Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 116988 |
|---|---|
| ensemblid | ENSG00000133612.20 |
| hgncid | 16923 |
| symbol | AGAP3 |
| name | ArfGAP with GTPase domain, ankyrin repeat and PH domain 3 |
| refseq_nuc | NM_031946.7 |
| refseq_prot | NP_114152.3 |
| ensembl_nuc | ENST00000397238.7 |
| ensembl_prot | ENSP00000380413.2 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 151086475 |
| end | 151144434 |
| strand | + |
| ver | v1.2 |
| region | chr7:151086475-151144434 |
| region5000 | chr7:151081475-151149434 |
| regionname0 | AGAP3_chr7_151086475_151144434 |
| regionname5000 | AGAP3_chr7_151081475_151149434 |
| 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 | 912 | 347 | 93 | 64 | 137 | 15 | 37 | 98 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0002 | 1/0 | 911 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0003 | 0/0 | 266 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0004 | 0/0 | 912 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0005 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0006 | 0/0 | 912 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0007 | 0/0 | 912 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0008 | 0/0 | 912 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| 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 | 2739 | 316 | 68 | 61 | 135 | 15 | 36 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| c0002 | 0/0 | 2739 | 8 | 8 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| c0003 | 0/0 | 2739 | 6 | 6 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| c0004 | 0/0 | 2739 | 4 | 4 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| c0005 | 0/0 | 2739 | 3 | 3 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| c0006 | 0/0 | 2739 | 2 | 0 | 2 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| c0007 | 0/0 | 2739 | 2 | 2 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| c0008 | 1/0 | 2736 | 1 | 0 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| c0009 | 0/0 | 2739 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| c0010 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| c0011 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| c0012 | 0/0 | 2739 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| c0013 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| c0014 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| c0015 | 0/0 | 2739 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| c0016 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| c0017 | 0/0 | 2739 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| c0018 | 0/0 | 2739 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| c0019 | 0/0 | 2762 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| c0020 | 0/0 | 2739 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| 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 | 0/0 | 756 | 235 | 45 | 49 | 102 | 12 | 27 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| t0002 | 0/1 | 753 | 79 | 31 | 13 | 22 | 2 | 10 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| t0003 | 0/0 | 756 | 12 | 12 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| t0004 | 1/0 | 759 | 9 | 0 | 2 | 3 | 2 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| t0005 | 0/0 | 753 | 8 | 0 | 0 | 8 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| t0006 | 0/0 | 759 | 6 | 6 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| t0007 | 0/0 | 753 | 3 | 0 | 0 | 3 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| t0008 | 0/0 | 756 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| t0009 | 0/0 | 756 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| 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 | 4 | 0 | 2 | 2 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0322 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| 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 | 2739 | 316 | 68 | 61 | 135 | 15 | 36 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0002 | 0/0 | 2739 | 8 | 8 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0003 | 0/0 | 2739 | 6 | 6 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0004 | 0/0 | 2739 | 4 | 4 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0005 | 0/0 | 2739 | 3 | 3 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0006 | 0/0 | 2739 | 2 | 0 | 2 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0007 | 0/0 | 2739 | 2 | 2 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0009 | 0/0 | 2739 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0011 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0013 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0017 | 0/0 | 2739 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0018 | 0/0 | 2739 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0020 | 0/0 | 2739 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0002c0008 | 1/0 | 2736 | 1 | 0 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0003c0019 | 0/0 | 2762 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0004c0016 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0005c0012 | 0/0 | 2739 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0006c0015 | 0/0 | 2739 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0007c0014 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0008c0010 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3494 | 215 | 35 | 46 | 97 | 11 | 26 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0001t0002 | 0/1 | 3491 | 67 | 19 | 13 | 22 | 2 | 10 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0001t0003 | 0/0 | 3494 | 12 | 12 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0001t0004 | 0/0 | 3497 | 7 | 0 | 2 | 3 | 2 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0001t0005 | 0/0 | 3491 | 8 | 0 | 0 | 8 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0001t0006 | 0/0 | 3497 | 2 | 2 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0001t0007 | 0/0 | 3491 | 3 | 0 | 0 | 3 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0001t0008 | 0/0 | 3494 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0001t0009 | 0/0 | 3494 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0002t0002 | 0/0 | 3491 | 8 | 8 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0003t0001 | 0/0 | 3494 | 5 | 5 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0003t0006 | 0/0 | 3497 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0004t0001 | 0/0 | 3494 | 4 | 4 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0005t0006 | 0/0 | 3497 | 3 | 3 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0006t0001 | 0/0 | 3494 | 2 | 0 | 2 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0007t0002 | 0/0 | 3491 | 2 | 2 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0009t0001 | 0/0 | 3494 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0011t0001 | 0/0 | 3494 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0013t0001 | 0/0 | 3494 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0017t0001 | 0/0 | 3494 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0018t0001 | 0/0 | 3494 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0001c0020t0002 | 0/0 | 3491 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0002c0008t0004 | 1/0 | 3494 | 1 | 0 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0003c0019t0004 | 0/0 | 3520 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0004c0016t0001 | 0/0 | 3494 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0005c0012t0002 | 0/0 | 3491 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0006c0015t0001 | 0/0 | 3494 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0007c0014t0001 | 0/0 | 3494 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| a0008c0010t0001 | 0/0 | 3494 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | copy fasta | chr7 | 151081475 | 151149434 |
| 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 | 0 | 0 | 2 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0322 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0004g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0005g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0006g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0006g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0007g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0007g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0007g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0008g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0009g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0002t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0002t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0002t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0002t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0002t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0002t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0002t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0002t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0003t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0003t0006g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0004t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0004t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0004t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0004t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0005t0006g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0005t0006g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0005t0006g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0006t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0006t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0007t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0007t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0009t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0011t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0013t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0017t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0018t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0020t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0002c0008t0004g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0003c0019t0004g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0004c0016t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0005c0012t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0006c0015t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0007c0014t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0008c0010t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0342 | EUR | GBR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00140 | hp1 | a0006 | c0015 | t0001 | g0124 | EUR | GBR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | FIN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0296 | EUR | FIN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | FIN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0329 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0221 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01081 | hp1 | a0001 | c0006 | t0001 | g0019 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0323 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0324 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01109 | hp2 | a0001 | c0006 | t0001 | g0042 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0294 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01255 | hp2 | a0001 | c0009 | t0001 | g0068 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0253 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0273 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0344 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0327 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0343 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0304 | EUR | IBS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | IBS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | IBS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0270 | EUR | IBS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | IBS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0311 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01891 | hp1 | a0001 | c0020 | t0002 | g0315 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0341 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0306 | AMR | PEL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0168 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02056 | hp1 | a0001 | c0013 | t0001 | g0213 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02071 | hp2 | a0007 | c0014 | t0001 | g0033 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0252 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02257 | hp2 | a0001 | c0005 | t0006 | g0339 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0137 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0317 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02280 | hp2 | a0001 | c0018 | t0001 | g0108 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0337 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02572 | hp1 | a0001 | c0005 | t0006 | g0338 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0297 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0332 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0135 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0313 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02723 | hp1 | a0001 | c0007 | t0002 | g0320 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0326 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0299 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0314 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0321 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02922 | hp1 | a0001 | c0003 | t0006 | g0340 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0208 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02970 | hp1 | a0001 | c0004 | t0001 | g0014 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0319 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02976 | hp2 | a0001 | c0005 | t0006 | g0336 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0303 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0248 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0312 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0330 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0281 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0251 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0335 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0328 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0276 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0310 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0132 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0318 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0134 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0295 | SAS | BEB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03831 | hp2 | a0003 | c0019 | t0004 | g0292 | SAS | BEB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03834 | hp1 | a0001 | c0017 | t0001 | g0222 | SAS | BEB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0325 | SAS | BEB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | STU | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0305 | SAS | STU | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | BEB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | STU | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18522 | hp1 | a0005 | c0012 | t0002 | g0334 | AFR | YRI | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | YRI | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | YRI | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | YRI | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0153 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18942 | hp2 | a0001 | c0001 | t0008 | g0022 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18961 | hp2 | a0001 | c0001 | t0005 | g0141 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18967 | hp2 | a0001 | c0001 | t0007 | g0156 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18974 | hp2 | a0001 | c0001 | t0005 | g0126 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0170 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18986 | hp1 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19011 | hp2 | a0008 | c0010 | t0001 | g0244 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0027 | AFR | LWK | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0016 | AFR | LWK | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0190 | AFR | LWK | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19065 | hp1 | a0001 | c0001 | t0007 | g0152 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19065 | hp2 | a0004 | c0016 | t0001 | g0052 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19081 | hp1 | a0001 | c0001 | t0007 | g0172 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19083 | hp2 | a0001 | c0011 | t0001 | g0219 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0142 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19090 | hp1 | a0001 | c0001 | t0009 | g0204 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0171 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | YRI | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19240 | hp2 | a0001 | c0004 | t0001 | g0013 | AFR | YRI | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0333 | AFR | ASW | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ASW | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | TSI | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0271 | EUR | TSI | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | GIH | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0307 | SAS | GIH | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0298 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0209 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG06807 | hp1 | a0001 | c0007 | t0002 | g0316 | AFR | USA | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | USA | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0322 | REF | REF | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| homoSapiens_grch38 | hp1 | a0002 | c0008 | t0004 | g0272 | REF | REF | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:151086812
|
G | GT | 1 | a0001 | 9 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
frameshift_variant | HIGH | c.71_72insT | p.Ala25fs | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | 339/3494 | 72/2736 | 24/911 | chr7 | 151086812 | ||
| chr7:151086813
|
C | CG | 7 | a0001a0003a0004others(4): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
frameshift_variant | HIGH | c.73dupG | p.Ala25fs | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | 341/3494 | 74/2736 | 25/911 | INFO_REALIGN_3_PRIME | chr7 | 151086813 | |
| chr7:151086821
|
C | CG | 7 | a0001a0003a0004others(4): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
frameshift_variant | HIGH | c.81dupG | p.Gln28fs | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | 349/3494 | 82/2736 | 28/911 | INFO_REALIGN_3_PRIME | chr7 | 151086821 | |
| chr7:151086824
|
A | G | 7 | a0001a0003a0004others(4): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
missense_variant | MODERATE | c.83A>G | p.Gln28Arg | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | 350/3494 | 83/2736 | 28/911 | chr7 | 151086824 | ||
| chr7:151086830
|
T | G | 7 | a0001a0003a0004others(4): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
missense_variant | MODERATE | c.89T>G | p.Leu30Arg | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | 356/3494 | 89/2736 | 30/911 | chr7 | 151086830 | ||
| chr7:151086831
|
C | CG | 7 | a0001a0003a0004others(4): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
frameshift_variant | HIGH | c.91dupG | p.Val31fs | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | 359/3494 | 92/2736 | 31/911 | INFO_REALIGN_3_PRIME | chr7 | 151086831 | |
| chr7:151086833
|
T | G | 7 | a0001a0003a0004others(4): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
missense_variant | MODERATE | c.92T>G | p.Val31Gly | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | 359/3494 | 92/2736 | 31/911 | chr7 | 151086833 | ||
| chr7:151086835
|
T | G | 7 | a0001a0003a0004others(4): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
missense_variant | MODERATE | c.94T>G | p.Cys32Gly | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | 361/3494 | 94/2736 | 32/911 | chr7 | 151086835 | ||
| chr7:151117643
|
C | CTGGGCGT others(6): Show |
1 | a0003 | 1 | HG03831.hp2 | frameshift_variant | HIGH | c.572_573insTGGGCGTG others(5): Show |
p.Trp192fs | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/18 | 840/3494 | 573/2736 | 191/911 | chr7 | 151117643 | ||
| chr7:151117645
|
T | TTGTTGGT others(3): Show |
1 | a0003 | 1 | HG03831.hp2 | frameshift_variant | HIGH | c.574_575insTGTTGGTT others(2): Show |
p.Trp192fs | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/18 | 842/3494 | 575/2736 | 192/911 | chr7 | 151117645 | ||
| chr7:151117652
|
A | C | 1 | a0003 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.581A>C | p.Asp194Ala | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/18 | 848/3494 | 581/2736 | 194/911 | chr7 | 151117652 | ||
| chr7:151117661
|
T | A | 1 | a0003 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.590T>A | p.Val197Glu | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/18 | 857/3494 | 590/2736 | 197/911 | chr7 | 151117661 | ||
| chr7:151117669
|
T | G | 1 | a0003 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.598T>G | p.Phe200Val | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/18 | 865/3494 | 598/2736 | 200/911 | chr7 | 151117669 | ||
| chr7:151117686
|
A | C | 1 | a0003 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.615A>C | p.Glu205Asp | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/18 | 882/3494 | 615/2736 | 205/911 | chr7 | 151117686 | ||
| chr7:151118624
|
A | T | 1 | a0004 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.961A>T | p.Ile321Phe | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/18 | 1228/3494 | 961/2736 | 321/911 | chr7 | 151118624 | ||
| chr7:151119999
|
G | A | 1 | a0008 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.982G>A | p.Gly328Ser | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/18 | 1249/3494 | 982/2736 | 328/911 | chr7 | 151119999 | ||
| chr7:151138250
|
G | A | 1 | a0005 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.1603G>A | p.Val535Ile | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/18 | 1870/3494 | 1603/2736 | 535/911 | chr7 | 151138250 | ||
| chr7:151143353
|
A | T | 1 | a0006 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.2286A>T | p.Glu762Asp | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 17/18 | 2553/3494 | 2286/2736 | 762/911 | chr7 | 151143353 | ||
| chr7:151143924
|
G | A | 1 | a0007 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.2717G>A | p.Arg906His | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 18/18 | 2984/3494 | 2717/2736 | 906/911 | chr7 | 151143924 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:151086813
|
C | G | 2 | a0001c0002a0001c0020 | 9 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
synonymous_variant | LOW | c.72C>G | p.Gly24Gly | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | 339/3494 | 72/2736 | 24/911 | chr7 | 151086813 | ||
| chr7:151086816
|
T | G | 19 | a0001c0001a0001c0002a0001c0003others(16): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
synonymous_variant | LOW | c.75T>G | p.Ala25Ala | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | 342/3494 | 75/2736 | 25/911 | chr7 | 151086816 | ||
| chr7:151086819
|
C | G | 19 | a0001c0001a0001c0002a0001c0003others(16): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
synonymous_variant | LOW | c.78C>G | p.Ala26Ala | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | 345/3494 | 78/2736 | 26/911 | chr7 | 151086819 | ||
| chr7:151086834
|
C | G | 19 | a0001c0001a0001c0002a0001c0003others(16): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
synonymous_variant | LOW | c.93C>G | p.Val31Val | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | 360/3494 | 93/2736 | 31/911 | chr7 | 151086834 | ||
| chr7:151117656
|
A | T | 1 | a0003c0019 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.585A>T | p.Ala195Ala | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/18 | 852/3494 | 585/2736 | 195/911 | chr7 | 151117656 | ||
| chr7:151117717
|
C | T | 1 | a0001c0007 | 2 | HG02723.hp1 HG06807.hp1 |
synonymous_variant | LOW | c.646C>T | p.Leu216Leu | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/18 | 913/3494 | 646/2736 | 216/911 | chr7 | 151117717 | ||
| chr7:151118259
|
C | T | 2 | a0001c0002a0001c0004 | 12 | HG01884.hp2 HG02280.hp1 HG02886.hp1 others(9): Show |
synonymous_variant | LOW | c.756C>T | p.Arg252Arg | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 6/18 | 1023/3494 | 756/2736 | 252/911 | chr7 | 151118259 | ||
| chr7:151118543
|
C | T | 2 | a0001c0003a0001c0018 | 7 | HG02055.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
synonymous_variant | LOW | c.880C>T | p.Leu294Leu | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/18 | 1147/3494 | 880/2736 | 294/911 | chr7 | 151118543 | ||
| chr7:151118593
|
C | T | 1 | a0001c0017 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.930C>T | p.Ala310Ala | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/18 | 1197/3494 | 930/2736 | 310/911 | chr7 | 151118593 | ||
| chr7:151118614
|
G | A | 1 | a0001c0009 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.951G>A | p.Pro317Pro | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/18 | 1218/3494 | 951/2736 | 317/911 | chr7 | 151118614 | ||
| chr7:151123838
|
G | A | 1 | a0001c0011 | 1 | NA19083.hp2 | synonymous_variant | LOW | c.1173G>A | p.Glu391Glu | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/18 | 1440/3494 | 1173/2736 | 391/911 | chr7 | 151123838 | ||
| chr7:151123850
|
C | T | 1 | a0001c0006 | 2 | HG01081.hp1 HG01109.hp2 |
synonymous_variant | LOW | c.1185C>T | p.Asp395Asp | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/18 | 1452/3494 | 1185/2736 | 395/911 | chr7 | 151123850 | ||
| chr7:151134553
|
C | T | 2 | a0001c0005a0001c0018 | 4 | HG02257.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
synonymous_variant | LOW | c.1480C>T | p.Leu494Leu | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/18 | 1747/3494 | 1480/2736 | 494/911 | chr7 | 151134553 | ||
| chr7:151141911
|
G | A | 1 | a0005c0012 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.1818G>A | p.Ser606Ser | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 14/18 | 2085/3494 | 1818/2736 | 606/911 | chr7 | 151141911 | ||
| chr7:151142437
|
G | C | 1 | a0001c0013 | 1 | HG02056.hp1 | synonymous_variant | LOW | c.2076G>C | p.Leu692Leu | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 16/18 | 2343/3494 | 2076/2736 | 692/911 | chr7 | 151142437 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:151086523
|
G | T | 1 | a0001c0001t0009 | 1 | NA19090.hp1 | 5_prime_UTR_variant | MODIFIER | c.-219G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | 219 | chr7 | 151086523 | |||||
| chr7:151086669
|
TGCC | T | 16 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(13): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
5_prime_UTR_variant | MODIFIER | c.-51_-49delGCC | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | 49 | INFO_REALIGN_3_PRIME | chr7 | 151086669 | ||||
| chr7:151086669
|
TGCCGCC | T | 7 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(4): Show | 90 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(87): Show |
5_prime_UTR_variant | MODIFIER | c.-54_-49delGCCGCC | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | 49 | INFO_REALIGN_3_PRIME | chr7 | 151086669 | ||||
| chr7:151086675
|
C | T | 3 | a0001c0001t0006a0001c0003t0006a0001c0005t0006 | 6 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-67C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | chr7 | 151086675 | ||||||
| chr7:151144095
|
C | T | 1 | a0001c0001t0007 | 3 | NA18967.hp2 NA19065.hp1 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*152C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 18/18 | 152 | chr7 | 151144095 | |||||
| chr7:151144231
|
A | G | 1 | a0001c0001t0003 | 12 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*288A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 18/18 | 288 | chr7 | 151144231 | |||||
| chr7:151144291
|
G | A | 3 | a0001c0001t0005a0001c0001t0007a0001c0001t0008 | 12 | NA18941.hp1 NA18942.hp2 NA18961.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*348G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 18/18 | 348 | chr7 | 151144291 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:151087173
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0009 | 3 | HG00140.hp2 HG01175.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.331+101G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087173 | ||||||
| chr7:151087175
|
T | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0009 | 3 | HG00140.hp2 HG01175.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.331+103T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087175 | ||||||
| chr7:151087176
|
C | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0009 | 3 | HG00140.hp2 HG01175.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.331+104C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087176 | ||||||
| chr7:151087178
|
T | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0009 | 3 | HG00140.hp2 HG01175.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.331+106T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087178 | ||||||
| chr7:151087180
|
GC | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0009 | 3 | HG00140.hp2 HG01175.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.331+109delC | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087180 | ||||||
| chr7:151087320
|
T | C | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(169): Show | 177 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.331+248T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087320 | ||||||
| chr7:151087321
|
T | G | 1 | a0001c0001t0001g0177 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.331+249T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087321 | ||||||
| chr7:151087367
|
G | A | 1 | a0001c0001t0002g0010 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.331+295G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087367 | ||||||
| chr7:151087426
|
C | T | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(172): Show | 180 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.331+354C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087426 | ||||||
| chr7:151087428
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.331+356G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087428 | ||||||
| chr7:151087459
|
G | A | 4 | a0001c0001t0001g0015a0001c0004t0001g0013a0001c0004t0001g0014others(1): Show | 4 | HG02723.hp2 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.331+387G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087459 | ||||||
| chr7:151087474
|
C | T | 1 | a0001c0001t0004g0342 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.331+402C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087474 | ||||||
| chr7:151087593
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.331+521G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087593 | ||||||
| chr7:151087594
|
G | T | 1 | a0001c0001t0002g0178 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.331+522G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087594 | ||||||
| chr7:151087650
|
C | A | 91 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(88): Show | 92 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.331+578C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087650 | ||||||
| chr7:151087737
|
G | T | 173 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(170): Show | 178 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.331+665G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087737 | ||||||
| chr7:151087748
|
CGCACCCG others(7): Show |
C | 9 | a0001c0001t0002g0333a0001c0001t0002g0335a0001c0001t0006g0337others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.331+678_331+691del others(14): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151087748 | |||||
| chr7:151087774
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.331+702C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087774 | ||||||
| chr7:151087843
|
G | T | 1 | a0001c0001t0002g0332 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.331+771G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087843 | ||||||
| chr7:151087925
|
G | A | 173 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(170): Show | 178 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.331+853G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087925 | ||||||
| chr7:151087967
|
C | G | 1 | a0001c0001t0001g0331 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.331+895C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087967 | ||||||
| chr7:151088061
|
G | A | 1 | a0001c0001t0003g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.331+989G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151088061 | ||||||
| chr7:151088234
|
C | T | 173 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(170): Show | 178 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.331+1162C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151088234 | ||||||
| chr7:151088393
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0004t0001g0013others(3): Show | 6 | HG02280.hp2 HG02723.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.331+1321G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151088393 | ||||||
| chr7:151088530
|
C | G | 1 | a0001c0018t0001g0108 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.331+1458C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151088530 | ||||||
| chr7:151088666
|
C | T | 51 | a0001c0001t0002g0178a0001c0001t0002g0293a0001c0001t0002g0294others(48): Show | 51 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.331+1594C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151088666 | ||||||
| chr7:151088697
|
G | A | 1 | a0001c0001t0002g0109 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.331+1625G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151088697 | ||||||
| chr7:151088825
|
T | A | 1 | a0001c0001t0001g0179 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.331+1753T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151088825 | ||||||
| chr7:151088964
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.331+1892C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151088964 | ||||||
| chr7:151088974
|
C | T | 127 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(124): Show | 131 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.331+1902C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151088974 | ||||||
| chr7:151088996
|
G | T | 1 | a0001c0001t0001g0176 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.331+1924G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151088996 | ||||||
| chr7:151089064
|
G | C | 2 | a0001c0004t0001g0013a0001c0004t0001g0014 | 2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.331+1992G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151089064 | ||||||
| chr7:151089163
|
A | G | 6 | a0001c0001t0006g0337a0001c0001t0006g0341a0001c0003t0006g0340others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.331+2091A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151089163 | ||||||
| chr7:151089164
|
G | GA | 10 | a0001c0001t0001g0004a0001c0001t0001g0116a0001c0001t0001g0117others(7): Show | 11 | HG00140.hp1 HG00639.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.331+2102dupA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151089164 | |||||
| chr7:151089296
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.331+2224A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151089296 | ||||||
| chr7:151089315
|
G | T | 1 | a0001c0001t0002g0330 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.331+2243G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151089315 | ||||||
| chr7:151089341
|
C | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG01496.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.331+2269C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151089341 | ||||||
| chr7:151089474
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.331+2402G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151089474 | ||||||
| chr7:151089549
|
G | A | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(1): Show | 4 | HG02486.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.331+2477G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151089549 | ||||||
| chr7:151089802
|
CA | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(98): Show | 102 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.331+2731delA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151089802 | ||||||
| chr7:151089959
|
G | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(98): Show | 102 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.331+2887G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151089959 | ||||||
| chr7:151090154
|
C | T | 1 | a0001c0001t0002g0329 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.331+3082C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090154 | ||||||
| chr7:151090236
|
T | TG | 18 | a0001c0001t0001g0179a0001c0001t0001g0282a0001c0001t0001g0283others(15): Show | 18 | HG00597.hp2 HG01099.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.331+3176dupG | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151090236 | |||||
| chr7:151090236
|
TG | T | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(167): Show | 175 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.331+3176delG | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151090236 | |||||
| chr7:151090239
|
G | C | 3 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0002g0295 | 3 | HG01167.hp1 HG01169.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.331+3167G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090239 | ||||||
| chr7:151090240
|
G | C | 1 | a0001c0001t0003g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.331+3168G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090240 | ||||||
| chr7:151090240
|
G | T | 1 | a0001c0004t0001g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.331+3168G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090240 | ||||||
| chr7:151090310
|
A | G | 15 | a0001c0001t0002g0178a0001c0001t0002g0313a0001c0001t0002g0322others(12): Show | 15 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.331+3238A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090310 | ||||||
| chr7:151090363
|
T | G | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(172): Show | 180 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.331+3291T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090363 | ||||||
| chr7:151090380
|
CT | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(108): Show | 115 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.331+3333delT | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151090380 | |||||
| chr7:151090380
|
CTT | C | 104 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(101): Show | 105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.331+3332_331+3333d others(4): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151090380 | |||||
| chr7:151090380
|
CTTT | C | 95 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0018others(92): Show | 99 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.331+3331_331+3333d others(5): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151090380 | |||||
| chr7:151090402
|
T | A | 3 | a0001c0002t0002g0310a0001c0002t0002g0311a0001c0002t0002g0312 | 3 | HG01884.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.331+3330T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090402 | ||||||
| chr7:151090405
|
T | A | 1 | a0001c0001t0001g0017 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.331+3333T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090405 | ||||||
| chr7:151090418
|
C | T | 6 | a0001c0001t0006g0337a0001c0001t0006g0341a0001c0003t0006g0340others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.331+3346C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090418 | ||||||
| chr7:151090503
|
G | C | 1 | a0001c0001t0005g0126 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.331+3431G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090503 | ||||||
| chr7:151090652
|
C | T | 5 | a0001c0001t0002g0322a0001c0001t0002g0323a0001c0004t0001g0013others(2): Show | 5 | HG01081.hp2 HG02970.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.331+3580C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090652 | ||||||
| chr7:151090714
|
C | T | 3 | a0001c0001t0002g0333a0001c0001t0002g0335a0005c0012t0002g0334 | 3 | HG03209.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.331+3642C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090714 | ||||||
| chr7:151090718
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.331+3646C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090718 | ||||||
| chr7:151090743
|
A | G | 306 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(303): Show | 315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.331+3671A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090743 | ||||||
| chr7:151090801
|
G | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(113): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.331+3729G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090801 | ||||||
| chr7:151090804
|
C | T | 6 | a0001c0001t0006g0337a0001c0001t0006g0341a0001c0003t0006g0340others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.331+3732C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090804 | ||||||
| chr7:151090812
|
C | A | 1 | a0001c0001t0002g0325 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.331+3740C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090812 | ||||||
| chr7:151090878
|
A | G | 2 | a0001c0001t0004g0023a0001c0001t0004g0090 | 2 | HG02080.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.331+3806A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090878 | ||||||
| chr7:151091114
|
C | G | 1 | a0001c0001t0001g0098 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.331+4042C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151091114 | ||||||
| chr7:151091173
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.331+4101G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151091173 | ||||||
| chr7:151091217
|
T | C | 313 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(310): Show | 322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.331+4145T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151091217 | ||||||
| chr7:151091335
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0270 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.331+4263C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151091335 | ||||||
| chr7:151091348
|
G | A | 3 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0324 | 3 | HG01109.hp1 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.331+4276G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151091348 | ||||||
| chr7:151091506
|
C | A | 6 | a0001c0001t0006g0337a0001c0001t0006g0341a0001c0003t0006g0340others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.331+4434C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151091506 | ||||||
| chr7:151091590
|
A | G | 100 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(97): Show | 101 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.331+4518A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151091590 | ||||||
| chr7:151091697
|
C | A | 1 | a0001c0001t0001g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.331+4625C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151091697 | ||||||
| chr7:151091812
|
T | C | 3 | a0001c0005t0006g0336a0001c0005t0006g0338a0001c0005t0006g0339 | 3 | HG02257.hp2 HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.331+4740T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151091812 | ||||||
| chr7:151092021
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.331+4949G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092021 | ||||||
| chr7:151092469
|
G | C | 97 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(94): Show | 98 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.331+5397G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092469 | ||||||
| chr7:151092505
|
G | T | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.331+5433G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092505 | ||||||
| chr7:151092516
|
C | T | 97 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(94): Show | 98 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.331+5444C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092516 | ||||||
| chr7:151092564
|
C | T | 4 | a0001c0001t0002g0309a0001c0001t0006g0337a0001c0001t0006g0341others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.331+5492C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092564 | ||||||
| chr7:151092565
|
G | A | 1 | a0001c0003t0001g0027 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.331+5493G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092565 | ||||||
| chr7:151092674
|
C | G | 41 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(38): Show | 44 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.331+5602C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092674 | ||||||
| chr7:151092704
|
C | A | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.331+5632C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092704 | ||||||
| chr7:151092704
|
C | G | 73 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0116others(70): Show | 77 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.331+5632C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092704 | ||||||
| chr7:151092912
|
A | G | 2 | a0001c0001t0002g0300a0001c0001t0002g0324 | 2 | HG01109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.331+5840A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092912 | ||||||
| chr7:151092951
|
G | T | 1 | a0001c0001t0001g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.331+5879G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092951 | ||||||
| chr7:151093001
|
G | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG00735.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.331+5929G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151093001 | ||||||
| chr7:151093032
|
C | T | 97 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(94): Show | 98 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.331+5960C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151093032 | ||||||
| chr7:151093107
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.331+6035T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151093107 | ||||||
| chr7:151093265
|
C | T | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0291 | 3 | NA18975.hp1 NA18980.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.331+6193C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151093265 | ||||||
| chr7:151093563
|
G | T | 1 | a0001c0001t0001g0267 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.331+6491G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151093563 | ||||||
| chr7:151093620
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.331+6548G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151093620 | ||||||
| chr7:151093622
|
C | CTCTTTGC others(5): Show |
1 | a0001c0001t0002g0138 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+6552_331+6563d others(14): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151093622 | |||||
| chr7:151093654
|
G | A | 6 | a0001c0001t0006g0337a0001c0001t0006g0341a0001c0003t0006g0340others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.331+6582G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151093654 | ||||||
| chr7:151093843
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.331+6771G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151093843 | ||||||
| chr7:151093932
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0175 | 2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.331+6860C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151093932 | ||||||
| chr7:151093949
|
A | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(115): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.331+6877A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151093949 | ||||||
| chr7:151094165
|
C | T | 291 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(288): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.331+7093C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151094165 | ||||||
| chr7:151094228
|
T | TGAAA | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(169): Show | 177 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.331+7158_331+7161d others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151094228 | |||||
| chr7:151094346
|
C | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0136a0001c0003t0001g0134others(2): Show | 5 | HG01952.hp2 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+7274C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151094346 | ||||||
| chr7:151094479
|
GA | G | 6 | a0001c0001t0001g0177a0001c0001t0002g0304a0001c0001t0002g0333others(3): Show | 6 | HG01515.hp1 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.331+7421delA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151094479 | |||||
| chr7:151094543
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.331+7471G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151094543 | ||||||
| chr7:151094592
|
T | C | 320 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(317): Show | 329 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.331+7520T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151094592 | ||||||
| chr7:151094873
|
C | CCCTT | 3 | a0001c0001t0002g0333a0001c0001t0002g0335a0005c0012t0002g0334 | 3 | HG03209.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.331+7821_331+7824d others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151094873 | |||||
| chr7:151094942
|
G | A | 1 | a0001c0001t0001g0004 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.331+7870G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151094942 | ||||||
| chr7:151095184
|
G | A | 294 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.331+8112G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151095184 | ||||||
| chr7:151095212
|
T | C | 1 | a0001c0001t0002g0010 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.331+8140T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151095212 | ||||||
| chr7:151095345
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.331+8273G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151095345 | ||||||
| chr7:151095450
|
C | T | 294 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.331+8378C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151095450 | ||||||
| chr7:151095537
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0018t0001g0108 | 3 | HG02280.hp2 HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.331+8465G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151095537 | ||||||
| chr7:151095701
|
CA | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(52): Show | 56 | HG00544.hp1 HG00609.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.331+8655delA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151095701 | |||||
| chr7:151095701
|
CAA | C | 207 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(204): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.331+8654_331+8655d others(4): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151095701 | |||||
| chr7:151095701
|
CAAA | C | 53 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0097others(50): Show | 56 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.331+8653_331+8655d others(5): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151095701 | |||||
| chr7:151095702
|
A | C | 1 | a0001c0001t0001g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.331+8630A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151095702 | ||||||
| chr7:151095962
|
A | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0174others(1): Show | 4 | HG03098.hp1 HG03579.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.331+8890A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151095962 | ||||||
| chr7:151096005
|
G | A | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0003g0281 | 3 | HG02896.hp2 HG02897.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.331+8933G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096005 | ||||||
| chr7:151096254
|
C | T | 4 | a0001c0001t0001g0089a0001c0001t0001g0181a0001c0001t0001g0266others(1): Show | 4 | HG00735.hp1 HG02015.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.331+9182C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096254 | ||||||
| chr7:151096338
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.331+9266G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096338 | ||||||
| chr7:151096369
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.331+9297G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096369 | ||||||
| chr7:151096383
|
TC | T | 98 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(95): Show | 99 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.331+9312delC | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096383 | ||||||
| chr7:151096445
|
C | T | 1 | a0001c0003t0001g0168 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.331+9373C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096445 | ||||||
| chr7:151096504
|
G | A | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(1): Show | 4 | HG02486.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.331+9432G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096504 | ||||||
| chr7:151096523
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.331+9451A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096523 | ||||||
| chr7:151096541
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.331+9469C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096541 | ||||||
| chr7:151096597
|
C | T | 9 | a0001c0001t0002g0010a0001c0001t0002g0158a0001c0001t0002g0159others(6): Show | 9 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.331+9525C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096597 | ||||||
| chr7:151096629
|
C | T | 3 | a0001c0001t0002g0297a0001c0001t0002g0298a0001c0001t0002g0332 | 3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.331+9557C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096629 | ||||||
| chr7:151096633
|
C | T | 1 | a0001c0004t0001g0132 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.331+9561C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096633 | ||||||
| chr7:151096686
|
G | A | 1 | a0001c0001t0002g0330 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.331+9614G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096686 | ||||||
| chr7:151096717
|
C | G | 1 | a0001c0001t0002g0138 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+9645C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096717 | ||||||
| chr7:151096719
|
G | C | 1 | a0001c0001t0002g0138 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+9647G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096719 | ||||||
| chr7:151096811
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.331+9739C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096811 | ||||||
| chr7:151096839
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.331+9767T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096839 | ||||||
| chr7:151096872
|
G | A | 98 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(95): Show | 99 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.331+9800G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096872 | ||||||
| chr7:151096957
|
G | A | 2 | a0001c0001t0001g0197a0001c0001t0009g0204 | 2 | NA18944.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.331+9885G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096957 | ||||||
| chr7:151096982
|
A | T | 1 | a0001c0001t0002g0138 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+9910A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096982 | ||||||
| chr7:151096983
|
C | A | 1 | a0001c0001t0002g0138 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+9911C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096983 | ||||||
| chr7:151097058
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.331+9986G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097058 | ||||||
| chr7:151097294
|
G | C | 1 | a0001c0001t0002g0138 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+10222G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097294 | ||||||
| chr7:151097295
|
C | G | 1 | a0001c0001t0002g0138 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+10223C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097295 | ||||||
| chr7:151097297
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.331+10225G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097297 | ||||||
| chr7:151097391
|
C | G | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.331+10319C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097391 | ||||||
| chr7:151097424
|
C | G | 3 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0002g0295 | 3 | HG01167.hp1 HG01169.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.331+10352C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097424 | ||||||
| chr7:151097424
|
C | T | 1 | a0001c0001t0002g0296 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.331+10352C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097424 | ||||||
| chr7:151097517
|
C | CA | 7 | a0001c0001t0001g0282a0001c0001t0002g0297a0001c0001t0002g0298others(4): Show | 7 | HG01081.hp2 HG01109.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.331+10463dupA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151097517 | |||||
| chr7:151097517
|
CA | C | 160 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(157): Show | 165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.331+10463delA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151097517 | |||||
| chr7:151097614
|
G | T | 1 | a0001c0001t0002g0138 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+10542G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097614 | ||||||
| chr7:151097639
|
G | C | 310 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(307): Show | 319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.331+10567G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097639 | ||||||
| chr7:151097773
|
C | A | 1 | a0001c0001t0001g0024 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.331+10701C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097773 | ||||||
| chr7:151097887
|
T | C | 1 | a0001c0001t0002g0304 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.331+10815T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097887 | ||||||
| chr7:151097967
|
G | T | 1 | a0001c0001t0002g0138 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+10895G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097967 | ||||||
| chr7:151098002
|
C | G | 1 | a0001c0001t0002g0010 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.331+10930C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098002 | ||||||
| chr7:151098044
|
G | C | 1 | a0001c0001t0002g0138 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+10972G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098044 | ||||||
| chr7:151098045
|
C | G | 1 | a0001c0001t0002g0138 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+10973C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098045 | ||||||
| chr7:151098084
|
C | T | 1 | a0001c0001t0003g0104 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.331+11012C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098084 | ||||||
| chr7:151098455
|
A | C | 1 | a0001c0001t0002g0138 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+11383A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098455 | ||||||
| chr7:151098456
|
C | A | 1 | a0001c0001t0002g0138 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+11384C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098456 | ||||||
| chr7:151098498
|
A | T | 1 | a0001c0001t0002g0330 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.331+11426A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098498 | ||||||
| chr7:151098522
|
G | A | 293 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(290): Show | 302 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.331+11450G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098522 | ||||||
| chr7:151098529
|
T | G | 115 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(112): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.331+11457T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098529 | ||||||
| chr7:151098630
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.331+11558G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098630 | ||||||
| chr7:151098733
|
C | CT | 75 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0026others(72): Show | 79 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.331+11680dupT | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151098733 | |||||
| chr7:151098733
|
CT | C | 125 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(122): Show | 129 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.331+11680delT | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151098733 | |||||
| chr7:151098733
|
CTT | C | 7 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0195others(4): Show | 7 | HG00323.hp1 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.331+11679_331+1168 others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151098733 | |||||
| chr7:151098738
|
T | C | 2 | a0001c0001t0002g0301a0001c0001t0002g0305 | 2 | HG02735.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.331+11666T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098738 | ||||||
| chr7:151098854
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0290 | 3 | HG03017.hp1 HG03688.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.331+11782C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098854 | ||||||
| chr7:151098894
|
C | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0136a0001c0003t0001g0134others(2): Show | 5 | HG01952.hp2 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+11822C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098894 | ||||||
| chr7:151098982
|
C | T | 293 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(290): Show | 302 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.331+11910C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098982 | ||||||
| chr7:151098983
|
A | G | 319 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(316): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.331+11911A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098983 | ||||||
| chr7:151099021
|
C | A | 1 | a0001c0001t0002g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.331+11949C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099021 | ||||||
| chr7:151099113
|
G | C | 179 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(176): Show | 184 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.331+12041G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099113 | ||||||
| chr7:151099160
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.331+12088A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099160 | ||||||
| chr7:151099334
|
C | A | 14 | a0001c0001t0002g0178a0001c0001t0002g0313a0001c0002t0002g0310others(11): Show | 14 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.331+12262C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099334 | ||||||
| chr7:151099339
|
T | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(95): Show | 99 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.331+12267T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099339 | ||||||
| chr7:151099342
|
C | CA | 95 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(92): Show | 96 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.331+12287dupA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151099342 | |||||
| chr7:151099342
|
CA | C | 189 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(186): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.331+12287delA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151099342 | |||||
| chr7:151099365
|
A | C | 3 | a0001c0001t0002g0333a0001c0001t0002g0335a0005c0012t0002g0334 | 3 | HG03209.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.331+12293A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099365 | ||||||
| chr7:151099432
|
TG | T | 290 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(287): Show | 299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.331+12361delG | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099432 | ||||||
| chr7:151099581
|
T | G | 1 | a0001c0001t0003g0209 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.331+12509T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099581 | ||||||
| chr7:151099674
|
C | T | 13 | a0001c0001t0002g0178a0001c0001t0002g0313a0001c0002t0002g0310others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.331+12602C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099674 | ||||||
| chr7:151099692
|
A | T | 3 | a0001c0005t0006g0336a0001c0005t0006g0338a0001c0005t0006g0339 | 3 | HG02257.hp2 HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.331+12620A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099692 | ||||||
| chr7:151099724
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.331+12652G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099724 | ||||||
| chr7:151099819
|
T | C | 77 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(74): Show | 81 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.331+12747T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099819 | ||||||
| chr7:151099840
|
T | A | 77 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(74): Show | 81 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.331+12768T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099840 | ||||||
| chr7:151099859
|
T | C | 290 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(287): Show | 299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.331+12787T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099859 | ||||||
| chr7:151099967
|
C | A | 3 | a0001c0001t0006g0337a0001c0001t0006g0341a0001c0003t0006g0340 | 3 | HG01891.hp2 HG02451.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.331+12895C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099967 | ||||||
| chr7:151100002
|
T | C | 290 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(287): Show | 299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.331+12930T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100002 | ||||||
| chr7:151100052
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.331+12980C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100052 | ||||||
| chr7:151100147
|
G | A | 30 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0109others(27): Show | 33 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.331+13075G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100147 | ||||||
| chr7:151100165
|
T | C | 319 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(316): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.331+13093T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100165 | ||||||
| chr7:151100209
|
C | A | 1 | a0001c0001t0001g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.331+13137C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100209 | ||||||
| chr7:151100319
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.331+13247C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100319 | ||||||
| chr7:151100332
|
G | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0181a0001c0001t0001g0197others(5): Show | 9 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.331+13260G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100332 | ||||||
| chr7:151100478
|
T | C | 1 | a0001c0001t0002g0140 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.331+13406T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100478 | ||||||
| chr7:151100494
|
G | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(112): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.331+13422G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100494 | ||||||
| chr7:151100494
|
G | T | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(1): Show | 4 | HG02486.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.331+13422G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100494 | ||||||
| chr7:151100611
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.331+13539C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100611 | ||||||
| chr7:151100899
|
C | T | 3 | a0001c0001t0002g0297a0001c0001t0002g0298a0001c0001t0002g0332 | 3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.331+13827C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100899 | ||||||
| chr7:151101040
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.331+13968C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151101040 | ||||||
| chr7:151101063
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.331+13991G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151101063 | ||||||
| chr7:151101564
|
C | T | 319 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(316): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.331+14492C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151101564 | ||||||
| chr7:151101639
|
T | C | 296 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.331+14567T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151101639 | ||||||
| chr7:151101893
|
G | A | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(169): Show | 177 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.331+14821G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151101893 | ||||||
| chr7:151101962
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.332-14831G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151101962 | ||||||
| chr7:151101986
|
G | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(115): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.332-14807G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151101986 | ||||||
| chr7:151102072
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.332-14721C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102072 | ||||||
| chr7:151102104
|
C | T | 3 | a0001c0001t0006g0337a0001c0001t0006g0341a0001c0003t0006g0340 | 3 | HG01891.hp2 HG02451.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.332-14689C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102104 | ||||||
| chr7:151102212
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.332-14581C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102212 | ||||||
| chr7:151102230
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0175 | 2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.332-14563C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102230 | ||||||
| chr7:151102291
|
G | A | 1 | a0001c0001t0002g0304 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.332-14502G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102291 | ||||||
| chr7:151102292
|
T | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(112): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.332-14501T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102292 | ||||||
| chr7:151102345
|
C | T | 3 | a0001c0001t0002g0333a0001c0001t0002g0335a0005c0012t0002g0334 | 3 | HG03209.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.332-14448C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102345 | ||||||
| chr7:151102385
|
A | G | 1 | a0001c0001t0002g0304 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.332-14408A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102385 | ||||||
| chr7:151102598
|
C | CA | 120 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.332-14178dupA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151102598 | |||||
| chr7:151102598
|
C | CAA | 8 | a0001c0001t0001g0212a0001c0001t0001g0267a0001c0001t0001g0268others(5): Show | 8 | HG01192.hp1 HG02056.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.332-14179_332-1417 others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151102598 | |||||
| chr7:151102598
|
CA | C | 71 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(68): Show | 75 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.332-14178delA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151102598 | |||||
| chr7:151102609
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.332-14184A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102609 | ||||||
| chr7:151102616
|
T | A | 2 | a0001c0001t0001g0185a0001c0001t0001g0211 | 2 | NA18969.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.332-14177T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102616 | ||||||
| chr7:151102663
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.332-14130C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102663 | ||||||
| chr7:151102774
|
C | G | 1 | a0001c0001t0002g0330 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.332-14019C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102774 | ||||||
| chr7:151102781
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.332-14012A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102781 | ||||||
| chr7:151102831
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.332-13962G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102831 | ||||||
| chr7:151102887
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0082 | 2 | HG01257.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.332-13906C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102887 | ||||||
| chr7:151102969
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0080a0001c0001t0001g0081 | 3 | HG02717.hp1 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.332-13824C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102969 | ||||||
| chr7:151103148
|
C | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0120 | 2 | HG00639.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.332-13645C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103148 | ||||||
| chr7:151103154
|
T | G | 1 | a0001c0001t0005g0141 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.332-13639T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103154 | ||||||
| chr7:151103173
|
T | G | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.332-13620T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103173 | ||||||
| chr7:151103317
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.332-13476A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103317 | ||||||
| chr7:151103398
|
G | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(112): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.332-13395G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103398 | ||||||
| chr7:151103422
|
A | C | 1 | a0001c0001t0005g0141 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.332-13371A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103422 | ||||||
| chr7:151103449
|
A | C | 1 | a0001c0001t0005g0141 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.332-13344A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103449 | ||||||
| chr7:151103450
|
C | A | 1 | a0001c0001t0005g0141 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.332-13343C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103450 | ||||||
| chr7:151103491
|
G | A | 1 | a0001c0018t0001g0108 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.332-13302G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103491 | ||||||
| chr7:151103514
|
G | A | 5 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0214others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-13279G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103514 | ||||||
| chr7:151103534
|
A | G | 2 | a0001c0001t0001g0125a0001c0001t0001g0175 | 2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.332-13259A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103534 | ||||||
| chr7:151103652
|
A | G | 292 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(289): Show | 301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.332-13141A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103652 | ||||||
| chr7:151103736
|
G | T | 290 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(287): Show | 299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.332-13057G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103736 | ||||||
| chr7:151103867
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.332-12926C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103867 | ||||||
| chr7:151104001
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.332-12792G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104001 | ||||||
| chr7:151104002
|
T | TG | 5 | a0001c0001t0001g0041a0001c0001t0001g0079a0001c0001t0002g0109others(2): Show | 5 | HG00642.hp1 HG02056.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-12789dupG | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151104002 | |||||
| chr7:151104005
|
C | G | 319 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(316): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.332-12788C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104005 | ||||||
| chr7:151104009
|
G | A | 2 | a0001c0001t0001g0107a0001c0018t0001g0108 | 2 | HG02280.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.332-12784G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104009 | ||||||
| chr7:151104079
|
G | T | 1 | a0001c0001t0002g0330 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.332-12714G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104079 | ||||||
| chr7:151104151
|
A | G | 74 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(71): Show | 78 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.332-12642A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104151 | ||||||
| chr7:151104242
|
G | C | 3 | a0001c0001t0002g0297a0001c0001t0002g0298a0001c0001t0002g0332 | 3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.332-12551G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104242 | ||||||
| chr7:151104253
|
T | C | 300 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(297): Show | 309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.332-12540T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104253 | ||||||
| chr7:151104256
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0018t0001g0108 | 3 | HG02280.hp2 HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.332-12537C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104256 | ||||||
| chr7:151104333
|
C | A | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.332-12460C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104333 | ||||||
| chr7:151104406
|
G | A | 1 | a0001c0001t0002g0302 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.332-12387G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104406 | ||||||
| chr7:151104430
|
G | T | 1 | a0001c0001t0001g0261 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.332-12363G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104430 | ||||||
| chr7:151104478
|
A | G | 1 | a0001c0001t0001g0280 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.332-12315A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104478 | ||||||
| chr7:151104562
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0050a0001c0001t0001g0051 | 3 | NA18951.hp1 NA18986.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.332-12231G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104562 | ||||||
| chr7:151104563
|
C | A | 2 | a0001c0001t0001g0107a0001c0018t0001g0108 | 2 | HG02280.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.332-12230C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104563 | ||||||
| chr7:151104584
|
G | C | 14 | a0001c0001t0002g0178a0001c0001t0002g0313a0001c0002t0002g0310others(11): Show | 14 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.332-12209G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104584 | ||||||
| chr7:151104585
|
C | T | 11 | a0001c0001t0001g0026a0001c0001t0001g0123a0001c0001t0001g0130others(8): Show | 11 | HG01952.hp2 HG02027.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.332-12208C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104585 | ||||||
| chr7:151104720
|
A | T | 1 | a0001c0001t0001g0047 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.332-12073A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104720 | ||||||
| chr7:151104764
|
G | A | 1 | a0001c0001t0005g0141 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.332-12029G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104764 | ||||||
| chr7:151104765
|
A | G | 1 | a0001c0001t0005g0141 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.332-12028A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104765 | ||||||
| chr7:151104862
|
AAGAACGG others(2): Show |
A | 3 | a0001c0004t0001g0013a0001c0004t0001g0014a0001c0004t0001g0016 | 3 | HG02970.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.332-11925_332-1191 others(13): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151104862 | |||||
| chr7:151104970
|
C | T | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.332-11823C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104970 | ||||||
| chr7:151104981
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.332-11812G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104981 | ||||||
| chr7:151104982
|
A | G | 1 | a0001c0001t0001g0047 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.332-11811A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104982 | ||||||
| chr7:151105314
|
T | A | 1 | a0001c0001t0002g0304 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.332-11479T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105314 | ||||||
| chr7:151105365
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0174 | 3 | HG03098.hp1 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.332-11428C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105365 | ||||||
| chr7:151105421
|
A | G | 3 | a0001c0001t0001g0083a0001c0001t0001g0120a0006c0015t0001g0124 | 3 | HG00140.hp1 HG00639.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.332-11372A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105421 | ||||||
| chr7:151105592
|
C | CA | 6 | a0001c0001t0001g0079a0001c0001t0001g0098a0001c0001t0001g0267others(3): Show | 6 | HG00642.hp1 HG02738.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.332-11187dupA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105592 | |||||
| chr7:151105606
|
A | G | 1 | a0001c0001t0005g0141 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.332-11187A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105606 | ||||||
| chr7:151105607
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0005g0141 | 2 | NA18961.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.332-11186G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105607 | ||||||
| chr7:151105736
|
C | T | 23 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0109others(20): Show | 26 | HG00408.hp1 HG00597.hp1 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.332-11057C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105736 | ||||||
| chr7:151105776
|
G | GC | 64 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0072others(61): Show | 68 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.332-11006dupC | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105776 | |||||
| chr7:151105776
|
G | GCC | 16 | a0001c0001t0001g0039a0001c0001t0001g0078a0001c0001t0001g0121others(13): Show | 16 | HG00408.hp1 HG00558.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.332-11007_332-1100 others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105776 | |||||
| chr7:151105776
|
G | GCCCCC | 15 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0029others(12): Show | 15 | HG00741.hp2 HG01952.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.332-11010_332-1100 others(9): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105776 | |||||
| chr7:151105776
|
G | GCCCCCC | 24 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0032others(21): Show | 24 | HG00673.hp2 HG00733.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.332-11011_332-1100 others(10): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105776 | |||||
| chr7:151105776
|
G | GCCCCCCC | 22 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0036others(19): Show | 23 | HG00544.hp1 HG00609.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.332-11012_332-1100 others(11): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105776 | |||||
| chr7:151105776
|
G | GCCCCCCC others(1): Show |
15 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0030others(12): Show | 15 | HG00099.hp2 HG00438.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.332-11013_332-1100 others(12): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105776 | |||||
| chr7:151105776
|
G | GCCCCCCC others(3): Show |
1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.332-11015_332-1100 others(14): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105776 | |||||
| chr7:151105776
|
G | GCCCCCCC others(4): Show |
1 | a0001c0001t0001g0085 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.332-11016_332-1100 others(15): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105776 | |||||
| chr7:151105787
|
CGA | C | 4 | a0001c0001t0007g0152a0001c0002t0002g0317a0001c0002t0002g0318others(1): Show | 4 | HG02280.hp1 HG03540.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-11005_332-1100 others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105787 | ||||||
| chr7:151105788
|
G | C | 13 | a0001c0001t0001g0028a0001c0001t0001g0053a0001c0001t0001g0097others(10): Show | 13 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.332-11005G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105788 | ||||||
| chr7:151105789
|
A | C | 15 | a0001c0001t0001g0028a0001c0001t0001g0053a0001c0001t0001g0077others(12): Show | 15 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.332-11004A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105789 | ||||||
| chr7:151105791
|
A | C | 17 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0053others(14): Show | 17 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.332-11002A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105791 | ||||||
| chr7:151105791
|
A | G | 3 | a0001c0001t0002g0150a0001c0001t0005g0169a0001c0001t0007g0152 | 3 | HG02523.hp2 NA18986.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.332-11002A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105791 | ||||||
| chr7:151105792
|
C | A | 3 | a0001c0001t0002g0150a0001c0001t0005g0169a0001c0001t0007g0152 | 3 | HG02523.hp2 NA18986.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.332-11001C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105792 | ||||||
| chr7:151105792
|
C | CCA | 23 | a0001c0001t0001g0036a0001c0001t0001g0056a0001c0001t0001g0071others(20): Show | 23 | HG00642.hp2 HG00735.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.332-10962_332-1096 others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | |||||
| chr7:151105792
|
C | CCACA | 96 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(93): Show | 97 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.332-10964_332-1096 others(8): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | |||||
| chr7:151105792
|
C | CCACAACA others(8): Show |
1 | a0001c0001t0001g0267 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.332-10997_332-1099 others(19): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | |||||
| chr7:151105792
|
C | CCACACA | 41 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(38): Show | 44 | HG00140.hp2 HG00673.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.332-10966_332-1096 others(10): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | |||||
| chr7:151105792
|
C | CCACACAC others(1): Show |
30 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0030others(27): Show | 31 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.332-10968_332-1096 others(12): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | |||||
| chr7:151105792
|
C | CCACACAC others(3): Show |
20 | a0001c0001t0001g0045a0001c0001t0001g0057a0001c0001t0001g0073others(17): Show | 20 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.332-10970_332-1096 others(14): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | |||||
| chr7:151105792
|
C | CCACACAC others(5): Show |
12 | a0001c0001t0001g0078a0001c0001t0001g0183a0001c0001t0001g0188others(9): Show | 12 | HG00423.hp1 HG02056.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.332-10972_332-1096 others(16): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | |||||
| chr7:151105792
|
C | CCACACAC others(7): Show |
4 | a0001c0001t0001g0187a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | NA18970.hp2 NA19056.hp1 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-10974_332-1096 others(18): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | |||||
| chr7:151105792
|
C | CCACACAC others(9): Show |
3 | a0001c0001t0001g0004a0001c0001t0001g0107a0001c0005t0006g0338 | 4 | HG01257.hp1 HG01258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-10976_332-1096 others(20): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | |||||
| chr7:151105792
|
C | CCACACAC others(11): Show |
1 | a0001c0001t0001g0118 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.332-10978_332-1096 others(22): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | |||||
| chr7:151105792
|
C | CCACACAC others(13): Show |
5 | a0001c0001t0001g0119a0001c0001t0001g0181a0001c0001t0001g0216others(2): Show | 5 | HG02015.hp1 HG02129.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-10980_332-1096 others(24): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | |||||
| chr7:151105792
|
C | CCACACAC others(15): Show |
4 | a0001c0001t0001g0083a0001c0001t0001g0116a0001c0001t0001g0117others(1): Show | 4 | HG00140.hp1 HG02486.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.332-10982_332-1096 others(26): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | |||||
| chr7:151105792
|
C | CCACACAC others(17): Show |
2 | a0001c0001t0001g0120a0001c0004t0001g0132 | 2 | HG00639.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.332-10984_332-1096 others(28): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | |||||
| chr7:151105792
|
C | CCACACAC others(19): Show |
1 | a0001c0001t0001g0122 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.332-10986_332-1096 others(30): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | |||||
| chr7:151105792
|
C | CCACACAC others(21): Show |
1 | a0001c0001t0001g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.332-10988_332-1096 others(32): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | |||||
| chr7:151105792
|
C | CCACACAC others(23): Show |
4 | a0001c0001t0001g0121a0001c0001t0001g0125a0001c0001t0001g0129others(1): Show | 4 | HG02109.hp2 HG02257.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-10990_332-1096 others(34): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | |||||
| chr7:151105792
|
CCA | C | 15 | a0001c0001t0001g0182a0001c0001t0001g0192a0001c0001t0001g0210others(12): Show | 15 | HG00408.hp1 HG00544.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.332-10962_332-1096 others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | |||||
| chr7:151105792
|
CCACA | C | 25 | a0001c0001t0001g0072a0001c0001t0001g0127a0001c0001t0001g0175others(22): Show | 28 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.332-10964_332-1096 others(8): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | |||||
| chr7:151105793
|
C | G | 10 | a0001c0002t0002g0310a0001c0002t0002g0311a0001c0002t0002g0312others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.332-11000C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105793 | ||||||
| chr7:151105794
|
A | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0077 | 2 | HG04115.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.332-10999A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105794 | ||||||
| chr7:151105796
|
A | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0077 | 2 | HG04115.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.332-10997A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105796 | ||||||
| chr7:151105797
|
C | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0077 | 2 | HG04115.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.332-10996C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105797 | ||||||
| chr7:151105797
|
CA | C | 12 | a0001c0001t0001g0028a0001c0001t0002g0178a0001c0002t0002g0310others(9): Show | 12 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.332-10995delA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105797 | ||||||
| chr7:151105869
|
C | CT | 152 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0017others(149): Show | 156 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.332-10910dupT | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105869 | |||||
| chr7:151105869
|
C | CTT | 110 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 114 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.332-10911_332-1091 others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105869 | |||||
| chr7:151105869
|
CT | C | 6 | a0001c0001t0001g0020a0001c0001t0002g0304a0001c0003t0006g0340others(3): Show | 6 | HG01515.hp1 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.332-10910delT | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105869 | |||||
| chr7:151105884
|
A | T | 6 | a0001c0001t0001g0182a0001c0001t0001g0192a0001c0001t0001g0268others(3): Show | 6 | NA18975.hp1 NA18980.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.332-10909A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105884 | ||||||
| chr7:151106009
|
A | T | 1 | a0001c0001t0001g0263 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.332-10784A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151106009 | ||||||
| chr7:151106138
|
T | G | 2 | a0001c0001t0001g0185a0001c0001t0001g0211 | 2 | NA18969.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.332-10655T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151106138 | ||||||
| chr7:151106275
|
TCTTTC | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0078others(12): Show | 16 | HG00140.hp1 HG00639.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.332-10513_332-1050 others(9): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151106275 | |||||
| chr7:151106462
|
A | G | 287 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(284): Show | 295 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.332-10331A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151106462 | ||||||
| chr7:151106678
|
C | T | 319 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(316): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.332-10115C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151106678 | ||||||
| chr7:151106719
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0216 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.332-10074C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151106719 | ||||||
| chr7:151106720
|
G | A | 2 | a0001c0007t0002g0316a0001c0007t0002g0320 | 2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.332-10073G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151106720 | ||||||
| chr7:151106784
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.332-10009C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151106784 | ||||||
| chr7:151106785
|
G | A | 2 | a0001c0004t0001g0013a0001c0004t0001g0014 | 2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.332-10008G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151106785 | ||||||
| chr7:151106813
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.332-9980C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151106813 | ||||||
| chr7:151107183
|
A | G | 33 | a0001c0001t0001g0127a0001c0001t0002g0001a0001c0001t0002g0005others(30): Show | 36 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.332-9610A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107183 | ||||||
| chr7:151107235
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.332-9558G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107235 | ||||||
| chr7:151107310
|
C | CA | 23 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0058others(20): Show | 24 | HG00140.hp1 HG00639.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.332-9466dupA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151107310 | |||||
| chr7:151107317
|
A | AG | 48 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0107others(45): Show | 51 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.332-9476_332-9475i others(3): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107317 | ||||||
| chr7:151107317
|
A | G | 1 | a0001c0001t0002g0155 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.332-9476A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107317 | ||||||
| chr7:151107352
|
G | C | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.332-9441G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107352 | ||||||
| chr7:151107486
|
C | T | 7 | a0001c0001t0002g0159a0001c0001t0002g0160a0001c0001t0002g0161others(4): Show | 7 | HG02622.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.332-9307C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107486 | ||||||
| chr7:151107512
|
T | C | 3 | a0001c0005t0006g0336a0001c0005t0006g0338a0001c0005t0006g0339 | 3 | HG02257.hp2 HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.332-9281T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107512 | ||||||
| chr7:151107580
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.332-9213C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107580 | ||||||
| chr7:151107581
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.332-9212G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107581 | ||||||
| chr7:151107628
|
A | T | 52 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(49): Show | 56 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.332-9165A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107628 | ||||||
| chr7:151107686
|
T | C | 1 | a0001c0001t0009g0204 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.332-9107T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107686 | ||||||
| chr7:151107811
|
C | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0122 | 3 | HG01257.hp1 HG01258.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.332-8982C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107811 | ||||||
| chr7:151107995
|
C | T | 33 | a0001c0001t0001g0127a0001c0001t0002g0001a0001c0001t0002g0005others(30): Show | 36 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.332-8798C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107995 | ||||||
| chr7:151108050
|
A | G | 48 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0107others(45): Show | 51 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.332-8743A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151108050 | ||||||
| chr7:151108111
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0003g0281a0001c0018t0001g0108 | 3 | HG02280.hp2 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.332-8682C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151108111 | ||||||
| chr7:151108172
|
T | C | 1 | a0001c0001t0002g0309 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.332-8621T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151108172 | ||||||
| chr7:151108185
|
A | G | 284 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(281): Show | 292 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.332-8608A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151108185 | ||||||
| chr7:151108315
|
C | T | 7 | a0001c0001t0002g0159a0001c0001t0002g0160a0001c0001t0002g0161others(4): Show | 7 | HG02622.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.332-8478C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151108315 | ||||||
| chr7:151108392
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.332-8401C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151108392 | ||||||
| chr7:151108424
|
C | G | 1 | a0001c0001t0001g0074 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.332-8369C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151108424 | ||||||
| chr7:151108455
|
C | G | 1 | a0001c0001t0001g0263 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.332-8338C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151108455 | ||||||
| chr7:151108545
|
T | A | 3 | a0001c0001t0002g0297a0001c0001t0002g0298a0001c0001t0002g0332 | 3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.332-8248T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151108545 | ||||||
| chr7:151109037
|
T | C | 15 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0078others(12): Show | 16 | HG00140.hp1 HG00639.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.332-7756T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109037 | ||||||
| chr7:151109055
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.332-7738C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109055 | ||||||
| chr7:151109069
|
T | C | 1 | a0001c0001t0003g0104 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.332-7724T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109069 | ||||||
| chr7:151109165
|
T | TA | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(206): Show | 213 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.332-7613dupA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151109165 | |||||
| chr7:151109165
|
T | TAA | 21 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0029others(18): Show | 22 | HG00544.hp1 HG00741.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.332-7614_332-7613d others(4): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151109165 | |||||
| chr7:151109168
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0002g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.332-7618_332-7606d others(15): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151109168 | |||||
| chr7:151109174
|
A | AC | 38 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0127others(35): Show | 41 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-7619_332-7618i others(3): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109174 | ||||||
| chr7:151109174
|
A | C | 6 | a0001c0001t0002g0333a0001c0001t0002g0335a0001c0004t0001g0013others(3): Show | 6 | HG02970.hp1 HG03209.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.332-7619A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109174 | ||||||
| chr7:151109181
|
C | A | 5 | a0001c0001t0001g0063a0001c0001t0002g0128a0001c0001t0004g0023others(2): Show | 5 | HG01167.hp2 HG02080.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-7612C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109181 | ||||||
| chr7:151109235
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.332-7558T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109235 | ||||||
| chr7:151109239
|
T | TA | 68 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(65): Show | 71 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.332-7551dupA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151109239 | |||||
| chr7:151109240
|
A | C | 3 | a0001c0004t0001g0013a0001c0004t0001g0014a0001c0004t0001g0016 | 3 | HG02970.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.332-7553A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109240 | ||||||
| chr7:151109263
|
C | T | 11 | a0001c0001t0002g0178a0001c0001t0002g0313a0001c0002t0002g0310others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.332-7530C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109263 | ||||||
| chr7:151109289
|
G | C | 3 | a0001c0001t0001g0107a0001c0001t0003g0281a0001c0018t0001g0108 | 3 | HG02280.hp2 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.332-7504G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109289 | ||||||
| chr7:151109533
|
G | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0216 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.332-7260G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109533 | ||||||
| chr7:151109916
|
C | T | 68 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(65): Show | 71 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.332-6877C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109916 | ||||||
| chr7:151109939
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.332-6854G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109939 | ||||||
| chr7:151110151
|
C | T | 1 | a0001c0001t0002g0296 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.332-6642C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110151 | ||||||
| chr7:151110394
|
C | A | 3 | a0001c0004t0001g0013a0001c0004t0001g0014a0001c0004t0001g0016 | 3 | HG02970.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.332-6399C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110394 | ||||||
| chr7:151110417
|
G | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG02258.hp2 HG02717.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-6376G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110417 | ||||||
| chr7:151110558
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.332-6235G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110558 | ||||||
| chr7:151110608
|
C | G | 37 | a0001c0001t0001g0127a0001c0001t0001g0175a0001c0001t0002g0001others(34): Show | 40 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-6185C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110608 | ||||||
| chr7:151110688
|
G | C | 2 | a0001c0002t0002g0310a0001c0002t0002g0311 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.332-6105G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110688 | ||||||
| chr7:151110789
|
C | T | 1 | a0001c0017t0001g0222 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.332-6004C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110789 | ||||||
| chr7:151110856
|
G | A | 38 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0181others(35): Show | 39 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.332-5937G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110856 | ||||||
| chr7:151110885
|
A | G | 307 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(304): Show | 316 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.332-5908A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110885 | ||||||
| chr7:151110889
|
G | C | 4 | a0001c0001t0001g0123a0001c0001t0001g0130a0001c0001t0001g0131others(1): Show | 4 | HG02027.hp1 NA18747.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.332-5904G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110889 | ||||||
| chr7:151110992
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.332-5801C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110992 | ||||||
| chr7:151111021
|
C | T | 3 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0324 | 3 | HG01109.hp1 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.332-5772C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111021 | ||||||
| chr7:151111022
|
G | A | 160 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(157): Show | 162 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.332-5771G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111022 | ||||||
| chr7:151111087
|
C | T | 1 | a0001c0001t0002g0305 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.332-5706C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111087 | ||||||
| chr7:151111124
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.332-5669G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111124 | ||||||
| chr7:151111191
|
A | G | 320 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(317): Show | 329 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.332-5602A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111191 | ||||||
| chr7:151111208
|
C | T | 1 | a0001c0001t0004g0253 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.332-5585C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111208 | ||||||
| chr7:151111374
|
C | T | 3 | a0001c0004t0001g0013a0001c0004t0001g0014a0001c0004t0001g0016 | 3 | HG02970.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.332-5419C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111374 | ||||||
| chr7:151111485
|
T | C | 1 | a0001c0001t0001g0097 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.332-5308T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111485 | ||||||
| chr7:151111488
|
C | A | 1 | a0001c0001t0001g0097 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.332-5305C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111488 | ||||||
| chr7:151111564
|
G | A | 10 | a0001c0001t0001g0175a0001c0001t0006g0337a0001c0001t0006g0341others(7): Show | 10 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.332-5229G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111564 | ||||||
| chr7:151111601
|
C | T | 3 | a0001c0001t0001g0228a0001c0001t0001g0241a0001c0001t0002g0128 | 3 | HG00741.hp1 HG01106.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.332-5192C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111601 | ||||||
| chr7:151111649
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.332-5144C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111649 | ||||||
| chr7:151111662
|
C | T | 338 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(335): Show | 347 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.332-5131C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111662 | ||||||
| chr7:151111791
|
C | G | 1 | a0001c0001t0001g0085 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.332-5002C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111791 | ||||||
| chr7:151112077
|
C | A | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(224): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.332-4716C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112077 | ||||||
| chr7:151112130
|
T | C | 1 | a0001c0001t0002g0330 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.332-4663T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112130 | ||||||
| chr7:151112193
|
C | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(70): Show | 76 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.332-4600C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112193 | ||||||
| chr7:151112245
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0122 | 3 | HG01257.hp1 HG01258.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.332-4548G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112245 | ||||||
| chr7:151112292
|
A | G | 1 | a0001c0001t0005g0142 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.332-4501A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112292 | ||||||
| chr7:151112396
|
C | CGT | 46 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0032others(43): Show | 47 | HG00323.hp1 HG00438.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.332-4358_332-4357d others(4): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | |||||
| chr7:151112396
|
C | CGTGT | 57 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0017others(54): Show | 58 | HG00099.hp2 HG00558.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.332-4360_332-4357d others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | |||||
| chr7:151112396
|
C | CGTGTGT | 12 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0046others(9): Show | 12 | HG00323.hp2 HG01071.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.332-4362_332-4357d others(8): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | |||||
| chr7:151112396
|
C | CGTGTGTG others(1): Show |
8 | a0001c0001t0001g0053a0001c0001t0001g0077a0001c0001t0001g0091others(5): Show | 8 | HG01123.hp1 HG01243.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.332-4364_332-4357d others(10): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | |||||
| chr7:151112396
|
C | CGTGTGTG others(3): Show |
2 | a0001c0001t0001g0079a0001c0001t0003g0252 | 2 | HG00642.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.332-4366_332-4357d others(12): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | |||||
| chr7:151112396
|
C | CGTGTGTG others(9): Show |
1 | a0001c0001t0001g0063 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.332-4372_332-4357d others(18): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | |||||
| chr7:151112396
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.332-4397C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112396 | ||||||
| chr7:151112396
|
CGT | C | 31 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0084others(28): Show | 32 | HG00280.hp2 HG00597.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.332-4358_332-4357d others(4): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | |||||
| chr7:151112396
|
CGTGT | C | 8 | a0001c0001t0001g0110a0001c0001t0001g0211a0001c0001t0001g0229others(5): Show | 8 | HG00099.hp1 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.332-4360_332-4357d others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | |||||
| chr7:151112396
|
CGTGTGT | C | 8 | a0001c0001t0001g0081a0001c0001t0002g0159a0001c0001t0002g0160others(5): Show | 8 | HG02622.hp1 HG02630.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.332-4362_332-4357d others(8): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | |||||
| chr7:151112396
|
CGTGTGTG others(3): Show |
C | 42 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(39): Show | 45 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.332-4366_332-4357d others(12): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | |||||
| chr7:151112396
|
CGTGTGTG others(5): Show |
C | 32 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0020others(29): Show | 33 | HG00140.hp1 HG00639.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.332-4368_332-4357d others(14): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | |||||
| chr7:151112396
|
CGTGTGTG others(21): Show |
C | 2 | a0001c0001t0004g0023a0001c0001t0004g0090 | 2 | HG02080.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.332-4384_332-4357d others(30): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | |||||
| chr7:151112672
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.332-4121C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112672 | ||||||
| chr7:151112675
|
G | A | 1 | a0001c0001t0003g0252 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.332-4118G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112675 | ||||||
| chr7:151112794
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.332-3999G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112794 | ||||||
| chr7:151112883
|
C | T | 1 | a0001c0001t0002g0155 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.332-3910C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112883 | ||||||
| chr7:151112986
|
A | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(72): Show | 78 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.332-3807A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112986 | ||||||
| chr7:151112997
|
G | A | 4 | a0001c0001t0001g0107a0001c0001t0006g0337a0001c0001t0006g0341others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-3796G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112997 | ||||||
| chr7:151113076
|
T | C | 38 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(35): Show | 41 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-3717T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151113076 | ||||||
| chr7:151113139
|
C | G | 1 | a0001c0001t0001g0283 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.332-3654C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151113139 | ||||||
| chr7:151113167
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.332-3626G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151113167 | ||||||
| chr7:151113207
|
T | C | 2 | a0001c0001t0002g0335a0005c0012t0002g0334 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.332-3586T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151113207 | ||||||
| chr7:151113278
|
T | C | 1 | a0001c0005t0006g0338 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.332-3515T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151113278 | ||||||
| chr7:151113366
|
GGGCCTCT others(3): Show |
G | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.332-3421_332-3412d others(12): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151113366 | |||||
| chr7:151113368
|
G | A | 2 | a0001c0001t0003g0281a0001c0018t0001g0108 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.332-3425G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151113368 | ||||||
| chr7:151113574
|
T | G | 4 | a0001c0001t0001g0107a0001c0001t0006g0337a0001c0001t0006g0341others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-3219T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151113574 | ||||||
| chr7:151113676
|
T | C | 148 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(145): Show | 150 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.332-3117T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151113676 | ||||||
| chr7:151113768
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0002g0010 | 2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.332-3025C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151113768 | ||||||
| chr7:151114030
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.332-2763G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151114030 | ||||||
| chr7:151114094
|
G | A | 1 | a0001c0001t0001g0215 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.332-2699G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151114094 | ||||||
| chr7:151114303
|
G | A | 1 | a0001c0001t0001g0003 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.332-2490G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151114303 | ||||||
| chr7:151114361
|
T | A | 1 | a0001c0001t0001g0107 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.332-2432T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151114361 | ||||||
| chr7:151114643
|
G | C | 1 | a0001c0001t0001g0191 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.332-2150G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151114643 | ||||||
| chr7:151114697
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.332-2096C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151114697 | ||||||
| chr7:151114757
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.332-2036C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151114757 | ||||||
| chr7:151114779
|
G | C | 1 | a0001c0001t0002g0305 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.332-2014G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151114779 | ||||||
| chr7:151114983
|
C | A | 1 | a0001c0001t0001g0111 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.332-1810C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151114983 | ||||||
| chr7:151115176
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.332-1617G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115176 | ||||||
| chr7:151115399
|
G | A | 2 | a0001c0001t0003g0281a0001c0018t0001g0108 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.332-1394G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115399 | ||||||
| chr7:151115406
|
G | C | 304 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(301): Show | 313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.332-1387G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115406 | ||||||
| chr7:151115478
|
C | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0078others(12): Show | 16 | HG00140.hp1 HG00639.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.332-1315C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115478 | ||||||
| chr7:151115489
|
C | T | 1 | a0001c0001t0002g0305 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.332-1304C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115489 | ||||||
| chr7:151115565
|
G | A | 30 | a0001c0001t0001g0026a0001c0001t0001g0112a0001c0001t0001g0113others(27): Show | 33 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.332-1228G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115565 | ||||||
| chr7:151115596
|
G | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(84): Show | 90 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.332-1197G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115596 | ||||||
| chr7:151115652
|
G | C | 152 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(149): Show | 159 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.332-1141G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115652 | ||||||
| chr7:151115700
|
A | G | 155 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(152): Show | 162 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.332-1093A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115700 | ||||||
| chr7:151115708
|
A | G | 2 | a0001c0001t0001g0175a0001c0001t0002g0010 | 2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.332-1085A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115708 | ||||||
| chr7:151115773
|
C | T | 3 | a0001c0001t0001g0228a0001c0001t0001g0241a0001c0001t0002g0128 | 3 | HG00741.hp1 HG01106.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.332-1020C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115773 | ||||||
| chr7:151115928
|
C | T | 3 | a0001c0005t0006g0336a0001c0005t0006g0338a0001c0005t0006g0339 | 3 | HG02257.hp2 HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.332-865C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115928 | ||||||
| chr7:151115967
|
TGCTGTGG others(12): Show |
T | 1 | a0003c0019t0004g0292 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.332-825_332-807del others(19): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115967 | ||||||
| chr7:151116271
|
C | G | 137 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(134): Show | 144 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.332-522C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151116271 | ||||||
| chr7:151116282
|
GGGCCA | G | 3 | a0001c0001t0001g0247a0001c0001t0002g0297a0001c0001t0002g0298 | 3 | HG00735.hp2 HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.332-497_332-493del others(5): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151116282 | |||||
| chr7:151116307
|
C | T | 1 | a0001c0001t0003g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.332-486C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151116307 | ||||||
| chr7:151116314
|
C | G | 1 | a0001c0001t0001g0199 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.332-479C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151116314 | ||||||
| chr7:151116339
|
C | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0275 | 2 | NA18940.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.332-454C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151116339 | ||||||
| chr7:151116348
|
G | T | 4 | a0001c0003t0001g0027a0001c0003t0001g0134a0001c0003t0001g0135others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-445G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151116348 | ||||||
| chr7:151116451
|
G | A | 1 | a0001c0001t0006g0337 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.332-342G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151116451 | ||||||
| chr7:151116494
|
G | A | 2 | a0001c0007t0002g0316a0001c0007t0002g0320 | 2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.332-299G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151116494 | ||||||
| chr7:151116508
|
C | T | 1 | a0001c0004t0001g0013 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.332-285C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151116508 | ||||||
| chr7:151116890
|
T | TG | 74 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(71): Show | 78 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.390+46dupG | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 151116890 | |||||
| chr7:151117047
|
C | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0087 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.391-48C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 2/17 | chr7 | 151117047 | ||||||
| chr7:151117051
|
G | A | 20 | a0001c0001t0001g0125a0001c0001t0001g0133a0001c0001t0001g0279others(17): Show | 20 | HG01978.hp2 HG02257.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.391-44G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 2/17 | chr7 | 151117051 | ||||||
| chr7:151117253
|
T | TG | 7 | a0001c0001t0002g0296a0001c0001t0002g0306a0001c0001t0002g0308others(4): Show | 7 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.478+77dupG | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 151117253 | |||||
| chr7:151117476
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.564+20T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 4/17 | chr7 | 151117476 | ||||||
| chr7:151117485
|
A | G | 1 | a0001c0002t0002g0314 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.564+29A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 4/17 | chr7 | 151117485 | ||||||
| chr7:151117487
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.564+31C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 4/17 | chr7 | 151117487 | ||||||
| chr7:151117522
|
T | G | 1 | a0001c0001t0008g0022 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.564+66T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 4/17 | chr7 | 151117522 | ||||||
| chr7:151117587
|
A | G | 1 | a0001c0001t0002g0322 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.565-49A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 4/17 | chr7 | 151117587 | ||||||
| chr7:151117917
|
C | T | 2 | a0001c0007t0002g0316a0001c0007t0002g0320 | 2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.706+140C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/17 | chr7 | 151117917 | ||||||
| chr7:151117926
|
C | T | 1 | a0001c0001t0008g0022 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.706+149C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/17 | chr7 | 151117926 | ||||||
| chr7:151117952
|
G | A | 11 | a0001c0001t0002g0158a0001c0003t0001g0027a0001c0003t0001g0134others(8): Show | 11 | HG02055.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.706+175G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/17 | chr7 | 151117952 | ||||||
| chr7:151117975
|
G | C | 1 | a0001c0001t0001g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.706+198G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/17 | chr7 | 151117975 | ||||||
| chr7:151118190
|
C | T | 2 | a0001c0007t0002g0316a0001c0007t0002g0320 | 2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.707-20C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/17 | chr7 | 151118190 | ||||||
| chr7:151118483
|
T | C | 1 | a0001c0003t0001g0135 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.842-22T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 6/17 | chr7 | 151118483 | ||||||
| chr7:151118693
|
G | A | 1 | a0001c0018t0001g0108 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.969+61G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151118693 | ||||||
| chr7:151118702
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.969+70C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151118702 | ||||||
| chr7:151118795
|
C | T | 29 | a0001c0001t0001g0004a0001c0001t0001g0051a0001c0001t0001g0078others(26): Show | 30 | HG00140.hp1 HG00639.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.969+163C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151118795 | ||||||
| chr7:151118868
|
G | C | 1 | a0001c0001t0001g0114 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.969+236G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151118868 | ||||||
| chr7:151119070
|
G | T | 6 | a0001c0001t0001g0018a0001c0001t0001g0054a0001c0001t0001g0061others(3): Show | 6 | HG00735.hp1 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.969+438G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119070 | ||||||
| chr7:151119089
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.969+457G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119089 | ||||||
| chr7:151119138
|
T | C | 85 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0017others(82): Show | 86 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.969+506T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119138 | ||||||
| chr7:151119217
|
G | A | 1 | a0001c0001t0002g0148 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.969+585G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119217 | ||||||
| chr7:151119341
|
C | T | 91 | a0001c0001t0001g0004a0001c0001t0001g0051a0001c0001t0001g0078others(88): Show | 95 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.970-646C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119341 | ||||||
| chr7:151119346
|
C | T | 88 | a0001c0001t0001g0004a0001c0001t0001g0051a0001c0001t0001g0078others(85): Show | 92 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.970-641C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119346 | ||||||
| chr7:151119405
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.970-582T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119405 | ||||||
| chr7:151119426
|
C | T | 63 | a0001c0001t0001g0051a0001c0001t0001g0097a0001c0001t0001g0112others(60): Show | 66 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.970-561C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119426 | ||||||
| chr7:151119468
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.970-519C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119468 | ||||||
| chr7:151119528
|
G | A | 1 | a0001c0003t0006g0340 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.970-459G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119528 | ||||||
| chr7:151119540
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.970-447G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119540 | ||||||
| chr7:151119548
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.970-439C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119548 | ||||||
| chr7:151119555
|
C | T | 34 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(31): Show | 37 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.970-432C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119555 | ||||||
| chr7:151119639
|
C | T | 29 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0185others(26): Show | 29 | HG00423.hp1 HG00544.hp2 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.970-348C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119639 | ||||||
| chr7:151119760
|
C | T | 3 | a0001c0001t0002g0297a0001c0001t0002g0298a0001c0001t0002g0332 | 3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.970-227C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119760 | ||||||
| chr7:151119983
|
T | G | 1 | a0001c0001t0002g0322 | 1 | homoSapiens_chm13v2.hp1 | splice_region_variant&intron_variant | LOW | c.970-4T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119983 | ||||||
| chr7:151120228
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1128+83G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151120228 | ||||||
| chr7:151120273
|
C | T | 5 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1128+128C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151120273 | ||||||
| chr7:151120310
|
C | T | 1 | a0001c0001t0001g0006 | 2 | NA18947.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1128+165C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151120310 | ||||||
| chr7:151120374
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1128+229C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151120374 | ||||||
| chr7:151120722
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1128+577C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151120722 | ||||||
| chr7:151120917
|
C | T | 1 | a0001c0018t0001g0108 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1128+772C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151120917 | ||||||
| chr7:151120994
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1128+849C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151120994 | ||||||
| chr7:151121119
|
A | G | 82 | a0001c0001t0001g0004a0001c0001t0001g0078a0001c0001t0001g0083others(79): Show | 86 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1128+974A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121119 | ||||||
| chr7:151121162
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1128+1017C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121162 | ||||||
| chr7:151121215
|
C | T | 1 | a0001c0005t0006g0336 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1128+1070C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121215 | ||||||
| chr7:151121352
|
G | A | 2 | a0001c0001t0003g0209a0001c0001t0003g0276 | 2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1128+1207G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121352 | ||||||
| chr7:151121369
|
C | CCTG | 23 | a0001c0001t0001g0004a0001c0001t0001g0078a0001c0001t0001g0083others(20): Show | 24 | HG00140.hp1 HG00639.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.1128+1241_1128+124 others(7): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 151121369 | |||||
| chr7:151121433
|
T | C | 1 | a0001c0001t0001g0264 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1128+1288T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121433 | ||||||
| chr7:151121459
|
C | T | 1 | a0001c0002t0002g0321 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1128+1314C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121459 | ||||||
| chr7:151121462
|
C | T | 1 | a0001c0002t0002g0321 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1128+1317C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121462 | ||||||
| chr7:151121579
|
C | T | 37 | a0001c0001t0001g0004a0001c0001t0001g0078a0001c0001t0001g0083others(34): Show | 38 | HG00140.hp1 HG00639.hp2 HG01257.hp1 others(35): Show |
intron_variant | MODIFIER | c.1128+1434C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121579 | ||||||
| chr7:151121699
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1128+1554C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121699 | ||||||
| chr7:151121826
|
C | T | 38 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(35): Show | 41 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.1128+1681C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121826 | ||||||
| chr7:151121921
|
G | A | 30 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(27): Show | 33 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.1128+1776G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121921 | ||||||
| chr7:151122082
|
C | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(70): Show | 76 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1129-1712C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151122082 | ||||||
| chr7:151122230
|
C | T | 3 | a0001c0001t0002g0297a0001c0001t0002g0298a0001c0001t0002g0332 | 3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1129-1564C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151122230 | ||||||
| chr7:151122298
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1129-1496G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151122298 | ||||||
| chr7:151122311
|
G | A | 5 | a0001c0001t0002g0301a0001c0001t0002g0303a0001c0001t0002g0305others(2): Show | 5 | HG02735.hp1 HG03017.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.1129-1483G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151122311 | ||||||
| chr7:151122369
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1129-1425C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151122369 | ||||||
| chr7:151122453
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1129-1341C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151122453 | ||||||
| chr7:151122496
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1129-1298C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151122496 | ||||||
| chr7:151122497
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | NA18970.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1129-1297G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151122497 | ||||||
| chr7:151122504
|
C | CCCG | 39 | a0001c0001t0001g0004a0001c0001t0001g0078a0001c0001t0001g0101others(36): Show | 40 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(37): Show |
intron_variant | MODIFIER | c.1129-1275_1129-127 others(7): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 151122504 | |||||
| chr7:151122568
|
TCTC | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0239a0001c0001t0001g0247 | 3 | HG00735.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1129-1222_1129-122 others(7): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 151122568 | |||||
| chr7:151122610
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1129-1184C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151122610 | ||||||
| chr7:151123236
|
C | T | 1 | a0001c0002t0002g0317 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1129-558C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151123236 | ||||||
| chr7:151123926
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1221+40G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151123926 | ||||||
| chr7:151124074
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1221+188C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124074 | ||||||
| chr7:151124114
|
C | T | 2 | a0001c0001t0006g0337a0001c0001t0006g0341 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1221+228C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124114 | ||||||
| chr7:151124160
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1221+274G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124160 | ||||||
| chr7:151124257
|
A | C | 2 | a0001c0001t0006g0337a0001c0001t0006g0341 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1221+371A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124257 | ||||||
| chr7:151124398
|
C | T | 35 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(32): Show | 38 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.1221+512C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124398 | ||||||
| chr7:151124407
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1221+521C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124407 | ||||||
| chr7:151124408
|
G | A | 75 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0021others(72): Show | 76 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1221+522G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124408 | ||||||
| chr7:151124426
|
T | C | 1 | a0001c0001t0002g0140 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1221+540T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124426 | ||||||
| chr7:151124466
|
G | A | 15 | a0001c0001t0001g0084a0001c0001t0001g0110a0001c0001t0001g0111others(12): Show | 15 | HG00280.hp1 HG00323.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1221+580G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124466 | ||||||
| chr7:151124538
|
G | A | 2 | a0001c0001t0001g0081a0001c0004t0001g0014 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1221+652G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124538 | ||||||
| chr7:151124669
|
C | A | 1 | a0001c0001t0001g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1221+783C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124669 | ||||||
| chr7:151124720
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1221+834T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124720 | ||||||
| chr7:151124920
|
G | A | 53 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0056others(50): Show | 56 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.1221+1034G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124920 | ||||||
| chr7:151124998
|
G | A | 4 | a0001c0001t0001g0175a0001c0001t0002g0010a0001c0007t0002g0316others(1): Show | 4 | HG01884.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1221+1112G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124998 | ||||||
| chr7:151125105
|
C | T | 105 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(102): Show | 109 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1221+1219C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125105 | ||||||
| chr7:151125239
|
C | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 142 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1221+1353C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125239 | ||||||
| chr7:151125240
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1221+1354G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125240 | ||||||
| chr7:151125358
|
A | G | 130 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(127): Show | 136 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1221+1472A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125358 | ||||||
| chr7:151125364
|
G | A | 29 | a0001c0001t0001g0006a0001c0001t0001g0083a0001c0001t0001g0120others(26): Show | 30 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1221+1478G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125364 | ||||||
| chr7:151125412
|
CTTAGAG | C | 5 | a0001c0001t0001g0231a0001c0001t0001g0259a0001c0001t0001g0260others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1221+1531_1221+153 others(10): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151125412 | |||||
| chr7:151125451
|
A | C | 1 | a0001c0001t0002g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1221+1565A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125451 | ||||||
| chr7:151125512
|
T | A | 1 | a0005c0012t0002g0334 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1221+1626T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125512 | ||||||
| chr7:151125572
|
G | C | 340 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(337): Show | 349 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.1221+1686G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125572 | ||||||
| chr7:151125604
|
G | A | 3 | a0001c0001t0002g0297a0001c0001t0002g0298a0001c0001t0002g0332 | 3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1221+1718G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125604 | ||||||
| chr7:151125620
|
CTCT | C | 3 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0002g0295 | 3 | HG01167.hp1 HG01169.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1221+1740_1221+174 others(7): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151125620 | |||||
| chr7:151125657
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1221+1771C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125657 | ||||||
| chr7:151125667
|
C | G | 1 | a0001c0017t0001g0222 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1221+1781C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125667 | ||||||
| chr7:151125670
|
T | G | 1 | a0001c0001t0001g0265 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1221+1784T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125670 | ||||||
| chr7:151125678
|
C | T | 108 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(105): Show | 112 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1221+1792C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125678 | ||||||
| chr7:151125952
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1221+2066G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125952 | ||||||
| chr7:151126047
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0270 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1221+2161C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126047 | ||||||
| chr7:151126052
|
G | C | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(116): Show | 121 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1221+2166G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126052 | ||||||
| chr7:151126055
|
TGGGTG | T | 320 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(317): Show | 329 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.1221+2178_1221+218 others(9): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151126055 | |||||
| chr7:151126068
|
G | C | 1 | a0001c0001t0002g0138 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1221+2182G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126068 | ||||||
| chr7:151126087
|
TCGTTCCG others(21): Show |
T | 28 | a0001c0001t0001g0006a0001c0001t0001g0083a0001c0001t0001g0120others(25): Show | 29 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.1221+2205_1221+223 others(32): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151126087 | |||||
| chr7:151126140
|
TCCG | T | 35 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(32): Show | 38 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.1221+2257_1221+225 others(7): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151126140 | |||||
| chr7:151126202
|
C | T | 112 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0017others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1221+2316C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126202 | ||||||
| chr7:151126274
|
CGCCCTGA others(8): Show |
C | 40 | a0001c0001t0001g0007a0001c0001t0001g0112a0001c0001t0001g0113others(37): Show | 44 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.1222-2304_1222-229 others(19): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151126274 | |||||
| chr7:151126291
|
A | T | 40 | a0001c0001t0001g0007a0001c0001t0001g0112a0001c0001t0001g0113others(37): Show | 44 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.1222-2289A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126291 | ||||||
| chr7:151126356
|
GGAGCA | G | 310 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(307): Show | 319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.1222-2214_1222-221 others(9): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151126356 | |||||
| chr7:151126366
|
A | G | 3 | a0001c0001t0002g0297a0001c0001t0002g0298a0001c0001t0002g0332 | 3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1222-2214A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126366 | ||||||
| chr7:151126381
|
G | A | 3 | a0001c0005t0006g0336a0001c0005t0006g0338a0001c0005t0006g0339 | 3 | HG02257.hp2 HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1222-2199G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126381 | ||||||
| chr7:151126391
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1222-2189C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126391 | ||||||
| chr7:151126411
|
G | GAAGGCTG others(3): Show |
1 | a0001c0001t0001g0263 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1222-2168_1222-215 others(14): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151126411 | |||||
| chr7:151126412
|
A | AAGGCTGG others(13): Show |
3 | a0001c0001t0002g0297a0001c0001t0002g0298a0001c0001t0002g0332 | 3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1222-2159_1222-215 others(24): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151126412 | |||||
| chr7:151126412
|
AAGGCTGG others(3): Show |
A | 139 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(136): Show | 143 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1222-2124_1222-211 others(14): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151126412 | |||||
| chr7:151126412
|
AAGGCTGG others(13): Show |
A | 1 | a0001c0001t0001g0111 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1222-2134_1222-211 others(24): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151126412 | |||||
| chr7:151126422
|
G | A | 157 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(154): Show | 162 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1222-2158G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126422 | ||||||
| chr7:151126432
|
G | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(135): Show | 142 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1222-2148G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126432 | ||||||
| chr7:151126442
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1222-2138G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126442 | ||||||
| chr7:151126444
|
G | A | 3 | a0001c0001t0002g0297a0001c0001t0002g0298a0001c0001t0002g0332 | 3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1222-2136G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126444 | ||||||
| chr7:151126483
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1222-2097G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126483 | ||||||
| chr7:151126535
|
T | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(136): Show | 143 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1222-2045T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126535 | ||||||
| chr7:151126625
|
C | T | 28 | a0001c0001t0001g0006a0001c0001t0001g0083a0001c0001t0001g0120others(25): Show | 29 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.1222-1955C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126625 | ||||||
| chr7:151126633
|
C | A | 1 | a0001c0001t0002g0330 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1222-1947C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126633 | ||||||
| chr7:151126675
|
T | C | 4 | a0001c0001t0001g0175a0001c0001t0002g0010a0001c0007t0002g0316others(1): Show | 4 | HG01884.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222-1905T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126675 | ||||||
| chr7:151126794
|
C | T | 3 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0002g0295 | 3 | HG01167.hp1 HG01169.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1222-1786C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126794 | ||||||
| chr7:151126897
|
C | T | 4 | a0001c0001t0001g0175a0001c0001t0002g0010a0001c0007t0002g0316others(1): Show | 4 | HG01884.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222-1683C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126897 | ||||||
| chr7:151126926
|
C | T | 4 | a0001c0001t0001g0175a0001c0001t0002g0010a0001c0007t0002g0316others(1): Show | 4 | HG01884.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222-1654C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126926 | ||||||
| chr7:151126934
|
C | T | 40 | a0001c0001t0001g0007a0001c0001t0001g0112a0001c0001t0001g0113others(37): Show | 44 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.1222-1646C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126934 | ||||||
| chr7:151126988
|
A | T | 5 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0080others(2): Show | 5 | HG02717.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222-1592A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126988 | ||||||
| chr7:151126997
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1222-1583C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126997 | ||||||
| chr7:151127066
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1222-1514C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127066 | ||||||
| chr7:151127138
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1222-1442G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127138 | ||||||
| chr7:151127155
|
G | A | 1 | a0001c0001t0002g0322 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1222-1425G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127155 | ||||||
| chr7:151127247
|
G | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0002g0145 | 3 | HG00544.hp2 HG02083.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1222-1333G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127247 | ||||||
| chr7:151127257
|
G | A | 140 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(137): Show | 144 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.1222-1323G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127257 | ||||||
| chr7:151127383
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0051others(35): Show | 39 | HG00140.hp1 HG01109.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.1222-1197G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127383 | ||||||
| chr7:151127421
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1222-1159C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127421 | ||||||
| chr7:151127426
|
T | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0201a0001c0001t0001g0238others(2): Show | 6 | HG02015.hp2 HG02080.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1222-1154T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127426 | ||||||
| chr7:151127648
|
C | T | 40 | a0001c0001t0001g0007a0001c0001t0001g0112a0001c0001t0001g0113others(37): Show | 44 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.1222-932C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127648 | ||||||
| chr7:151127784
|
C | T | 118 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0017others(115): Show | 119 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1222-796C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127784 | ||||||
| chr7:151127826
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1222-754G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127826 | ||||||
| chr7:151127944
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1222-636C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127944 | ||||||
| chr7:151127945
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1222-635G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127945 | ||||||
| chr7:151127950
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1222-630T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127950 | ||||||
| chr7:151128000
|
G | A | 258 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(255): Show | 263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1222-580G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151128000 | ||||||
| chr7:151128009
|
G | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(65): Show | 70 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1222-571G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151128009 | ||||||
| chr7:151128228
|
G | A | 112 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0017others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1222-352G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151128228 | ||||||
| chr7:151128263
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1222-317T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151128263 | ||||||
| chr7:151128272
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1222-308C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151128272 | ||||||
| chr7:151128307
|
T | A | 1 | a0001c0001t0002g0109 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1222-273T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151128307 | ||||||
| chr7:151128405
|
A | G | 121 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0017others(118): Show | 122 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1222-175A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151128405 | ||||||
| chr7:151128480
|
C | G | 1 | a0001c0001t0001g0224 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1222-100C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151128480 | ||||||
| chr7:151128480
|
C | T | 257 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(254): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1222-100C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151128480 | ||||||
| chr7:151128719
|
T | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0056 | 3 | HG03098.hp1 HG03579.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1326+35T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151128719 | ||||||
| chr7:151128752
|
G | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0017others(102): Show | 106 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.1326+68G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151128752 | ||||||
| chr7:151128778
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1326+94C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151128778 | ||||||
| chr7:151128846
|
G | T | 1 | a0001c0018t0001g0108 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1326+162G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151128846 | ||||||
| chr7:151128852
|
C | G | 2 | a0001c0001t0001g0127a0001c0001t0002g0157 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1326+168C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151128852 | ||||||
| chr7:151128948
|
A | C | 37 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0051others(34): Show | 38 | HG00140.hp1 HG01109.hp1 HG01257.hp1 others(35): Show |
intron_variant | MODIFIER | c.1326+264A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151128948 | ||||||
| chr7:151128957
|
G | A | 300 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(297): Show | 309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.1326+273G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151128957 | ||||||
| chr7:151129132
|
C | G | 40 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0051others(37): Show | 41 | HG00140.hp1 HG01109.hp1 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.1326+448C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129132 | ||||||
| chr7:151129231
|
C | T | 100 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(97): Show | 103 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1326+547C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129231 | ||||||
| chr7:151129258
|
C | T | 2 | a0001c0001t0006g0337a0001c0001t0006g0341 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1326+574C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129258 | ||||||
| chr7:151129298
|
A | G | 120 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0017others(117): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1326+614A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129298 | ||||||
| chr7:151129319
|
C | G | 119 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0017others(116): Show | 120 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1326+635C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129319 | ||||||
| chr7:151129330
|
G | A | 1 | a0001c0001t0006g0337 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1326+646G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129330 | ||||||
| chr7:151129458
|
C | G | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(146): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1326+774C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129458 | ||||||
| chr7:151129462
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1326+778G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129462 | ||||||
| chr7:151129468
|
A | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(105): Show | 112 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1326+784A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129468 | ||||||
| chr7:151129474
|
C | T | 4 | a0001c0001t0001g0020a0001c0001t0001g0247a0001c0001t0002g0159others(1): Show | 4 | HG00735.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1326+790C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129474 | ||||||
| chr7:151129710
|
G | A | 1 | a0001c0001t0001g0040 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1326+1026G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129710 | ||||||
| chr7:151129731
|
CTCGCGAG | C | 35 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(32): Show | 38 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.1326+1050_1326+105 others(11): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 151129731 | |||||
| chr7:151129825
|
G | A | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(141): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.1326+1141G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129825 | ||||||
| chr7:151129910
|
C | T | 1 | a0001c0001t0002g0307 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1326+1226C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129910 | ||||||
| chr7:151130017
|
G | A | 13 | a0001c0001t0001g0084a0001c0001t0001g0110a0001c0001t0001g0111others(10): Show | 13 | HG00280.hp1 HG00323.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1326+1333G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130017 | ||||||
| chr7:151130050
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1326+1366G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130050 | ||||||
| chr7:151130120
|
A | G | 320 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(317): Show | 329 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.1326+1436A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130120 | ||||||
| chr7:151130246
|
G | A | 2 | a0001c0001t0001g0259a0001c0001t0002g0167 | 2 | HG01243.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1326+1562G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130246 | ||||||
| chr7:151130249
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0002g0157 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1326+1565G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130249 | ||||||
| chr7:151130587
|
C | T | 4 | a0001c0001t0001g0185a0001c0001t0001g0205a0001c0001t0001g0211others(1): Show | 4 | HG02132.hp1 NA18962.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1326+1903C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130587 | ||||||
| chr7:151130715
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0002g0157 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1326+2031G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130715 | ||||||
| chr7:151130773
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1326+2089C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130773 | ||||||
| chr7:151130839
|
T | A | 1 | a0001c0001t0001g0215 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1326+2155T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130839 | ||||||
| chr7:151130864
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1326+2180C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130864 | ||||||
| chr7:151130972
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1326+2288T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130972 | ||||||
| chr7:151131017
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1326+2333G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131017 | ||||||
| chr7:151131082
|
G | A | 4 | a0001c0001t0001g0260a0001c0002t0002g0314a0001c0004t0001g0013others(1): Show | 4 | HG02055.hp1 HG02886.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326+2398G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131082 | ||||||
| chr7:151131132
|
C | T | 1 | a0001c0001t0002g0178 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1326+2448C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131132 | ||||||
| chr7:151131229
|
A | G | 58 | a0001c0001t0001g0007a0001c0001t0001g0107a0001c0001t0001g0112others(55): Show | 62 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1326+2545A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131229 | ||||||
| chr7:151131385
|
C | T | 1 | a0001c0001t0004g0253 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1326+2701C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131385 | ||||||
| chr7:151131432
|
A | T | 1 | a0001c0001t0007g0172 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1326+2748A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131432 | ||||||
| chr7:151131437
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1326+2753C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131437 | ||||||
| chr7:151131494
|
A | G | 10 | a0001c0001t0001g0107a0001c0001t0001g0133a0001c0002t0002g0310others(7): Show | 10 | HG01884.hp2 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1326+2810A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131494 | ||||||
| chr7:151131559
|
C | T | 4 | a0001c0003t0001g0134a0001c0003t0001g0135a0001c0003t0001g0137others(1): Show | 4 | HG02055.hp2 HG02258.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1327-2841C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131559 | ||||||
| chr7:151131589
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1327-2811T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131589 | ||||||
| chr7:151131605
|
G | C | 1 | a0001c0001t0001g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1327-2795G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131605 | ||||||
| chr7:151131995
|
G | A | 1 | a0001c0001t0002g0155 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1327-2405G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131995 | ||||||
| chr7:151132014
|
G | T | 2 | a0001c0001t0003g0104a0001c0001t0003g0281 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1327-2386G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132014 | ||||||
| chr7:151132134
|
G | C | 291 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(288): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.1327-2266G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132134 | ||||||
| chr7:151132135
|
G | A | 17 | a0001c0001t0001g0006a0001c0001t0001g0177a0001c0001t0001g0199others(14): Show | 18 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.1327-2265G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132135 | ||||||
| chr7:151132371
|
A | G | 313 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(310): Show | 322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.1327-2029A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132371 | ||||||
| chr7:151132374
|
C | G | 1 | a0001c0001t0001g0215 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1327-2026C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132374 | ||||||
| chr7:151132407
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1327-1993G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132407 | ||||||
| chr7:151132428
|
T | C | 1 | a0001c0001t0001g0215 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1327-1972T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132428 | ||||||
| chr7:151132549
|
G | A | 4 | a0001c0001t0001g0175a0001c0001t0002g0010a0001c0007t0002g0316others(1): Show | 4 | HG01884.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1327-1851G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132549 | ||||||
| chr7:151132570
|
A | G | 2 | a0001c0002t0002g0314a0001c0004t0001g0013 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1327-1830A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132570 | ||||||
| chr7:151132595
|
G | A | 1 | a0001c0001t0002g0327 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1327-1805G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132595 | ||||||
| chr7:151132602
|
C | T | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0239 | 3 | HG02896.hp2 HG02897.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1327-1798C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132602 | ||||||
| chr7:151132622
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1327-1778G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132622 | ||||||
| chr7:151132741
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1327-1659G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132741 | ||||||
| chr7:151132849
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1327-1551C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132849 | ||||||
| chr7:151132928
|
A | G | 155 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(152): Show | 162 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1327-1472A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132928 | ||||||
| chr7:151132934
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1327-1466C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132934 | ||||||
| chr7:151132947
|
G | A | 4 | a0001c0001t0001g0174a0001c0001t0001g0202a0001c0001t0001g0203others(1): Show | 4 | HG02896.hp2 HG02897.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1327-1453G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132947 | ||||||
| chr7:151133037
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1327-1363C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133037 | ||||||
| chr7:151133064
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1327-1336C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133064 | ||||||
| chr7:151133134
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1327-1266A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133134 | ||||||
| chr7:151133204
|
A | C | 10 | a0001c0001t0001g0125a0001c0001t0001g0133a0001c0002t0002g0310others(7): Show | 10 | HG01884.hp2 HG01978.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1327-1196A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133204 | ||||||
| chr7:151133254
|
G | A | 3 | a0001c0001t0001g0214a0001c0001t0001g0263a0001c0001t0002g0322 | 3 | HG01255.hp1 HG02145.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1327-1146G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133254 | ||||||
| chr7:151133476
|
G | A | 2 | a0001c0001t0003g0104a0001c0001t0003g0281 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1327-924G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133476 | ||||||
| chr7:151133507
|
G | A | 3 | a0001c0001t0001g0083a0001c0001t0001g0120a0001c0001t0001g0125 | 3 | HG00639.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1327-893G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133507 | ||||||
| chr7:151133719
|
C | T | 10 | a0001c0001t0001g0045a0001c0001t0001g0179a0001c0001t0001g0197others(7): Show | 10 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.1327-681C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133719 | ||||||
| chr7:151133798
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1327-602C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133798 | ||||||
| chr7:151133801
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1327-599C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133801 | ||||||
| chr7:151133912
|
G | A | 1 | a0001c0001t0004g0271 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1327-488G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133912 | ||||||
| chr7:151133945
|
G | A | 4 | a0001c0001t0001g0026a0001c0001t0001g0136a0001c0001t0002g0313others(1): Show | 4 | HG01891.hp1 HG01952.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1327-455G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133945 | ||||||
| chr7:151134013
|
C | A | 36 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(33): Show | 39 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1327-387C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151134013 | ||||||
| chr7:151134025
|
C | T | 1 | a0001c0002t0002g0312 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1327-375C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151134025 | ||||||
| chr7:151134135
|
T | C | 40 | a0001c0001t0001g0006a0001c0001t0001g0083a0001c0001t0001g0107others(37): Show | 41 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1327-265T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151134135 | ||||||
| chr7:151134142
|
C | T | 1 | a0001c0001t0002g0333 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1327-258C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151134142 | ||||||
| chr7:151134202
|
C | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0078a0001c0001t0001g0116others(20): Show | 24 | HG00140.hp1 HG01109.hp1 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.1327-198C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151134202 | ||||||
| chr7:151134231
|
C | T | 7 | a0001c0001t0001g0182a0001c0001t0001g0192a0001c0001t0001g0257others(4): Show | 7 | NA18959.hp1 NA18975.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.1327-169C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151134231 | ||||||
| chr7:151134256
|
A | G | 45 | a0001c0001t0001g0007a0001c0001t0001g0112a0001c0001t0001g0113others(42): Show | 49 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1327-144A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151134256 | ||||||
| chr7:151134276
|
G | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0220a0001c0001t0001g0240 | 3 | HG03490.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1327-124G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151134276 | ||||||
| chr7:151134344
|
C | T | 8 | a0001c0001t0001g0180a0001c0001t0001g0184a0001c0001t0001g0189others(5): Show | 8 | HG00280.hp1 HG00323.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1327-56C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151134344 | ||||||
| chr7:151134575
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0231 | 2 | HG03486.hp1 NA19010.hp1 |
splice_region_variant&intron_variant | LOW | c.1495+7C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151134575 | ||||||
| chr7:151134677
|
G | A | 10 | a0001c0001t0001g0107a0001c0001t0001g0133a0001c0002t0002g0310others(7): Show | 10 | HG01884.hp2 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1495+109G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151134677 | ||||||
| chr7:151134685
|
C | T | 3 | a0001c0001t0002g0297a0001c0001t0002g0298a0001c0001t0002g0332 | 3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1495+117C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151134685 | ||||||
| chr7:151134721
|
C | G | 1 | a0001c0007t0002g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1495+153C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151134721 | ||||||
| chr7:151134721
|
C | T | 48 | a0001c0001t0001g0007a0001c0001t0001g0112a0001c0001t0001g0113others(45): Show | 52 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1495+153C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151134721 | ||||||
| chr7:151134793
|
G | T | 4 | a0001c0001t0001g0175a0001c0001t0002g0010a0001c0007t0002g0316others(1): Show | 4 | HG01884.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1495+225G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151134793 | ||||||
| chr7:151134901
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0270 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1495+333G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151134901 | ||||||
| chr7:151134950
|
C | T | 4 | a0001c0001t0001g0175a0001c0001t0002g0010a0001c0007t0002g0316others(1): Show | 4 | HG01884.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1495+382C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151134950 | ||||||
| chr7:151134965
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1495+397T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151134965 | ||||||
| chr7:151135130
|
A | T | 2 | a0001c0001t0006g0337a0001c0001t0006g0341 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1495+562A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151135130 | ||||||
| chr7:151135195
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1495+627G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151135195 | ||||||
| chr7:151135699
|
G | A | 29 | a0001c0001t0001g0006a0001c0001t0001g0083a0001c0001t0001g0120others(26): Show | 30 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1495+1131G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151135699 | ||||||
| chr7:151135826
|
A | G | 308 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(305): Show | 317 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.1495+1258A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151135826 | ||||||
| chr7:151135836
|
A | G | 45 | a0001c0001t0001g0007a0001c0001t0001g0112a0001c0001t0001g0113others(42): Show | 49 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1495+1268A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151135836 | ||||||
| chr7:151135872
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1495+1304A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151135872 | ||||||
| chr7:151135906
|
A | C | 67 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0025others(64): Show | 71 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1495+1338A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151135906 | ||||||
| chr7:151136083
|
T | G | 1 | a0001c0001t0001g0050 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1495+1515T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136083 | ||||||
| chr7:151136256
|
C | A | 1 | a0001c0001t0002g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1495+1688C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136256 | ||||||
| chr7:151136380
|
C | A | 2 | a0001c0001t0001g0194a0001c0001t0001g0254 | 2 | HG00280.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1496-1763C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136380 | ||||||
| chr7:151136384
|
C | T | 1 | a0001c0001t0003g0104 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1496-1759C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136384 | ||||||
| chr7:151136418
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1496-1725C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136418 | ||||||
| chr7:151136440
|
G | A | 1 | a0001c0001t0006g0341 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1496-1703G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136440 | ||||||
| chr7:151136711
|
C | T | 9 | a0001c0001t0001g0250a0001c0002t0002g0310a0001c0002t0002g0311others(6): Show | 9 | HG01884.hp2 HG02132.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1496-1432C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136711 | ||||||
| chr7:151136853
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1496-1290A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136853 | ||||||
| chr7:151136921
|
G | GGGCAGCG others(27): Show |
1 | a0001c0001t0001g0099 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1496-1221_1496-122 others(38): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 151136921 | |||||
| chr7:151136933
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1496-1210A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136933 | ||||||
| chr7:151136950
|
G | T | 1 | a0001c0001t0001g0099 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1496-1193G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136950 | ||||||
| chr7:151136983
|
C | G | 1 | a0001c0001t0001g0099 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1496-1160C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136983 | ||||||
| chr7:151136984
|
A | T | 1 | a0001c0001t0001g0099 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1496-1159A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136984 | ||||||
| chr7:151136997
|
A | T | 1 | a0001c0001t0001g0099 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1496-1146A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136997 | ||||||
| chr7:151136998
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1496-1145G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136998 | ||||||
| chr7:151137001
|
C | A | 1 | a0001c0001t0001g0099 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1496-1142C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137001 | ||||||
| chr7:151137002
|
T | G | 1 | a0001c0001t0001g0099 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1496-1141T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137002 | ||||||
| chr7:151137079
|
G | A | 1 | a0001c0001t0002g0329 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1496-1064G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137079 | ||||||
| chr7:151137261
|
C | T | 1 | a0001c0002t0002g0317 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1496-882C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137261 | ||||||
| chr7:151137360
|
G | A | 5 | a0001c0001t0002g0301a0001c0003t0001g0134a0001c0003t0001g0135others(2): Show | 5 | HG02055.hp2 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1496-783G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137360 | ||||||
| chr7:151137429
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0229a0001c0001t0001g0290 | 4 | HG03017.hp1 HG03688.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1496-714G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137429 | ||||||
| chr7:151137452
|
C | T | 74 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0083others(71): Show | 75 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.1496-691C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137452 | ||||||
| chr7:151137536
|
G | A | 40 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(37): Show | 42 | HG00140.hp2 HG01081.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.1496-607G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137536 | ||||||
| chr7:151137600
|
T | C | 16 | a0001c0001t0001g0056a0001c0001t0001g0098a0001c0001t0001g0114others(13): Show | 16 | HG00438.hp1 HG01884.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1496-543T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137600 | ||||||
| chr7:151137640
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1496-503C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137640 | ||||||
| chr7:151137750
|
G | A | 2 | a0001c0001t0001g0125a0001c0003t0006g0340 | 2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1496-393G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137750 | ||||||
| chr7:151137825
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1496-318C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137825 | ||||||
| chr7:151138123
|
C | T | 1 | a0001c0018t0001g0108 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1496-20C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151138123 | ||||||
| chr7:151138724
|
C | T | 3 | a0001c0001t0001g0051a0001c0001t0001g0097a0001c0001t0001g0130 | 3 | NA18951.hp1 NA18989.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1666+411C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151138724 | ||||||
| chr7:151138761
|
T | C | 6 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG02486.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1666+448T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151138761 | ||||||
| chr7:151138782
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1666+469C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151138782 | ||||||
| chr7:151138783
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1666+470G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151138783 | ||||||
| chr7:151138860
|
T | C | 1 | a0001c0001t0002g0309 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1666+547T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151138860 | ||||||
| chr7:151138875
|
A | C | 2 | a0001c0001t0003g0104a0001c0001t0003g0281 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1666+562A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151138875 | ||||||
| chr7:151138898
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1666+585G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151138898 | ||||||
| chr7:151139005
|
CCCTACTT others(6): Show |
C | 1 | a0001c0001t0001g0047 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1666+693_1666+705d others(15): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139005 | ||||||
| chr7:151139153
|
A | G | 89 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 95 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1667-826A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139153 | ||||||
| chr7:151139270
|
C | T | 1 | a0007c0014t0001g0033 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1667-709C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139270 | ||||||
| chr7:151139520
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1667-459G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139520 | ||||||
| chr7:151139522
|
C | A | 1 | a0007c0014t0001g0033 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1667-457C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139522 | ||||||
| chr7:151139522
|
C | T | 1 | a0001c0001t0006g0341 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1667-457C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139522 | ||||||
| chr7:151139540
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1667-439C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139540 | ||||||
| chr7:151139640
|
A | C | 1 | a0001c0001t0001g0231 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1667-339A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139640 | ||||||
| chr7:151139833
|
G | A | 3 | a0001c0001t0001g0175a0001c0001t0002g0010a0001c0007t0002g0316 | 3 | HG01884.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1667-146G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139833 | ||||||
| chr7:151139840
|
G | C | 1 | a0001c0001t0002g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1667-139G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139840 | ||||||
| chr7:151139921
|
G | A | 4 | a0001c0001t0001g0260a0001c0004t0001g0016a0001c0005t0006g0336others(1): Show | 4 | HG02055.hp1 HG02280.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1667-58G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139921 | ||||||
| chr7:151139963
|
A | C | 1 | a0001c0001t0001g0092 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1667-16A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139963 | ||||||
| chr7:151140139
|
C | T | 1 | a0001c0001t0006g0341 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1804+23C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 13/17 | chr7 | 151140139 | ||||||
| chr7:151140428
|
C | T | 18 | a0001c0001t0001g0045a0001c0001t0001g0123a0001c0001t0001g0131others(15): Show | 18 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.1804+312C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 13/17 | chr7 | 151140428 | ||||||
| chr7:151140442
|
C | T | 112 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0017others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1804+326C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 13/17 | chr7 | 151140442 | ||||||
| chr7:151140951
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0279 | 2 | HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1804+835C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 13/17 | chr7 | 151140951 | ||||||
| chr7:151141079
|
C | T | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0239 | 3 | HG02896.hp2 HG02897.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1805-819C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 13/17 | chr7 | 151141079 | ||||||
| chr7:151141136
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1805-762C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 13/17 | chr7 | 151141136 | ||||||
| chr7:151141607
|
A | T | 4 | a0001c0001t0001g0080a0001c0001t0001g0175a0001c0001t0002g0010others(1): Show | 4 | HG01884.hp1 HG03195.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1805-291A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 13/17 | chr7 | 151141607 | ||||||
| chr7:151142269
|
G | T | 1 | a0001c0001t0001g0071 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2050+16G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 15/17 | chr7 | 151142269 | ||||||
| chr7:151142655
|
A | T | 1 | a0001c0001t0001g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2273+21A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 16/17 | chr7 | 151142655 | ||||||
| chr7:151142677
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0056others(2): Show | 5 | HG02717.hp1 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2273+43C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 16/17 | chr7 | 151142677 | ||||||
| chr7:151142706
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2273+72G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 16/17 | chr7 | 151142706 | ||||||
| chr7:151142837
|
C | T | 1 | a0006c0015t0001g0124 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2273+203C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 16/17 | chr7 | 151142837 | ||||||
| chr7:151143176
|
G | C | 3 | a0001c0001t0001g0011a0001c0001t0002g0159a0001c0001t0006g0337 | 3 | HG02451.hp1 HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2274-165G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 16/17 | chr7 | 151143176 | ||||||
| chr7:151143200
|
C | T | 4 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2274-141C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 16/17 | chr7 | 151143200 |