77391690
|
C | CTGGACAT others(7): Show |
1 | a0001c0002t0001g0283 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.368-4256_368-4243d others(16): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391690 | ||||||
| chr7:77391906
|
C | T | 4 | a0004c0005t0001g0172a0004c0005t0003g0160a0004c0005t0003g0165others(1): Show | 4 | HG00558.hp2 HG02027.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.368-4458G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391906 | ||||||
| chr7:77391998
|
G | A | 1 | a0006c0008t0001g0135 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.368-4550C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391998 | ||||||
| chr7:77392053
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.368-4605G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392053 | ||||||
| chr7:77392063
|
A | G | 4 | a0002c0003t0001g0020a0002c0003t0001g0246a0002c0003t0001g0247others(1): Show | 4 | NA18963.hp1 NA19003.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.368-4615T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392063 | ||||||
| chr7:77392087
|
T | C | 10 | a0001c0028t0002g0143a0002c0027t0001g0215a0006c0008t0001g0016others(7): Show | 10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.368-4639A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392087 | ||||||
| chr7:77392170
|
C | T | 1 | a0002c0003t0001g0065 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.368-4722G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392170 | ||||||
| chr7:77392180
|
C | G | 2 | a0001c0002t0002g0108a0001c0002t0002g0109 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.368-4732G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392180 | ||||||
| chr7:77392224
|
G | GAA | 80 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(77): Show | 81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.367+4756_367+4757d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392224 | ||||||
| chr7:77392266
|
G | A | 79 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(76): Show | 80 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.367+4716C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392266 | ||||||
| chr7:77392458
|
G | A | 16 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0020others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.367+4524C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392458 | ||||||
| chr7:77392463
|
G | A | 14 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0040others(11): Show | 14 | HG00408.hp2 HG00423.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.367+4519C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392463 | ||||||
| chr7:77392543
|
G | A | 1 | a0001c0002t0002g0126 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.367+4439C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392543 | ||||||
| chr7:77392644
|
A | G | 1 | a0001c0002t0001g0242 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.367+4338T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392644 | ||||||
| chr7:77392697
|
A | G | 80 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(77): Show | 81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.367+4285T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392697 | ||||||
| chr7:77392758
|
T | A | 21 | a0002c0018t0001g0100a0003c0004t0001g0191a0003c0004t0002g0032others(18): Show | 21 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.367+4224A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392758 | ||||||
| chr7:77393159
|
A | C | 81 | a0001c0001t0001g0214a0001c0001t0001g0296a0001c0001t0001g0297others(78): Show | 82 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.367+3823T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77393159 | ||||||
| chr7:77393262
|
C | A | 15 | a0001c0028t0002g0143a0002c0003t0002g0054a0002c0027t0001g0215others(12): Show | 15 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.367+3720G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77393262 | ||||||
| chr7:77393559
|
C | T | 80 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(77): Show | 81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.367+3423G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77393559 | ||||||
| chr7:77393674
|
C | CT | 26 | a0001c0001t0001g0022a0001c0002t0001g0276a0001c0002t0001g0277others(23): Show | 26 | HG01167.hp2 HG01433.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.367+3307dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77393674 | ||||||
| chr7:77393674
|
C | CTT | 70 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0306others(67): Show | 71 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.367+3306_367+3307d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77393674 | ||||||
| chr7:77393674
|
C | CTTT | 6 | a0001c0001t0001g0305a0001c0002t0001g0110a0001c0002t0001g0233others(3): Show | 6 | HG02132.hp1 NA18948.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.367+3305_367+3307d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77393674 | ||||||
| chr7:77393818
|
C | T | 1 | a0006c0008t0001g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.367+3164G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77393818 | ||||||
| chr7:77393834
|
C | T | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.367+3148G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77393834 | ||||||
| chr7:77393865
|
G | C | 80 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(77): Show | 81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.367+3117C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77393865 | ||||||
| chr7:77393866
|
G | C | 1 | a0001c0002t0001g0052 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.367+3116C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77393866 | ||||||
| chr7:77394038
|
T | C | 80 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(77): Show | 81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.367+2944A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394038 | ||||||
| chr7:77394090
|
C | T | 67 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(64): Show | 67 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.367+2892G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394090 | ||||||
| chr7:77394098
|
A | G | 1 | a0002c0003t0001g0347 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.367+2884T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394098 | ||||||
| chr7:77394185
|
T | C | 20 | a0001c0028t0002g0143a0002c0003t0002g0054a0002c0027t0001g0215others(17): Show | 20 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.367+2797A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394185 | ||||||
| chr7:77394646
|
G | A | 1 | a0001c0002t0001g0283 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.367+2336C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394646 | ||||||
| chr7:77394715
|
T | C | 2 | a0001c0002t0002g0108a0001c0002t0002g0109 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.367+2267A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394715 | ||||||
| chr7:77394740
|
T | A | 1 | a0001c0002t0001g0254 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.367+2242A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394740 | ||||||
| chr7:77394745
|
C | T | 1 | a0006c0008t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.367+2237G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394745 | ||||||
| chr7:77394813
|
T | C | 1 | a0002c0003t0002g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.367+2169A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394813 | ||||||
| chr7:77394814
|
A | G | 5 | a0002c0003t0002g0054a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.367+2168T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394814 | ||||||
| chr7:77394960
|
C | T | 174 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(171): Show | 176 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(173): Show |
intron_variant | MODIFIER | c.367+2022G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394960 | ||||||
| chr7:77394983
|
C | T | 191 | a0001c0001t0001g0205a0001c0001t0001g0296a0001c0001t0001g0297others(188): Show | 194 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.367+1999G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394983 | ||||||
| chr7:77395162
|
G | C | 17 | a0001c0001t0001g0205a0002c0003t0001g0004a0002c0003t0001g0018others(14): Show | 18 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.367+1820C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77395162 | ||||||
| chr7:77395170
|
TAGAC | T | 77 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(74): Show | 78 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.367+1808_367+1811d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77395170 | ||||||
| chr7:77395292
|
A | C | 1 | a0001c0010t0001g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.367+1690T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77395292 | ||||||
| chr7:77395370
|
A | G | 1 | a0002c0003t0001g0286 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.367+1612T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77395370 | ||||||
| chr7:77395442
|
G | A | 3 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0028t0002g0143 | 3 | HG02109.hp1 HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.367+1540C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77395442 | ||||||
| chr7:77395497
|
A | G | 1 | a0006c0008t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.367+1485T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77395497 | ||||||
| chr7:77395813
|
G | A | 1 | a0004c0005t0001g0106 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.367+1169C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77395813 | ||||||
| chr7:77395845
|
A | T | 314 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(311): Show | 318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.367+1137T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77395845 | ||||||
| chr7:77396190
|
T | G | 2 | a0001c0002t0002g0108a0001c0002t0002g0109 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.367+792A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77396190 | ||||||
| chr7:77396240
|
C | A | 47 | a0002c0003t0001g0037a0002c0003t0001g0047a0002c0003t0001g0057others(44): Show | 48 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(45): Show |
intron_variant | MODIFIER | c.367+742G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77396240 | ||||||
| chr7:77396343
|
T | C | 1 | a0006c0008t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.367+639A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77396343 | ||||||
| chr7:77396449
|
G | T | 9 | a0003c0004t0002g0114a0003c0004t0002g0124a0003c0004t0002g0125others(6): Show | 9 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+533C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77396449 | ||||||
| chr7:77396723
|
T | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(119): Show | 123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.367+259A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77396723 | ||||||
| chr7:77396818
|
AT | A | 12 | a0001c0002t0002g0001a0001c0002t0002g0120a0001c0002t0002g0126others(9): Show | 13 | HG01192.hp2 HG01243.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.367+163delA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77396818 | ||||||
| chr7:77396819
|
T | A | 48 | a0001c0001t0001g0193a0001c0001t0001g0293a0002c0003t0001g0037others(45): Show | 49 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(46): Show |
intron_variant | MODIFIER | c.367+163A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77396819 | ||||||
| chr7:77397047
|
A | G | 2 | a0001c0002t0002g0108a0001c0002t0002g0109 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.314-12T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 4/30 | chr7 | 77397047 | ||||||
| chr7:77397133
|
A | G | 2 | a0003c0004t0002g0153a0003c0004t0002g0154 | 2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.314-98T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 4/30 | chr7 | 77397133 | ||||||
| chr7:77397143
|
G | A | 62 | a0002c0003t0001g0037a0002c0003t0001g0047a0002c0003t0001g0057others(59): Show | 63 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.314-108C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 4/30 | chr7 | 77397143 | ||||||
| chr7:77397759
|
A | C | 81 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(78): Show | 82 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.244-344T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77397759 | ||||||
| chr7:77397778
|
T | A | 1 | a0006c0008t0001g0140 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.244-363A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77397778 | ||||||
| chr7:77398036
|
T | G | 4 | a0007c0011t0002g0139a0007c0011t0002g0145a0007c0011t0002g0209others(1): Show | 4 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-621A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77398036 | ||||||
| chr7:77398211
|
G | T | 16 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0020others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.244-796C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77398211 | ||||||
| chr7:77398397
|
TCTAA | T | 10 | a0001c0028t0002g0143a0002c0027t0001g0215a0006c0008t0001g0016others(7): Show | 10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.244-986_244-983del others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77398397 | ||||||
| chr7:77398614
|
A | T | 6 | a0001c0002t0001g0266a0001c0002t0002g0136a0001c0002t0002g0141others(3): Show | 6 | HG02896.hp2 HG02897.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-1199T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77398614 | ||||||
| chr7:77398771
|
C | CA | 79 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(76): Show | 80 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.244-1357dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77398771 | ||||||
| chr7:77398973
|
C | T | 80 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(77): Show | 81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.244-1558G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77398973 | ||||||
| chr7:77399013
|
G | T | 1 | a0001c0002t0002g0010 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.244-1598C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399013 | ||||||
| chr7:77399137
|
T | A | 80 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(77): Show | 81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.244-1722A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399137 | ||||||
| chr7:77399182
|
T | A | 1 | a0003c0009t0001g0192 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.244-1767A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399182 | ||||||
| chr7:77399335
|
G | T | 7 | a0002c0007t0001g0228a0002c0007t0001g0229a0002c0007t0001g0230others(4): Show | 7 | NA18946.hp2 NA18978.hp2 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.244-1920C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399335 | ||||||
| chr7:77399504
|
C | A | 1 | a0001c0002t0002g0001 | 2 | HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.244-2089G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399504 | ||||||
| chr7:77399528
|
C | T | 1 | a0013c0025t0001g0307 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.244-2113G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399528 | ||||||
| chr7:77399667
|
T | C | 80 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(77): Show | 81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.244-2252A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399667 | ||||||
| chr7:77399703
|
TG | T | 58 | a0001c0001t0001g0074a0001c0001t0001g0199a0001c0001t0001g0200others(55): Show | 59 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.244-2289delC | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399703 | ||||||
| chr7:77399711
|
G | A | 2 | a0001c0002t0002g0136a0001c0002t0002g0141 | 2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.244-2296C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399711 | ||||||
| chr7:77399713
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.244-2298G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399713 | ||||||
| chr7:77399786
|
T | A | 1 | a0001c0001t0001g0030 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.244-2371A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399786 | ||||||
| chr7:77400020
|
A | G | 80 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(77): Show | 81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.244-2605T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400020 | ||||||
| chr7:77400053
|
G | C | 80 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(77): Show | 81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.244-2638C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400053 | ||||||
| chr7:77400074
|
G | T | 1 | a0004c0005t0003g0116 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.244-2659C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400074 | ||||||
| chr7:77400139
|
T | C | 15 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(12): Show | 15 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.244-2724A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400139 | ||||||
| chr7:77400149
|
T | G | 1 | a0001c0002t0001g0278 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.244-2734A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400149 | ||||||
| chr7:77400232
|
G | C | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.244-2817C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400232 | ||||||
| chr7:77400315
|
C | T | 1 | a0001c0001t0001g0096 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.244-2900G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400315 | ||||||
| chr7:77400921
|
A | T | 81 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(78): Show | 82 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.244-3506T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400921 | ||||||
| chr7:77400936
|
A | AT | 144 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(141): Show | 146 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.244-3522dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400936 | ||||||
| chr7:77400936
|
AT | A | 24 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0226others(21): Show | 24 | HG00099.hp1 HG00639.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.244-3522delA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400936 | ||||||
| chr7:77400986
|
T | G | 1 | a0001c0001t0001g0070 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.244-3571A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400986 | ||||||
| chr7:77401016
|
T | C | 9 | a0001c0002t0002g0001a0001c0002t0002g0126a0001c0002t0002g0131others(6): Show | 10 | HG01192.hp2 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.243+3543A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401016 | ||||||
| chr7:77401025
|
T | G | 2 | a0005c0006t0001g0167a0005c0006t0001g0168 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.243+3534A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401025 | ||||||
| chr7:77401057
|
A | G | 81 | a0001c0001t0001g0214a0001c0001t0001g0296a0001c0001t0001g0297others(78): Show | 82 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.243+3502T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401057 | ||||||
| chr7:77401089
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.243+3470C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401089 | ||||||
| chr7:77401225
|
G | A | 1 | a0002c0003t0001g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.243+3334C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401225 | ||||||
| chr7:77401238
|
A | G | 1 | a0002c0003t0001g0336 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.243+3321T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401238 | ||||||
| chr7:77401244
|
G | A | 5 | a0002c0003t0002g0054a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.243+3315C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401244 | ||||||
| chr7:77401323
|
A | G | 1 | a0001c0002t0002g0109 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.243+3236T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401323 | ||||||
| chr7:77401620
|
C | A | 80 | a0001c0001t0001g0214a0001c0001t0001g0296a0001c0001t0001g0297others(77): Show | 81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.243+2939G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401620 | ||||||
| chr7:77401789
|
C | T | 6 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+2770G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401789 | ||||||
| chr7:77401839
|
A | T | 9 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(6): Show | 9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.243+2720T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401839 | ||||||
| chr7:77401930
|
A | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG01168.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.243+2629T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401930 | ||||||
| chr7:77402017
|
T | C | 2 | a0002c0003t0001g0248a0002c0003t0001g0288 | 2 | NA18949.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.243+2542A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402017 | ||||||
| chr7:77402042
|
G | C | 1 | a0001c0002t0001g0242 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.243+2517C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402042 | ||||||
| chr7:77402076
|
C | G | 80 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(77): Show | 81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.243+2483G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402076 | ||||||
| chr7:77402402
|
G | GA | 11 | a0003c0004t0002g0133a0003c0004t0002g0153a0003c0004t0002g0154others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.243+2156dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402402 | ||||||
| chr7:77402402
|
GAA | G | 68 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(65): Show | 69 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.243+2155_243+2156d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402402 | ||||||
| chr7:77402404
|
A | G | 1 | a0001c0002t0001g0233 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.243+2155T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402404 | ||||||
| chr7:77402409
|
A | AT | 33 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(30): Show | 33 | HG01099.hp1 HG01168.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.243+2149_243+2150i others(3): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402409 | ||||||
| chr7:77402409
|
A | T | 9 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(6): Show | 9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.243+2150T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402409 | ||||||
| chr7:77402411
|
A | AT | 24 | a0001c0001t0001g0255a0002c0003t0001g0064a0002c0003t0001g0248others(21): Show | 25 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.243+2147_243+2148i others(3): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402411 | ||||||
| chr7:77402411
|
A | T | 181 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(178): Show | 182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.243+2148T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402411 | ||||||
| chr7:77402411
|
AAT | A | 10 | a0001c0002t0001g0194a0001c0002t0001g0235a0001c0002t0001g0243others(7): Show | 10 | HG00673.hp2 HG02071.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.243+2146_243+2147d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402411 | ||||||
| chr7:77402413
|
T | A | 4 | a0003c0004t0001g0191a0003c0009t0001g0028a0003c0009t0001g0192others(1): Show | 4 | HG01255.hp1 HG02523.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.243+2146A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402413 | ||||||
| chr7:77402425
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.243+2134G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402425 | ||||||
| chr7:77402435
|
G | A | 88 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(85): Show | 89 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.243+2124C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402435 | ||||||
| chr7:77402435
|
G | C | 21 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0020others(18): Show | 22 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.243+2124C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402435 | ||||||
| chr7:77402455
|
C | T | 22 | a0002c0018t0001g0100a0003c0004t0001g0191a0003c0004t0002g0032others(19): Show | 22 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.243+2104G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402455 | ||||||
| chr7:77402497
|
A | AG | 3 | a0005c0006t0001g0132a0005c0006t0001g0167a0005c0006t0001g0168 | 3 | HG00099.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.243+2061dupC | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402497 | ||||||
| chr7:77402593
|
C | CAAAAAA | 9 | a0002c0018t0001g0100a0003c0004t0002g0124a0003c0004t0002g0125others(6): Show | 9 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.243+1960_243+1965d others(8): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | ||||||
| chr7:77402593
|
C | CAAAAAAA | 11 | a0003c0004t0001g0191a0003c0004t0002g0032a0003c0004t0002g0114others(8): Show | 11 | HG02523.hp2 HG02717.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.243+1959_243+1965d others(9): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | ||||||
| chr7:77402593
|
C | CAAAAAAA others(6): Show |
2 | a0001c0002t0002g0108a0001c0002t0002g0109 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.243+1953_243+1965d others(15): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | ||||||
| chr7:77402593
|
C | CAAAAAAA others(13): Show |
2 | a0002c0003t0001g0004a0002c0003t0001g0029 | 3 | HG00280.hp2 HG00323.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.243+1946_243+1965d others(22): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | ||||||
| chr7:77402593
|
C | CAAAAAAA others(14): Show |
2 | a0002c0003t0001g0079a0006c0020t0003g0023 | 2 | HG02735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.243+1945_243+1965d others(23): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | ||||||
| chr7:77402593
|
C | CAAAAAAA others(15): Show |
4 | a0001c0001t0001g0205a0002c0003t0001g0018a0002c0003t0001g0156others(1): Show | 4 | HG00642.hp2 HG02015.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+1944_243+1965d others(24): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | ||||||
| chr7:77402593
|
C | CAAAAAAA others(16): Show |
1 | a0002c0003t0001g0103 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.243+1943_243+1965d others(25): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | ||||||
| chr7:77402593
|
C | CAAAAAAA others(17): Show |
3 | a0002c0003t0001g0102a0002c0003t0001g0104a0012c0022t0001g0130 | 3 | HG01123.hp2 HG01517.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.243+1965_243+1966i others(26): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | ||||||
| chr7:77402593
|
CA | C | 52 | a0001c0001t0001g0306a0001c0002t0001g0279a0001c0002t0001g0344others(49): Show | 53 | HG00423.hp1 HG01168.hp2 HG01169.hp2 others(50): Show |
intron_variant | MODIFIER | c.243+1965delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | ||||||
| chr7:77402593
|
CAA | C | 81 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(78): Show | 82 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.243+1964_243+1965d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | ||||||
| chr7:77402593
|
CAAAA | C | 14 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(11): Show | 14 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.243+1962_243+1965d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | ||||||
| chr7:77402616
|
A | AAAAAAAA others(24): Show |
1 | a0001c0001t0001g0034 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.243+1942_243+1943i others(33): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | ||||||
| chr7:77402616
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0083 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.243+1942_243+1943i others(32): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | ||||||
| chr7:77402616
|
A | AAAAAAAA others(22): Show |
1 | a0001c0001t0001g0334 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.243+1942_243+1943i others(31): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | ||||||
| chr7:77402616
|
A | AAAAAAAA others(21): Show |
2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG00597.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.243+1942_243+1943i others(30): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | ||||||
| chr7:77402616
|
A | AAAAAAAA others(20): Show |
7 | a0001c0001t0001g0044a0001c0001t0001g0077a0001c0001t0001g0080others(4): Show | 7 | HG01243.hp2 HG02280.hp2 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.243+1942_243+1943i others(29): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | ||||||
| chr7:77402616
|
A | AAAAAAAA others(19): Show |
2 | a0001c0001t0001g0014a0001c0001t0001g0076 | 2 | HG02630.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.243+1942_243+1943i others(28): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | ||||||
| chr7:77402616
|
A | AAAAAAAA others(18): Show |
4 | a0001c0001t0001g0113a0001c0001t0001g0322a0001c0001t0001g0333others(1): Show | 4 | HG02155.hp2 HG02451.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+1942_243+1943i others(27): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | ||||||
| chr7:77402616
|
A | AAAAAAAA others(17): Show |
5 | a0001c0001t0001g0046a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 5 | HG01361.hp1 HG01934.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.243+1942_243+1943i others(26): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | ||||||
| chr7:77402616
|
A | AAAAAAAA others(16): Show |
7 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0085others(4): Show | 7 | HG01070.hp1 HG01993.hp2 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.243+1942_243+1943i others(25): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | ||||||
| chr7:77402616
|
A | AAAAAAAA others(15): Show |
28 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(25): Show | 28 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(25): Show |
intron_variant | MODIFIER | c.243+1942_243+1943i others(24): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | ||||||
| chr7:77402616
|
A | AAAAAAAA others(14): Show |
20 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0071others(17): Show | 20 | HG00733.hp1 HG00738.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.243+1942_243+1943i others(23): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | ||||||
| chr7:77402616
|
A | AAAAAAAA others(13): Show |
8 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0021others(5): Show | 9 | HG01070.hp2 HG01071.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.243+1942_243+1943i others(22): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | ||||||
| chr7:77402616
|
A | AAAAAAAA others(11): Show |
2 | a0001c0001t0001g0082a0001c0001t0001g0329 | 2 | HG02015.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.243+1942_243+1943i others(20): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | ||||||
| chr7:77402616
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0001g0041 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.243+1942_243+1943i others(19): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | ||||||
| chr7:77402616
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.243+1942_243+1943i others(18): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | ||||||
| chr7:77402616
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0236 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.243+1942_243+1943i others(17): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | ||||||
| chr7:77402616
|
A | AAAAAAAA others(5): Show |
2 | a0001c0001t0001g0069a0001c0001t0001g0201 | 2 | HG00140.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.243+1942_243+1943i others(14): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | ||||||
| chr7:77402616
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0001g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.243+1942_243+1943i others(13): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | ||||||
| chr7:77402616
|
A | AAAAAAAA others(3): Show |
3 | a0001c0001t0001g0048a0001c0001t0001g0081a0001c0001t0001g0335 | 3 | HG00544.hp1 NA18967.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.243+1942_243+1943i others(12): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | ||||||
| chr7:77402616
|
A | AAT | 6 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG00423.hp2 HG02129.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+1942_243+1943i others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | ||||||
| chr7:77402684
|
T | TA | 14 | a0001c0001t0001g0084a0001c0001t0001g0255a0001c0002t0002g0008others(11): Show | 14 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.243+1874dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402684 | ||||||
| chr7:77402684
|
T | TAA | 76 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(73): Show | 77 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.243+1873_243+1874d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402684 | ||||||
| chr7:77402737
|
G | C | 1 | a0002c0003t0001g0102 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.243+1822C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402737 | ||||||
| chr7:77402746
|
A | G | 1 | a0002c0003t0001g0148 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.243+1813T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402746 | ||||||
| chr7:77402764
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.243+1795G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402764 | ||||||
| chr7:77402955
|
A | G | 5 | a0002c0003t0002g0054a0007c0011t0002g0139a0007c0011t0002g0145others(2): Show | 5 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.243+1604T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402955 | ||||||
| chr7:77403000
|
G | C | 2 | a0004c0005t0003g0159a0004c0005t0003g0162 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.243+1559C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403000 | ||||||
| chr7:77403057
|
G | T | 14 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(11): Show | 14 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.243+1502C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403057 | ||||||
| chr7:77403181
|
C | T | 69 | a0002c0003t0001g0037a0002c0003t0001g0047a0002c0003t0001g0057others(66): Show | 70 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(67): Show |
intron_variant | MODIFIER | c.243+1378G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403181 | ||||||
| chr7:77403210
|
C | A | 1 | a0001c0002t0001g0280 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.243+1349G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403210 | ||||||
| chr7:77403327
|
T | C | 6 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+1232A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403327 | ||||||
| chr7:77403379
|
G | A | 2 | a0003c0004t0002g0032a0003c0004t0002g0339 | 2 | HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.243+1180C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403379 | ||||||
| chr7:77403471
|
A | T | 1 | a0002c0003t0001g0347 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.243+1088T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403471 | ||||||
| chr7:77403547
|
C | T | 3 | a0001c0001t0001g0200a0001c0010t0001g0146a0001c0010t0001g0150 | 3 | HG03139.hp2 HG03516.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.243+1012G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403547 | ||||||
| chr7:77403569
|
G | GA | 71 | a0001c0013t0001g0219a0001c0013t0001g0222a0002c0003t0001g0037others(68): Show | 72 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(69): Show |
intron_variant | MODIFIER | c.243+989dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403569 | ||||||
| chr7:77403647
|
A | C | 47 | a0002c0003t0001g0037a0002c0003t0001g0047a0002c0003t0001g0057others(44): Show | 48 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(45): Show |
intron_variant | MODIFIER | c.243+912T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403647 | ||||||
| chr7:77403680
|
C | T | 174 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(171): Show | 176 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(173): Show |
intron_variant | MODIFIER | c.243+879G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403680 | ||||||
| chr7:77403843
|
C | A | 7 | a0002c0003t0001g0037a0002c0003t0001g0061a0002c0003t0001g0062others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.243+716G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403843 | ||||||
| chr7:77404118
|
C | A | 79 | a0001c0001t0001g0214a0001c0001t0001g0296a0001c0001t0001g0297others(76): Show | 80 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.243+441G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77404118 | ||||||
| chr7:77404148
|
T | C | 4 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(1): Show | 4 | NA18957.hp1 NA18966.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.243+411A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77404148 | ||||||
| chr7:77404180
|
T | G | 15 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(12): Show | 15 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.243+379A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77404180 | ||||||
| chr7:77404186
|
A | G | 26 | a0001c0013t0001g0219a0001c0013t0001g0222a0002c0003t0001g0064others(23): Show | 26 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.243+373T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77404186 | ||||||
| chr7:77404401
|
T | C | 1 | a0002c0003t0001g0320 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.243+158A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77404401 | ||||||
| chr7:77404478
|
G | C | 15 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(12): Show | 15 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.243+81C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77404478 | ||||||
| chr7:77404620
|
A | G | 81 | a0001c0001t0001g0214a0001c0001t0001g0296a0001c0001t0001g0297others(78): Show | 82 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
splice_region_variant&intron_variant | LOW | c.187-5T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77404620 | ||||||
| chr7:77404698
|
AACTC | A | 11 | a0001c0002t0001g0118a0001c0002t0001g0194a0001c0002t0001g0235others(8): Show | 11 | HG00597.hp1 HG00673.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.187-87_187-84delGA others(2): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77404698 | ||||||
| chr7:77404768
|
C | T | 10 | a0001c0028t0002g0143a0002c0027t0001g0215a0006c0008t0001g0016others(7): Show | 10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.187-153G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77404768 | ||||||
| chr7:77404807
|
A | C | 10 | a0001c0028t0002g0143a0002c0027t0001g0215a0006c0008t0001g0016others(7): Show | 10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.187-192T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77404807 | ||||||
| chr7:77405060
|
C | A | 15 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0020others(12): Show | 16 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.187-445G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405060 | ||||||
| chr7:77405094
|
TTATAG | T | 15 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0020others(12): Show | 16 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.187-484_187-480del others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405094 | ||||||
| chr7:77405161
|
A | C | 1 | a0001c0002t0001g0264 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.187-546T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405161 | ||||||
| chr7:77405235
|
G | C | 15 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0020others(12): Show | 16 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.187-620C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405235 | ||||||
| chr7:77405308
|
AAAT | A | 10 | a0001c0028t0002g0143a0002c0027t0001g0215a0006c0008t0001g0016others(7): Show | 10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.187-696_187-694del others(3): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405308 | ||||||
| chr7:77405346
|
G | A | 10 | a0001c0028t0002g0143a0002c0027t0001g0215a0006c0008t0001g0016others(7): Show | 10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.186+683C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405346 | ||||||
| chr7:77405364
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.186+665A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405364 | ||||||
| chr7:77405377
|
C | T | 1 | a0012c0022t0001g0130 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.186+652G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405377 | ||||||
| chr7:77405533
|
T | TA | 36 | a0001c0013t0001g0219a0001c0013t0001g0222a0001c0028t0002g0143others(33): Show | 36 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.186+495dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405533 | ||||||
| chr7:77405570
|
C | T | 2 | a0001c0002t0002g0008a0001c0002t0002g0010 | 2 | HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.186+459G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405570 | ||||||
| chr7:77405651
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0210 | 2 | HG00099.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.186+378G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405651 | ||||||
| chr7:77405847
|
C | G | 1 | a0007c0011t0002g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.186+182G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405847 | ||||||
| chr7:77405905
|
T | C | 15 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(12): Show | 15 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.186+124A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405905 | ||||||
| chr7:77406163
|
C | G | 10 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(7): Show | 10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.110-58G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406163 | ||||||
| chr7:77406331
|
C | A | 15 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(12): Show | 15 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.110-226G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406331 | ||||||
| chr7:77406332
|
G | A | 10 | a0001c0028t0002g0143a0002c0027t0001g0215a0006c0008t0001g0016others(7): Show | 10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-227C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406332 | ||||||
| chr7:77406488
|
C | T | 1 | a0002c0003t0001g0347 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.110-383G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406488 | ||||||
| chr7:77406535
|
T | G | 1 | a0001c0001t0001g0317 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.110-430A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406535 | ||||||
| chr7:77406565
|
T | C | 2 | a0001c0002t0001g0244a0001c0002t0001g0263 | 2 | HG03831.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.110-460A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406565 | ||||||
| chr7:77406597
|
A | G | 1 | a0001c0001t0001g0257 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.110-492T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406597 | ||||||
| chr7:77406661
|
G | C | 80 | a0001c0001t0001g0214a0001c0001t0001g0296a0001c0001t0001g0297others(77): Show | 81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.110-556C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406661 | ||||||
| chr7:77406695
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.110-590T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406695 | ||||||
| chr7:77406708
|
A | G | 195 | a0001c0001t0001g0214a0001c0001t0001g0296a0001c0001t0001g0297others(192): Show | 198 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.110-603T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406708 | ||||||
| chr7:77406759
|
C | A | 1 | a0006c0008t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.110-654G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406759 | ||||||
| chr7:77406965
|
G | T | 1 | a0001c0002t0001g0300 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.110-860C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406965 | ||||||
| chr7:77406984
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0069 | 2 | HG00639.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.110-879C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406984 | ||||||
| chr7:77407160
|
C | A | 10 | a0001c0028t0002g0143a0002c0027t0001g0215a0006c0008t0001g0016others(7): Show | 10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-1055G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77407160 | ||||||
| chr7:77407258
|
A | G | 50 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(47): Show | 51 | HG01099.hp1 HG01168.hp2 HG01169.hp2 others(48): Show |
intron_variant | MODIFIER | c.110-1153T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77407258 | ||||||
| chr7:77407389
|
C | G | 83 | a0001c0001t0001g0214a0001c0001t0001g0296a0001c0001t0001g0297others(80): Show | 84 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.110-1284G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77407389 | ||||||
| chr7:77407668
|
CTG | C | 6 | a0001c0001t0001g0327a0001c0001t0001g0329a0001c0001t0001g0330others(3): Show | 6 | HG00597.hp2 HG02015.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.110-1565_110-1564d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77407668 | ||||||
| chr7:77407913
|
G | T | 1 | a0001c0002t0001g0263 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.110-1808C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77407913 | ||||||
| chr7:77407949
|
T | C | 1 | a0002c0003t0001g0336 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.110-1844A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77407949 | ||||||
| chr7:77408047
|
G | C | 14 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(11): Show | 14 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.110-1942C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77408047 | ||||||
| chr7:77408537
|
A | G | 14 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(11): Show | 14 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.110-2432T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77408537 | ||||||
| chr7:77408689
|
C | CA | 32 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(29): Show | 33 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.110-2585dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77408689 | ||||||
| chr7:77408689
|
C | CAAAAA | 10 | a0001c0002t0002g0008a0001c0002t0002g0010a0001c0002t0002g0011others(7): Show | 10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.110-2589_110-2585d others(7): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77408689 | ||||||
| chr7:77408689
|
CA | C | 79 | a0001c0001t0001g0327a0001c0001t0003g0294a0001c0002t0001g0019others(76): Show | 80 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.110-2585delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77408689 | ||||||
| chr7:77408689
|
CAA | C | 67 | a0001c0002t0001g0117a0001c0002t0001g0263a0001c0002t0002g0136others(64): Show | 68 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.110-2586_110-2585d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77408689 | ||||||
| chr7:77408689
|
CAAA | C | 6 | a0003c0004t0002g0133a0003c0004t0002g0184a0003c0004t0002g0185others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.110-2587_110-2585d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77408689 | ||||||
| chr7:77408877
|
A | G | 1 | a0009c0026t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.110-2772T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77408877 | ||||||
| chr7:77408897
|
G | A | 2 | a0001c0002t0001g0284a0013c0025t0001g0307 | 2 | HG01099.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.110-2792C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77408897 | ||||||
| chr7:77408946
|
AG | A | 14 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(11): Show | 14 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.110-2842delC | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77408946 | ||||||
| chr7:77409332
|
G | T | 59 | a0001c0001t0001g0055a0001c0001t0001g0069a0001c0028t0002g0143others(56): Show | 60 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.110-3227C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77409332 | ||||||
| chr7:77409628
|
C | T | 293 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(290): Show | 296 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.110-3523G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77409628 | ||||||
| chr7:77409713
|
C | T | 2 | a0001c0002t0001g0262a0001c0002t0001g0299 | 2 | NA18960.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.110-3608G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77409713 | ||||||
| chr7:77409741
|
G | T | 14 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(11): Show | 14 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.110-3636C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77409741 | ||||||
| chr7:77409928
|
G | C | 1 | a0012c0022t0001g0130 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.110-3823C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77409928 | ||||||
| chr7:77410092
|
A | C | 1 | a0001c0002t0001g0298 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.110-3987T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77410092 | ||||||
| chr7:77410119
|
G | A | 15 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0020others(12): Show | 16 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.110-4014C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77410119 | ||||||
| chr7:77410166
|
T | G | 79 | a0001c0001t0001g0214a0001c0001t0001g0296a0001c0001t0001g0297others(76): Show | 80 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.110-4061A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77410166 | ||||||
| chr7:77410585
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.110-4480G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77410585 | ||||||
| chr7:77410879
|
T | C | 1 | a0002c0003t0002g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.110-4774A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77410879 | ||||||
| chr7:77411037
|
G | A | 15 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(12): Show | 15 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.110-4932C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411037 | ||||||
| chr7:77411098
|
T | TA | 10 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0208others(7): Show | 11 | HG01516.hp2 HG01884.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.110-4994dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411098 | ||||||
| chr7:77411098
|
T | TAA | 45 | a0001c0001t0001g0115a0001c0001t0001g0205a0001c0002t0002g0009others(42): Show | 46 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.110-4995_110-4994d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411098 | ||||||
| chr7:77411098
|
TA | T | 221 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(218): Show | 223 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.110-4994delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411098 | ||||||
| chr7:77411098
|
TAA | T | 6 | a0001c0001t0001g0035a0001c0001t0001g0199a0001c0001t0001g0210others(3): Show | 6 | HG01070.hp1 HG01070.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.110-4995_110-4994d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411098 | ||||||
| chr7:77411230
|
C | A | 7 | a0002c0003t0001g0047a0002c0003t0001g0088a0002c0003t0001g0089others(4): Show | 7 | NA18940.hp1 NA18959.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.109+4983G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411230 | ||||||
| chr7:77411471
|
T | C | 1 | a0001c0002t0006g0006 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.109+4742A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411471 | ||||||
| chr7:77411511
|
G | A | 4 | a0007c0011t0002g0139a0007c0011t0002g0145a0007c0011t0002g0209others(1): Show | 4 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+4702C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411511 | ||||||
| chr7:77411620
|
CTAAA | C | 3 | a0001c0002t0002g0126a0001c0002t0002g0131a0002c0019t0001g0127 | 3 | HG01192.hp2 HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.109+4589_109+4592d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411620 | ||||||
| chr7:77411668
|
A | G | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.109+4545T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411668 | ||||||
| chr7:77411703
|
T | C | 1 | a0001c0001t0001g0295 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.109+4510A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411703 | ||||||
| chr7:77411770
|
A | AAT | 25 | a0001c0001t0001g0115a0001c0013t0001g0219a0001c0013t0001g0222others(22): Show | 25 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.109+4441_109+4442d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411770 | ||||||
| chr7:77411954
|
C | G | 15 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(12): Show | 15 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.109+4259G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411954 | ||||||
| chr7:77411955
|
G | A | 1 | a0001c0002t0002g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.109+4258C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411955 | ||||||
| chr7:77411970
|
A | G | 15 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(12): Show | 15 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.109+4243T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411970 | ||||||
| chr7:77411973
|
G | A | 241 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(238): Show | 244 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.109+4240C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411973 | ||||||
| chr7:77412039
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0210 | 2 | HG00099.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.109+4174G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412039 | ||||||
| chr7:77412055
|
C | T | 1 | a0003c0009t0001g0192 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.109+4158G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412055 | ||||||
| chr7:77412406
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0048a0001c0001t0001g0092others(1): Show | 4 | NA18945.hp2 NA18967.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+3807C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412406 | ||||||
| chr7:77412480
|
A | T | 4 | a0007c0011t0002g0139a0007c0011t0002g0145a0007c0011t0002g0209others(1): Show | 4 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+3733T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412480 | ||||||
| chr7:77412486
|
T | C | 162 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(159): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.109+3727A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412486 | ||||||
| chr7:77412543
|
G | C | 12 | a0001c0028t0002g0143a0002c0003t0001g0216a0002c0003t0001g0217others(9): Show | 12 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+3670C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412543 | ||||||
| chr7:77412604
|
A | G | 4 | a0001c0010t0001g0146a0001c0010t0001g0150a0001c0010t0001g0151others(1): Show | 4 | HG03139.hp2 HG03516.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+3609T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412604 | ||||||
| chr7:77412759
|
T | C | 2 | a0004c0005t0003g0163a0004c0005t0003g0164 | 2 | NA18962.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.109+3454A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412759 | ||||||
| chr7:77412760
|
A | C | 2 | a0004c0005t0003g0163a0004c0005t0003g0164 | 2 | NA18962.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.109+3453T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412760 | ||||||
| chr7:77412776
|
CA | C | 263 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(260): Show | 266 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.109+3436delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412776 | ||||||
| chr7:77412883
|
A | G | 1 | a0001c0002t0001g0144 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.109+3330T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412883 | ||||||
| chr7:77413123
|
C | G | 15 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0020others(12): Show | 16 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.109+3090G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413123 | ||||||
| chr7:77413209
|
C | T | 10 | a0001c0028t0002g0143a0002c0027t0001g0215a0006c0008t0001g0016others(7): Show | 10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+3004G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413209 | ||||||
| chr7:77413231
|
G | A | 15 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(12): Show | 15 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.109+2982C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413231 | ||||||
| chr7:77413268
|
A | G | 1 | a0002c0003t0001g0121 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.109+2945T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413268 | ||||||
| chr7:77413283
|
T | C | 1 | a0001c0001t0001g0096 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.109+2930A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413283 | ||||||
| chr7:77413314
|
C | T | 79 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(76): Show | 80 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.109+2899G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413314 | ||||||
| chr7:77413406
|
A | G | 1 | a0002c0003t0001g0029 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.109+2807T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413406 | ||||||
| chr7:77413597
|
G | A | 5 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0097others(2): Show | 5 | HG02074.hp1 NA18948.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+2616C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413597 | ||||||
| chr7:77413839
|
C | T | 10 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(7): Show | 10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.109+2374G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413839 | ||||||
| chr7:77413845
|
T | A | 2 | a0001c0002t0002g0136a0001c0002t0002g0141 | 2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.109+2368A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413845 | ||||||
| chr7:77413857
|
G | GT | 162 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(159): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.109+2355dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413857 | ||||||
| chr7:77413857
|
G | GTT | 29 | a0001c0001t0001g0034a0001c0001t0001g0205a0001c0002t0002g0008others(26): Show | 30 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.109+2354_109+2355d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413857 | ||||||
| chr7:77413857
|
G | GTTT | 96 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0305others(93): Show | 97 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.109+2353_109+2355d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413857 | ||||||
| chr7:77413857
|
G | GTTTT | 22 | a0001c0001t0001g0115a0001c0002t0001g0052a0001c0013t0001g0219others(19): Show | 22 | HG00140.hp1 HG01361.hp1 HG01993.hp1 others(19): Show |
intron_variant | MODIFIER | c.109+2352_109+2355d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413857 | ||||||
| chr7:77413857
|
G | T | 1 | a0001c0001t0001g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.109+2356C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413857 | ||||||
| chr7:77413865
|
C | T | 180 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(177): Show | 182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.109+2348G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413865 | ||||||
| chr7:77414069
|
T | A | 81 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0002t0001g0019others(78): Show | 82 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.109+2144A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414069 | ||||||
| chr7:77414227
|
A | C | 2 | a0003c0004t0002g0153a0003c0004t0002g0154 | 2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.109+1986T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414227 | ||||||
| chr7:77414250
|
A | T | 1 | a0003c0004t0002g0147 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.109+1963T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414250 | ||||||
| chr7:77414546
|
A | G | 195 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0030others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.109+1667T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414546 | ||||||
| chr7:77414772
|
T | C | 1 | a0001c0028t0002g0143 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.109+1441A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414772 | ||||||
| chr7:77414844
|
C | CTTTTT | 8 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.109+1364_109+1368d others(7): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
C | CTTTTTT | 40 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0021others(37): Show | 41 | HG00140.hp2 HG00609.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.109+1363_109+1368d others(8): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
C | CTTTTTTT | 50 | a0001c0001t0001g0017a0001c0001t0001g0195a0001c0001t0001g0196others(47): Show | 50 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.109+1362_109+1368d others(9): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
C | CTTTTTTT others(1): Show |
14 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0002t0001g0194others(11): Show | 14 | HG00544.hp2 HG00621.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.109+1361_109+1368d others(10): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
C | CTTTTTTT others(2): Show |
6 | a0001c0001t0001g0014a0001c0001t0001g0232a0001c0002t0001g0233others(3): Show | 6 | HG00639.hp1 HG02630.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.109+1360_109+1368d others(11): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
C | CTTTTTTT others(3): Show |
1 | a0001c0002t0002g0141 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.109+1359_109+1368d others(12): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
C | CTTTTTTT others(5): Show |
3 | a0001c0002t0001g0231a0006c0008t0001g0140a0007c0011t0002g0139 | 3 | HG02165.hp2 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.109+1357_109+1368d others(14): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
C | CTTTTTTT others(6): Show |
2 | a0006c0008t0001g0137a0006c0008t0001g0138 | 2 | HG01074.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.109+1356_109+1368d others(15): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
C | CTTTTTTT others(7): Show |
3 | a0001c0002t0002g0136a0003c0004t0001g0191a0006c0008t0001g0016 | 3 | HG02523.hp2 HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.109+1355_109+1368d others(16): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
C | CTTTTTTT others(8): Show |
1 | a0006c0008t0001g0135 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.109+1354_109+1368d others(17): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
C | CTTTTTTT others(12): Show |
1 | a0003c0009t0001g0190 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.109+1350_109+1368d others(21): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
C | CTTTTTTT others(13): Show |
1 | a0003c0009t0001g0189 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.109+1349_109+1368d others(22): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
CTT | C | 6 | a0001c0010t0001g0150a0001c0010t0001g0151a0001c0010t0001g0152others(3): Show | 6 | HG02683.hp1 HG03098.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+1367_109+1368d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
CTTT | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0002t0004g0033others(3): Show | 6 | HG00423.hp2 HG01243.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+1366_109+1368d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
CTTTT | C | 25 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0039others(22): Show | 25 | HG00408.hp2 HG00735.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.109+1365_109+1368d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
CTTTTT | C | 108 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0056others(105): Show | 110 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.109+1364_109+1368d others(7): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
CTTTTTT | C | 11 | a0001c0002t0001g0346a0001c0002t0002g0126a0001c0013t0001g0222others(8): Show | 11 | HG00140.hp1 HG00733.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.109+1363_109+1368d others(8): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
CTTTTTTT | C | 10 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(7): Show | 10 | HG01192.hp2 HG01433.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.109+1362_109+1368d others(9): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
CTTTTTTT others(3): Show |
C | 1 | a0003c0004t0002g0157 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.109+1359_109+1368d others(12): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
CTTTTTTT others(4): Show |
C | 29 | a0001c0002t0001g0158a0001c0002t0002g0183a0004c0005t0001g0172others(26): Show | 29 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.109+1358_109+1368d others(13): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
CTTTTTTT others(5): Show |
C | 1 | a0002c0003t0001g0225 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.109+1357_109+1368d others(14): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
CTTTTTTT others(6): Show |
C | 7 | a0001c0001t0001g0226a0003c0004t0002g0133a0003c0004t0002g0184others(4): Show | 7 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.109+1356_109+1368d others(15): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414844
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.109+1354_109+1368d others(17): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | ||||||
| chr7:77414903
|
G | C | 4 | a0003c0004t0001g0191a0003c0009t0001g0189a0003c0009t0001g0190others(1): Show | 4 | HG02523.hp2 NA18939.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+1310C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414903 | ||||||
| chr7:77414904
|
C | T | 3 | a0002c0007t0001g0228a0002c0007t0001g0229a0002c0007t0001g0230 | 3 | NA18978.hp2 NA18983.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.109+1309G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414904 | ||||||
| chr7:77415019
|
A | G | 1 | a0003c0004t0002g0134 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.109+1194T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415019 | ||||||
| chr7:77415117
|
C | T | 2 | a0001c0001t0001g0014a0001c0010t0001g0015 | 2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.109+1096G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415117 | ||||||
| chr7:77415131
|
A | G | 164 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0017others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.109+1082T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415131 | ||||||
| chr7:77415137
|
C | T | 6 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+1076G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415137 | ||||||
| chr7:77415221
|
A | T | 1 | a0001c0001t0001g0193 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.109+992T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415221 | ||||||
| chr7:77415447
|
T | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(148): Show | 153 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.109+766A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415447 | ||||||
| chr7:77415515
|
C | T | 1 | a0001c0001t0001g0007 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.109+698G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415515 | ||||||
| chr7:77415603
|
G | A | 1 | a0003c0004t0002g0339 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.109+610C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415603 | ||||||
| chr7:77415675
|
C | T | 1 | a0001c0002t0006g0006 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.109+538G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415675 | ||||||
| chr7:77415675
|
CCT | C | 4 | a0002c0003t0001g0004a0003c0004t0002g0340a0003c0004t0002g0341others(1): Show | 5 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+536_109+537del others(2): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415675 | ||||||
| chr7:77415854
|
G | C | 4 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(1): Show | 4 | HG01099.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+359C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415854 | ||||||
| chr7:77416055
|
A | G | 1 | a0001c0001t0001g0005 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.109+158T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77416055 | ||||||
| chr7:77416160
|
T | G | 1 | a0002c0003t0001g0347 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.109+53A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77416160 | ||||||
| chr7:77416195
|
G | A | 1 | a0014c0017t0001g0348 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.109+18C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77416195 |