Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8540 |
|---|---|
| ensemblid | ENSG00000018510.18 |
| hgncid | 327 |
| symbol | AGPS |
| name | alkylglycerone phosphate synthase |
| refseq_nuc | NM_003659.4 |
| refseq_prot | NP_003650.1 |
| ensembl_nuc | ENST00000264167.11 |
| ensembl_prot | ENSP00000264167.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 177392773 |
| end | 177543834 |
| strand | + |
| ver | v1.2 |
| region | chr2:177392773-177543834 |
| region5000 | chr2:177387773-177548834 |
| regionname0 | AGPS_chr2_177392773_177543834 |
| regionname5000 | AGPS_chr2_177387773_177548834 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 658 | 258 | 78 | 40 | 114 | 2 | 22 | 90 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1977 | 239 | 65 | 40 | 114 | 2 | 17 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| c0002 | 0/1 | 1977 | 15 | 9 | 0 | 0 | 0 | 5 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| c0003 | 0/0 | 1977 | 3 | 3 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| c0004 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| 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 | 5658 | 82 | 15 | 16 | 40 | 2 | 9 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0002 | 0/0 | 5656 | 50 | 1 | 7 | 37 | 0 | 5 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0003 | 1/0 | 5657 | 14 | 10 | 2 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0004 | 0/1 | 5652 | 12 | 7 | 0 | 0 | 0 | 4 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0005 | 0/0 | 5662 | 10 | 9 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0006 | 0/0 | 5656 | 7 | 0 | 0 | 7 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0007 | 0/0 | 5656 | 6 | 0 | 0 | 6 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0008 | 0/0 | 5652 | 5 | 4 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0009 | 0/0 | 5660 | 5 | 1 | 1 | 2 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0010 | 0/0 | 5656 | 4 | 0 | 1 | 3 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0011 | 0/0 | 5660 | 4 | 0 | 0 | 4 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0012 | 0/0 | 5666 | 3 | 3 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0013 | 0/0 | 5662 | 3 | 2 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0014 | 0/0 | 5656 | 3 | 3 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0015 | 0/0 | 5649 | 3 | 0 | 2 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0016 | 0/0 | 5655 | 3 | 3 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0017 | 0/0 | 5656 | 2 | 2 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0018 | 0/0 | 5654 | 2 | 1 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0019 | 0/0 | 5664 | 2 | 2 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0020 | 0/0 | 5658 | 2 | 1 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0021 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0022 | 0/0 | 5660 | 2 | 0 | 0 | 2 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0023 | 0/0 | 5657 | 2 | 0 | 2 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0024 | 0/0 | 5658 | 2 | 1 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0025 | 0/0 | 5652 | 2 | 2 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0026 | 0/0 | 5657 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0027 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0028 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0029 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0030 | 0/0 | 5657 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0031 | 0/0 | 5660 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0032 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0033 | 0/0 | 5662 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0034 | 0/0 | 5656 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0035 | 0/0 | 5660 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0036 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0037 | 0/0 | 5662 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0038 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0039 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0040 | 0/0 | 5656 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0041 | 0/0 | 5668 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0042 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0043 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0044 | 0/0 | 5656 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0045 | 0/0 | 5608 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0046 | 0/0 | 5656 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0047 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0048 | 0/0 | 5652 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0049 | 0/0 | 5655 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0050 | 0/0 | 5655 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| t0051 | 0/0 | 5649 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0010 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1977 | 239 | 65 | 40 | 114 | 2 | 17 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0002 | 0/1 | 1977 | 15 | 9 | 0 | 0 | 0 | 5 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0003 | 0/0 | 1977 | 3 | 3 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0004 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7634 | 81 | 14 | 16 | 40 | 2 | 9 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0002 | 0/0 | 7632 | 50 | 1 | 7 | 37 | 0 | 5 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0003 | 1/0 | 7633 | 14 | 10 | 2 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0004 | 0/0 | 7628 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0005 | 0/0 | 7638 | 8 | 7 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0006 | 0/0 | 7632 | 7 | 0 | 0 | 7 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0007 | 0/0 | 7632 | 6 | 0 | 0 | 6 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0008 | 0/0 | 7628 | 5 | 4 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0009 | 0/0 | 7636 | 4 | 0 | 1 | 2 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0010 | 0/0 | 7632 | 4 | 0 | 1 | 3 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0011 | 0/0 | 7636 | 4 | 0 | 0 | 4 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0012 | 0/0 | 7642 | 3 | 3 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0013 | 0/0 | 7638 | 2 | 1 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0014 | 0/0 | 7632 | 3 | 3 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0015 | 0/0 | 7625 | 3 | 0 | 2 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0016 | 0/0 | 7631 | 3 | 3 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0017 | 0/0 | 7632 | 2 | 2 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0018 | 0/0 | 7630 | 2 | 1 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0019 | 0/0 | 7640 | 2 | 2 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0020 | 0/0 | 7634 | 2 | 1 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0021 | 0/0 | 7634 | 2 | 0 | 0 | 2 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0022 | 0/0 | 7636 | 2 | 0 | 0 | 2 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0023 | 0/0 | 7633 | 2 | 0 | 2 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0024 | 0/0 | 7634 | 2 | 1 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0025 | 0/0 | 7628 | 2 | 2 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0026 | 0/0 | 7633 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0027 | 0/0 | 7633 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0028 | 0/0 | 7633 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0029 | 0/0 | 7634 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0030 | 0/0 | 7633 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0032 | 0/0 | 7640 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0033 | 0/0 | 7638 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0035 | 0/0 | 7636 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0036 | 0/0 | 7634 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0037 | 0/0 | 7638 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0038 | 0/0 | 7634 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0039 | 0/0 | 7634 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0040 | 0/0 | 7632 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0041 | 0/0 | 7644 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0042 | 0/0 | 7634 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0043 | 0/0 | 7634 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0044 | 0/0 | 7632 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0045 | 0/0 | 7584 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0046 | 0/0 | 7632 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0047 | 0/0 | 7634 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0049 | 0/0 | 7631 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0050 | 0/0 | 7631 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0001t0051 | 0/0 | 7625 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0002t0004 | 0/1 | 7628 | 11 | 6 | 0 | 0 | 0 | 4 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0002t0009 | 0/0 | 7636 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0002t0013 | 0/0 | 7638 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0002t0034 | 0/0 | 7632 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0002t0048 | 0/0 | 7628 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0003t0001 | 0/0 | 7634 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0003t0005 | 0/0 | 7638 | 2 | 2 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| a0001c0004t0031 | 0/0 | 7636 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | copy fasta | chr2 | 177387773 | 177548834 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0003g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0005g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0006g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0006g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0006g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0007g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0007g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0008g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0008g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0008g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0008g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0008g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0009g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0009g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0009g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0009g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0010g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0010g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0010g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0010g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0011g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0011g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0011g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0011g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0012g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0012g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0012g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0013g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0013g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0014g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0014g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0014g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0015g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0015g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0015g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0016g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0016g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0016g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0017g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0017g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0018g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0018g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0019g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0019g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0020g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0020g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0021g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0021g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0022g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0022g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0023g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0023g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0024g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0024g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0025g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0025g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0026g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0027g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0028g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0029g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0030g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0032g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0033g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0035g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0036g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0037g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0038g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0039g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0040g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0041g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0042g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0043g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0044g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0045g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0046g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0047g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0049g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0050g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0001t0051g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0002t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0002t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0002t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0002t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0002t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0002t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0002t0004g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0002t0004g0010 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0002t0004g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0002t0004g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0002t0004g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0002t0009g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0002t0013g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0002t0034g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0002t0048g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0003t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0003t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0003t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| a0001c0004t0031g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | CHS | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00438 | hp1 | a0001 | c0001 | t0021 | g0027 | EAS | CHS | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00544 | hp1 | a0001 | c0001 | t0006 | g0045 | EAS | CHS | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00544 | hp2 | a0001 | c0001 | t0010 | g0205 | EAS | CHS | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00558 | hp2 | a0001 | c0001 | t0007 | g0065 | EAS | CHS | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00597 | hp1 | a0001 | c0001 | t0010 | g0147 | EAS | CHS | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00597 | hp2 | a0001 | c0001 | t0006 | g0073 | EAS | CHS | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00609 | hp2 | a0001 | c0001 | t0007 | g0063 | EAS | CHS | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00673 | hp1 | a0001 | c0001 | t0007 | g0077 | EAS | CHS | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00673 | hp2 | a0001 | c0001 | t0022 | g0134 | EAS | CHS | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0200 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01074 | hp1 | a0001 | c0001 | t0040 | g0040 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01109 | hp1 | a0001 | c0001 | t0018 | g0215 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0091 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01167 | hp1 | a0001 | c0001 | t0044 | g0149 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01167 | hp2 | a0001 | c0001 | t0015 | g0223 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01168 | hp2 | a0001 | c0001 | t0026 | g0236 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01169 | hp1 | a0001 | c0001 | t0015 | g0224 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01175 | hp1 | a0001 | c0001 | t0010 | g0170 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01175 | hp2 | a0001 | c0001 | t0051 | g0228 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0217 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01255 | hp1 | a0001 | c0001 | t0030 | g0244 | AMR | CLM | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01256 | hp2 | a0001 | c0001 | t0023 | g0074 | AMR | CLM | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | CLM | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01258 | hp2 | a0001 | c0001 | t0023 | g0075 | AMR | CLM | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01361 | hp2 | a0001 | c0001 | t0029 | g0166 | AMR | CLM | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | ACB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | ACB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0229 | AFR | ACB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02027 | hp1 | a0001 | c0001 | t0038 | g0181 | EAS | KHV | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02055 | hp1 | a0001 | c0002 | t0004 | g0007 | AFR | ACB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02055 | hp2 | a0001 | c0001 | t0016 | g0214 | AFR | ACB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02074 | hp1 | a0001 | c0001 | t0043 | g0143 | EAS | KHV | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | KHV | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02132 | hp1 | a0001 | c0001 | t0011 | g0245 | EAS | KHV | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02165 | hp1 | a0001 | c0001 | t0011 | g0246 | EAS | CDX | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | CDX | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02258 | hp1 | a0001 | c0003 | t0005 | g0256 | AFR | ACB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02258 | hp2 | a0001 | c0001 | t0012 | g0014 | AFR | ACB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02280 | hp1 | a0001 | c0003 | t0005 | g0257 | AFR | ACB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02280 | hp2 | a0001 | c0002 | t0034 | g0211 | AFR | ACB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02602 | hp1 | a0001 | c0002 | t0004 | g0013 | SAS | PJL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02615 | hp2 | a0001 | c0001 | t0014 | g0022 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02630 | hp1 | a0001 | c0001 | t0014 | g0020 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02698 | hp2 | a0001 | c0002 | t0004 | g0011 | SAS | PJL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02723 | hp1 | a0001 | c0001 | t0013 | g0018 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02723 | hp2 | a0001 | c0001 | t0024 | g0098 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02738 | hp2 | a0001 | c0001 | t0015 | g0225 | SAS | PJL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02809 | hp1 | a0001 | c0001 | t0014 | g0021 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02809 | hp2 | a0001 | c0001 | t0028 | g0227 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02818 | hp1 | a0001 | c0001 | t0016 | g0212 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02886 | hp2 | a0001 | c0001 | t0046 | g0209 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0219 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0251 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0250 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02922 | hp1 | a0001 | c0001 | t0017 | g0207 | AFR | ESN | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02922 | hp2 | a0001 | c0001 | t0027 | g0226 | AFR | ESN | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02965 | hp1 | a0001 | c0002 | t0004 | g0003 | AFR | ESN | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02965 | hp2 | a0001 | c0001 | t0012 | g0015 | AFR | ESN | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02970 | hp1 | a0001 | c0001 | t0018 | g0221 | AFR | ESN | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03041 | hp2 | a0001 | c0002 | t0009 | g0204 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03130 | hp1 | a0001 | c0001 | t0019 | g0113 | AFR | ESN | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03130 | hp2 | a0001 | c0002 | t0004 | g0005 | AFR | ESN | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03139 | hp2 | a0001 | c0002 | t0004 | g0006 | AFR | ESN | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03195 | hp1 | a0001 | c0001 | t0017 | g0208 | AFR | ESN | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03195 | hp2 | a0001 | c0001 | t0025 | g0253 | AFR | ESN | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03209 | hp1 | a0001 | c0001 | t0012 | g0016 | AFR | MSL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03209 | hp2 | a0001 | c0004 | t0031 | g0222 | AFR | MSL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | MSL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0093 | AFR | MSL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0239 | SAS | PJL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03453 | hp1 | a0001 | c0001 | t0019 | g0114 | AFR | MSL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03453 | hp2 | a0001 | c0001 | t0049 | g0001 | AFR | MSL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03486 | hp2 | a0001 | c0001 | t0035 | g0017 | AFR | MSL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0198 | AFR | ESN | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0242 | AFR | GWD | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03704 | hp1 | a0001 | c0002 | t0004 | g0009 | SAS | PJL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | BEB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0051 | SAS | BEB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG04184 | hp1 | a0001 | c0002 | t0004 | g0012 | SAS | BEB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG04184 | hp2 | a0001 | c0001 | t0009 | g0162 | SAS | BEB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | STU | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0240 | AFR | YRI | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18522 | hp2 | a0001 | c0001 | t0041 | g0099 | AFR | YRI | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18939 | hp2 | a0001 | c0001 | t0006 | g0047 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18943 | hp2 | a0001 | c0001 | t0032 | g0210 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18944 | hp1 | a0001 | c0001 | t0042 | g0148 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18945 | hp1 | a0001 | c0001 | t0036 | g0046 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18946 | hp1 | a0001 | c0001 | t0007 | g0064 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18952 | hp2 | a0001 | c0001 | t0021 | g0028 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18968 | hp2 | a0001 | c0001 | t0039 | g0164 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18981 | hp1 | a0001 | c0001 | t0006 | g0048 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18981 | hp2 | a0001 | c0001 | t0020 | g0126 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18992 | hp1 | a0001 | c0001 | t0010 | g0123 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18998 | hp2 | a0001 | c0001 | t0013 | g0188 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA18999 | hp2 | a0001 | c0001 | t0011 | g0247 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19000 | hp1 | a0001 | c0001 | t0022 | g0135 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0043 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19002 | hp2 | a0001 | c0001 | t0009 | g0146 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19004 | hp2 | a0001 | c0001 | t0007 | g0083 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19009 | hp1 | a0001 | c0001 | t0024 | g0174 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19010 | hp2 | a0001 | c0001 | t0011 | g0248 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19011 | hp1 | a0001 | c0001 | t0045 | g0038 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19011 | hp2 | a0001 | c0001 | t0009 | g0155 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19030 | hp1 | a0001 | c0001 | t0025 | g0254 | AFR | LWK | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19030 | hp2 | a0001 | c0001 | t0016 | g0213 | AFR | LWK | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19043 | hp1 | a0001 | c0001 | t0020 | g0196 | AFR | LWK | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0230 | AFR | LWK | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19057 | hp2 | a0001 | c0001 | t0047 | g0150 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19058 | hp1 | a0001 | c0001 | t0006 | g0044 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19065 | hp2 | a0001 | c0001 | t0007 | g0034 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19078 | hp1 | a0001 | c0001 | t0006 | g0082 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | YRI | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0197 | AFR | YRI | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0199 | AFR | ASW | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA20129 | hp2 | a0001 | c0002 | t0004 | g0004 | AFR | ASW | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | TSI | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0193 | EUR | TSI | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | GIH | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA20905 | hp2 | a0001 | c0002 | t0048 | g0008 | SAS | GIH | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02109 | hp1 | a0001 | c0002 | t0013 | g0206 | AFR | ACB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | ACB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0255 | AFR | ACB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0104 | AFR | ACB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0220 | AFR | ACB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03471 | hp1 | a0001 | c0002 | t0004 | g0002 | AFR | MSL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG03471 | hp2 | a0001 | c0001 | t0008 | g0218 | AFR | MSL | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG06807 | hp1 | a0001 | c0001 | t0050 | g0001 | AFR | USA | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0216 | AFR | USA | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA20300 | hp1 | a0001 | c0001 | t0037 | g0019 | AFR | USA | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | USA | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | LWK | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| NA21309 | hp2 | a0001 | c0001 | t0033 | g0195 | AFR | LWK | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0004 | g0010 | REF | REF | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0238 | REF | REF | AGPS_chr2_177387773_177548834 | AGPS | chr2 | 177387773 | 177548834 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:177392996
|
A | G | 1 | a0001c0002 | 15 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(12): Show |
synonymous_variant | LOW | c.207A>G | p.Ala69Ala | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/20 | 224/7633 | 207/1977 | 69/658 | chr2 | 177392996 | ||
| chr2:177482126
|
C | G | 1 | a0001c0003 | 3 | HG02258.hp1 HG02280.hp1 HG02486.hp1 |
synonymous_variant | LOW | c.1173C>G | p.Gly391Gly | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/20 | 1190/7633 | 1173/1977 | 391/658 | chr2 | 177482126 | ||
| chr2:177521275
|
G | A | 1 | a0001c0004 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1704G>A | p.Thr568Thr | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 18/20 | 1721/7633 | 1704/1977 | 568/658 | chr2 | 177521275 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:177538313
|
A | G | 1 | a0001c0001t0051 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*118A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 118 | chr2 | 177538313 | |||||
| chr2:177538361
|
G | A | 1 | a0001c0001t0026 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*166G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 166 | chr2 | 177538361 | |||||
| chr2:177538572
|
C | G | 3 | a0001c0001t0016a0001c0001t0049a0001c0001t0050 | 5 | HG02055.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*377C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 377 | chr2 | 177538572 | |||||
| chr2:177538612
|
G | A | 2 | a0001c0001t0027a0001c0001t0028 | 2 | HG02809.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*417G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 417 | chr2 | 177538612 | |||||
| chr2:177538709
|
T | G | 1 | a0001c0001t0017 | 2 | HG02922.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*514T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 514 | chr2 | 177538709 | |||||
| chr2:177538747
|
T | G | 3 | a0001c0001t0016a0001c0001t0049a0001c0001t0050 | 5 | HG02055.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*552T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 552 | chr2 | 177538747 | |||||
| chr2:177538916
|
T | C | 1 | a0001c0001t0027 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*721T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 721 | chr2 | 177538916 | |||||
| chr2:177539060
|
A | G | 1 | a0001c0001t0007 | 6 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*865A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 865 | chr2 | 177539060 | |||||
| chr2:177539300
|
T | A | 1 | a0001c0001t0029 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1105T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1105 | chr2 | 177539300 | |||||
| chr2:177539301
|
A | T | 3 | a0001c0001t0004a0001c0002t0004a0001c0002t0048 | 13 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1106A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1106 | chr2 | 177539301 | |||||
| chr2:177539348
|
C | T | 1 | a0001c0001t0047 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1153C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1153 | chr2 | 177539348 | |||||
| chr2:177539503
|
C | T | 1 | a0001c0001t0046 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1308C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1308 | chr2 | 177539503 | |||||
| chr2:177539559
|
A | G | 2 | a0001c0001t0017a0001c0001t0046 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1364A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1364 | chr2 | 177539559 | |||||
| chr2:177539668
|
A | C | 1 | a0001c0001t0045 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1473A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1473 | chr2 | 177539668 | |||||
| chr2:177539756
|
G | T | 1 | a0001c0001t0050 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1561G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1561 | chr2 | 177539756 | |||||
| chr2:177539896
|
T | C | 1 | a0001c0001t0030 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1701T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1701 | chr2 | 177539896 | |||||
| chr2:177539907
|
TTGA | T | 2 | a0001c0001t0008a0001c0001t0018 | 7 | HG01109.hp1 HG01243.hp1 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1716_*1718delTGA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1716 | INFO_REALIGN_3_PRIME | chr2 | 177539907 | ||||
| chr2:177539914
|
G | A | 1 | a0001c0004t0031 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1719G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1719 | chr2 | 177539914 | |||||
| chr2:177540007
|
T | TAAAG | 47 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(44): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*1814_*1815insAGAA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1815 | INFO_REALIGN_3_PRIME | chr2 | 177540007 | ||||
| chr2:177540031
|
G | GTA | 5 | a0001c0001t0011a0001c0001t0018a0001c0001t0032others(2): Show | 9 | HG01109.hp1 HG02132.hp1 HG02165.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1858_*1859dupAT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1860 | INFO_REALIGN_3_PRIME | chr2 | 177540031 | ||||
| chr2:177540031
|
GTA | G | 2 | a0001c0001t0014a0001c0001t0044 | 4 | HG01167.hp1 HG02615.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1858_*1859delAT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1858 | INFO_REALIGN_3_PRIME | chr2 | 177540031 | ||||
| chr2:177540031
|
GTATATA | G | 4 | a0001c0001t0004a0001c0001t0025a0001c0002t0004others(1): Show | 15 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1854_*1859delATAT others(2): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1854 | INFO_REALIGN_3_PRIME | chr2 | 177540031 | ||||
| chr2:177540031
|
GTATATAT others(45): Show |
G | 1 | a0001c0001t0045 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1848_*1899delATAT others(48): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1848 | INFO_REALIGN_3_PRIME | chr2 | 177540031 | ||||
| chr2:177540053
|
ATG | A | 5 | a0001c0001t0009a0001c0001t0020a0001c0001t0036others(2): Show | 9 | HG01109.hp2 HG02280.hp2 HG03041.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1860_*1861delGT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1860 | INFO_REALIGN_3_PRIME | chr2 | 177540053 | ||||
| chr2:177540055
|
G | A | 10 | a0001c0001t0005a0001c0001t0011a0001c0001t0012others(7): Show | 25 | HG00735.hp1 HG01891.hp1 HG02109.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1860G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1860 | chr2 | 177540055 | |||||
| chr2:177540057
|
A | ATATG | 1 | a0001c0001t0012 | 3 | HG02258.hp2 HG02965.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1863_*1864insATGT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1864 | INFO_REALIGN_3_PRIME | chr2 | 177540057 | ||||
| chr2:177540057
|
A | G | 1 | a0001c0001t0037 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1862A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1862 | chr2 | 177540057 | |||||
| chr2:177540060
|
C | T | 15 | a0001c0001t0005a0001c0001t0009a0001c0001t0011others(12): Show | 34 | HG00735.hp1 HG01109.hp2 HG01891.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1865C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1865 | chr2 | 177540060 | |||||
| chr2:177540060
|
CAT | C | 7 | a0001c0001t0004a0001c0001t0021a0001c0001t0022others(4): Show | 20 | HG00438.hp1 HG00673.hp2 HG02055.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1866_*1867delAT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1866 | chr2 | 177540060 | |||||
| chr2:177540061
|
A | G | 26 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(23): Show | 181 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*1866A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1866 | chr2 | 177540061 | |||||
| chr2:177540062
|
T | TGC | 2 | a0001c0001t0019a0001c0001t0033 | 3 | HG03130.hp1 HG03453.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1868_*1869insCG | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1869 | INFO_REALIGN_3_PRIME | chr2 | 177540062 | ||||
| chr2:177540064
|
T | C | 13 | a0001c0001t0005a0001c0001t0009a0001c0001t0011others(10): Show | 31 | HG00735.hp1 HG01109.hp2 HG01891.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1869T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1869 | chr2 | 177540064 | |||||
| chr2:177540073
|
GTA | G | 2 | a0001c0001t0015a0001c0001t0051 | 4 | HG01167.hp2 HG01169.hp1 HG01175.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1898_*1899delAT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1898 | INFO_REALIGN_3_PRIME | chr2 | 177540073 | ||||
| chr2:177540073
|
GTATA | G | 20 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(17): Show | 165 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*1896_*1899delATAT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1896 | INFO_REALIGN_3_PRIME | chr2 | 177540073 | ||||
| chr2:177540073
|
GTATATA | G | 6 | a0001c0001t0008a0001c0001t0010a0001c0001t0016others(3): Show | 16 | HG00544.hp2 HG00597.hp1 HG01109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1894_*1899delATAT others(2): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1894 | INFO_REALIGN_3_PRIME | chr2 | 177540073 | ||||
| chr2:177540075
|
A | G | 21 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(18): Show | 53 | HG00438.hp1 HG00673.hp2 HG00735.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1880A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1880 | chr2 | 177540075 | |||||
| chr2:177540077
|
A | G | 17 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(14): Show | 47 | HG00735.hp1 HG01109.hp2 HG01891.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1882A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1882 | chr2 | 177540077 | |||||
| chr2:177540079
|
A | G | 2 | a0001c0001t0014a0001c0001t0024 | 5 | HG02615.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1884A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 1884 | chr2 | 177540079 | |||||
| chr2:177540286
|
T | C | 2 | a0001c0001t0011a0001c0001t0038 | 5 | HG02027.hp1 HG02132.hp1 HG02165.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2091T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 2091 | chr2 | 177540286 | |||||
| chr2:177540513
|
A | G | 2 | a0001c0001t0017a0001c0001t0046 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2318A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 2318 | chr2 | 177540513 | |||||
| chr2:177540743
|
A | G | 2 | a0001c0001t0006a0001c0001t0036 | 8 | HG00544.hp1 HG00597.hp2 NA18939.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2548A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 2548 | chr2 | 177540743 | |||||
| chr2:177540831
|
G | C | 4 | a0001c0001t0004a0001c0001t0025a0001c0002t0004others(1): Show | 15 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2636G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 2636 | chr2 | 177540831 | |||||
| chr2:177541240
|
C | T | 1 | a0001c0001t0043 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3045C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 3045 | chr2 | 177541240 | |||||
| chr2:177541301
|
T | G | 1 | a0001c0001t0039 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3106T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 3106 | chr2 | 177541301 | |||||
| chr2:177541753
|
C | T | 28 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(25): Show | 135 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*3558C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 3558 | chr2 | 177541753 | |||||
| chr2:177542041
|
A | AT | 48 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(45): Show | 234 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*3854dupT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 3855 | INFO_REALIGN_3_PRIME | chr2 | 177542041 | ||||
| chr2:177542074
|
T | C | 1 | a0001c0001t0049 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3879T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 3879 | chr2 | 177542074 | |||||
| chr2:177542089
|
A | G | 1 | a0001c0004t0031 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3894A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 3894 | chr2 | 177542089 | |||||
| chr2:177542101
|
CTTTTAG | C | 2 | a0001c0001t0015a0001c0001t0051 | 4 | HG01167.hp2 HG01169.hp1 HG01175.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3917_*3922delAGTT others(2): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 3917 | INFO_REALIGN_3_PRIME | chr2 | 177542101 | ||||
| chr2:177542126
|
A | G | 1 | a0001c0001t0040 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3931A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 3931 | chr2 | 177542126 | |||||
| chr2:177542166
|
A | G | 2 | a0001c0001t0017a0001c0001t0046 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3971A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 3971 | chr2 | 177542166 | |||||
| chr2:177542293
|
C | T | 2 | a0001c0001t0033a0001c0001t0035 | 2 | HG03486.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4098C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 4098 | chr2 | 177542293 | |||||
| chr2:177542448
|
C | A | 45 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(42): Show | 228 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*4253C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 4253 | chr2 | 177542448 | |||||
| chr2:177542450
|
T | G | 1 | a0001c0001t0014 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4255T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 4255 | chr2 | 177542450 | |||||
| chr2:177542710
|
CAT | C | 16 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(13): Show | 90 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*4516_*4517delAT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 4516 | chr2 | 177542710 | |||||
| chr2:177542813
|
A | G | 4 | a0001c0001t0004a0001c0001t0025a0001c0002t0004others(1): Show | 15 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4618A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 4618 | chr2 | 177542813 | |||||
| chr2:177542845
|
AT | A | 5 | a0001c0001t0008a0001c0001t0016a0001c0001t0018others(2): Show | 12 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4660delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 4660 | INFO_REALIGN_3_PRIME | chr2 | 177542845 | ||||
| chr2:177543016
|
C | T | 2 | a0001c0001t0005a0001c0003t0005 | 10 | HG00735.hp1 HG01891.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4821C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 4821 | chr2 | 177543016 | |||||
| chr2:177543143
|
T | G | 1 | a0001c0002t0048 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4948T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 4948 | chr2 | 177543143 | |||||
| chr2:177543169
|
T | C | 45 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(42): Show | 228 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*4974T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 4974 | chr2 | 177543169 | |||||
| chr2:177543221
|
C | T | 1 | a0001c0001t0042 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5026C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5026 | chr2 | 177543221 | |||||
| chr2:177543291
|
T | C | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5096T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5096 | chr2 | 177543291 | |||||
| chr2:177543292
|
T | A | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5097T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5097 | chr2 | 177543292 | |||||
| chr2:177543293
|
T | A | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5098T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5098 | chr2 | 177543293 | |||||
| chr2:177543294
|
T | A | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5099T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5099 | chr2 | 177543294 | |||||
| chr2:177543295
|
C | G | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5100C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5100 | chr2 | 177543295 | |||||
| chr2:177543296
|
G | T | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5101G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5101 | chr2 | 177543296 | |||||
| chr2:177543302
|
T | G | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5107T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5107 | chr2 | 177543302 | |||||
| chr2:177543303
|
G | A | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5108G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5108 | chr2 | 177543303 | |||||
| chr2:177543304
|
G | GGAATTAA others(3): Show |
1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5109_*5110insGAAT others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5110 | chr2 | 177543304 | |||||
| chr2:177543305
|
T | C | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5110T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5110 | chr2 | 177543305 | |||||
| chr2:177543306
|
G | A | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5111G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5111 | chr2 | 177543306 | |||||
| chr2:177543307
|
C | A | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5112C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5112 | chr2 | 177543307 | |||||
| chr2:177543316
|
T | G | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5121T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5121 | chr2 | 177543316 | |||||
| chr2:177543317
|
A | G | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5122A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5122 | chr2 | 177543317 | |||||
| chr2:177543318
|
A | T | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5123A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5123 | chr2 | 177543318 | |||||
| chr2:177543319
|
C | A | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5124C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5124 | chr2 | 177543319 | |||||
| chr2:177543319
|
C | T | 1 | a0001c0001t0014 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5124C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5124 | chr2 | 177543319 | |||||
| chr2:177543324
|
A | T | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5129A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5129 | chr2 | 177543324 | |||||
| chr2:177543326
|
T | A | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5131T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5131 | chr2 | 177543326 | |||||
| chr2:177543327
|
T | A | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5132T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5132 | chr2 | 177543327 | |||||
| chr2:177543328
|
C | G | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5133C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5133 | chr2 | 177543328 | |||||
| chr2:177543330
|
G | A | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5135G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5135 | chr2 | 177543330 | |||||
| chr2:177543333
|
C | T | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5138C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5138 | chr2 | 177543333 | |||||
| chr2:177543338
|
C | A | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5143C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5143 | chr2 | 177543338 | |||||
| chr2:177543342
|
G | C | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5147G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5147 | chr2 | 177543342 | |||||
| chr2:177543344
|
T | A | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5149T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5149 | chr2 | 177543344 | |||||
| chr2:177543346
|
A | C | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5151A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5151 | chr2 | 177543346 | |||||
| chr2:177543348
|
A | T | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5153A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5153 | chr2 | 177543348 | |||||
| chr2:177543352
|
T | C | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5157T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5157 | chr2 | 177543352 | |||||
| chr2:177543362
|
A | C | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5167A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5167 | chr2 | 177543362 | |||||
| chr2:177543363
|
T | C | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5168T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5168 | chr2 | 177543363 | |||||
| chr2:177543367
|
T | G | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5172T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5172 | chr2 | 177543367 | |||||
| chr2:177543368
|
A | T | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5173A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5173 | chr2 | 177543368 | |||||
| chr2:177543369
|
G | C | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5174G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5174 | chr2 | 177543369 | |||||
| chr2:177543370
|
G | C | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5175G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5175 | chr2 | 177543370 | |||||
| chr2:177543372
|
T | G | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5177T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5177 | chr2 | 177543372 | |||||
| chr2:177543376
|
T | C | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5181T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5181 | chr2 | 177543376 | |||||
| chr2:177543382
|
C | A | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5187C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 20/20 | 5187 | chr2 | 177543382 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:177393111
|
A | C | 5 | a0001c0001t0025g0253a0001c0001t0025g0254a0001c0003t0001g0255others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.260+62A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177393111 | ||||||
| chr2:177393373
|
T | C | 17 | a0001c0001t0025g0253a0001c0001t0025g0254a0001c0002t0004g0002others(14): Show | 17 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.260+324T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177393373 | ||||||
| chr2:177393431
|
A | C | 1 | a0001c0001t0001g0252 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.260+382A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177393431 | ||||||
| chr2:177393452
|
C | A | 3 | a0001c0001t0012g0014a0001c0001t0012g0015a0001c0001t0012g0016 | 3 | HG02258.hp2 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.260+403C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177393452 | ||||||
| chr2:177393471
|
C | G | 2 | a0001c0001t0005g0250a0001c0001t0005g0251 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.260+422C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177393471 | ||||||
| chr2:177393679
|
A | G | 1 | a0001c0001t0002g0249 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.260+630A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177393679 | ||||||
| chr2:177393720
|
T | C | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.260+671T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177393720 | ||||||
| chr2:177393746
|
ATCT | A | 12 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.260+699_260+701del others(3): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177393746 | |||||
| chr2:177393748
|
C | CT | 27 | a0001c0001t0001g0203a0001c0001t0002g0202a0001c0001t0010g0205others(24): Show | 27 | HG00544.hp2 HG02055.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.260+714dupT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177393748 | |||||
| chr2:177394001
|
C | T | 7 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(4): Show | 7 | HG00735.hp1 HG01891.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.260+952C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177394001 | ||||||
| chr2:177394028
|
G | A | 1 | a0001c0001t0035g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.260+979G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177394028 | ||||||
| chr2:177394061
|
C | CA | 5 | a0001c0001t0016g0212a0001c0001t0016g0213a0001c0001t0016g0214others(2): Show | 5 | HG02055.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.260+1013dupA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177394061 | |||||
| chr2:177394122
|
C | T | 1 | a0001c0001t0018g0221 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.260+1073C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177394122 | ||||||
| chr2:177394200
|
G | A | 5 | a0001c0001t0012g0014a0001c0001t0012g0015a0001c0001t0012g0016others(2): Show | 5 | HG02258.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.260+1151G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177394200 | ||||||
| chr2:177394251
|
C | A | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.260+1202C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177394251 | ||||||
| chr2:177394330
|
T | C | 1 | a0001c0001t0013g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.260+1281T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177394330 | ||||||
| chr2:177394372
|
C | T | 1 | a0001c0001t0011g0248 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.260+1323C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177394372 | ||||||
| chr2:177394487
|
A | G | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+1438A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177394487 | ||||||
| chr2:177394501
|
AG | A | 70 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(67): Show | 70 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.260+1456delG | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177394501 | |||||
| chr2:177394546
|
G | A | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.260+1497G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177394546 | ||||||
| chr2:177394600
|
T | A | 1 | a0001c0001t0009g0091 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.260+1551T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177394600 | ||||||
| chr2:177394629
|
A | G | 1 | a0001c0001t0013g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.260+1580A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177394629 | ||||||
| chr2:177394671
|
C | T | 2 | a0001c0001t0013g0018a0001c0001t0037g0019 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.260+1622C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177394671 | ||||||
| chr2:177394677
|
A | G | 5 | a0001c0001t0016g0212a0001c0001t0016g0213a0001c0001t0016g0214others(2): Show | 5 | HG02055.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.260+1628A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177394677 | ||||||
| chr2:177394822
|
C | T | 73 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.260+1773C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177394822 | ||||||
| chr2:177394838
|
T | C | 17 | a0001c0001t0025g0253a0001c0001t0025g0254a0001c0002t0004g0002others(14): Show | 17 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.260+1789T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177394838 | ||||||
| chr2:177394950
|
G | A | 17 | a0001c0001t0025g0253a0001c0001t0025g0254a0001c0002t0004g0002others(14): Show | 17 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.260+1901G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177394950 | ||||||
| chr2:177394988
|
A | G | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG01256.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.260+1939A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177394988 | ||||||
| chr2:177394988
|
A | T | 1 | a0001c0001t0002g0090 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.260+1939A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177394988 | ||||||
| chr2:177395014
|
G | C | 2 | a0001c0001t0033g0195a0001c0001t0035g0017 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.260+1965G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177395014 | ||||||
| chr2:177395746
|
A | G | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.260+2697A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177395746 | ||||||
| chr2:177395971
|
T | C | 14 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(11): Show | 14 | HG01361.hp1 HG01884.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.260+2922T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177395971 | ||||||
| chr2:177396238
|
G | A | 7 | a0001c0001t0001g0092a0001c0001t0001g0105a0001c0001t0001g0106others(4): Show | 7 | HG00642.hp1 HG01257.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.260+3189G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177396238 | ||||||
| chr2:177396308
|
T | C | 7 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(4): Show | 7 | HG01109.hp1 HG01243.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.260+3259T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177396308 | ||||||
| chr2:177396328
|
C | T | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+3279C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177396328 | ||||||
| chr2:177396376
|
A | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.260+3327A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177396376 | ||||||
| chr2:177396537
|
T | C | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+3488T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177396537 | ||||||
| chr2:177396580
|
T | C | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+3531T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177396580 | ||||||
| chr2:177396653
|
C | T | 2 | a0001c0002t0004g0012a0001c0002t0004g0013 | 2 | HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.260+3604C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177396653 | ||||||
| chr2:177396927
|
A | G | 3 | a0001c0001t0012g0014a0001c0001t0012g0015a0001c0001t0012g0016 | 3 | HG02258.hp2 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.260+3878A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177396927 | ||||||
| chr2:177396937
|
C | CTTTTCTT | 155 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(152): Show | 155 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.260+3893_260+3899d others(9): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177396937 | |||||
| chr2:177396942
|
C | CTTTTTTC others(1): Show |
73 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0002g0023others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.260+3899_260+3900i others(10): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177396942 | |||||
| chr2:177396942
|
C | CTTTTTTT others(23): Show |
1 | a0001c0001t0011g0245 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.260+3907_260+3908i others(32): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177396942 | |||||
| chr2:177396942
|
C | CTTTTTTT others(29): Show |
2 | a0001c0001t0011g0246a0001c0001t0011g0248 | 2 | HG02165.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.260+3907_260+3908i others(38): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177396942 | |||||
| chr2:177396942
|
C | CTTTTTTT others(30): Show |
1 | a0001c0001t0011g0247 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.260+3907_260+3908i others(39): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177396942 | |||||
| chr2:177397040
|
A | G | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0013g0188others(1): Show | 4 | NA18939.hp1 NA18943.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.260+3991A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177397040 | ||||||
| chr2:177397064
|
G | A | 17 | a0001c0001t0025g0253a0001c0001t0025g0254a0001c0002t0004g0002others(14): Show | 17 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.260+4015G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177397064 | ||||||
| chr2:177397100
|
A | G | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.260+4051A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177397100 | ||||||
| chr2:177397317
|
C | T | 1 | a0001c0002t0004g0013 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.260+4268C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177397317 | ||||||
| chr2:177397391
|
A | AT | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.260+4346dupT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177397391 | |||||
| chr2:177397469
|
GT | G | 6 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0002g0023others(3): Show | 6 | HG02818.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.260+4434delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177397469 | |||||
| chr2:177397649
|
C | T | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+4600C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177397649 | ||||||
| chr2:177397673
|
G | T | 73 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.260+4624G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177397673 | ||||||
| chr2:177397746
|
C | T | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+4697C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177397746 | ||||||
| chr2:177397752
|
G | A | 6 | a0001c0001t0015g0223a0001c0001t0015g0224a0001c0001t0015g0225others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.260+4703G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177397752 | ||||||
| chr2:177397772
|
T | C | 2 | a0001c0001t0018g0215a0001c0001t0018g0221 | 2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.260+4723T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177397772 | ||||||
| chr2:177398027
|
G | A | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.260+4978G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177398027 | ||||||
| chr2:177398216
|
A | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.260+5167A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177398216 | ||||||
| chr2:177398368
|
G | A | 1 | a0001c0001t0005g0197 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.260+5319G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177398368 | ||||||
| chr2:177398484
|
T | A | 1 | a0001c0001t0003g0229 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.260+5435T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177398484 | ||||||
| chr2:177398567
|
G | C | 12 | a0001c0002t0004g0002a0001c0002t0004g0003a0001c0002t0004g0004others(9): Show | 12 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.260+5518G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177398567 | ||||||
| chr2:177398576
|
G | A | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+5527G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177398576 | ||||||
| chr2:177398680
|
TAAG | T | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+5635_260+5637d others(5): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177398680 | |||||
| chr2:177399181
|
T | C | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+6132T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177399181 | ||||||
| chr2:177399267
|
C | T | 1 | a0001c0001t0002g0087 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.260+6218C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177399267 | ||||||
| chr2:177399671
|
C | T | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.260+6622C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177399671 | ||||||
| chr2:177399776
|
C | T | 3 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG00423.hp1 NA18980.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.260+6727C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177399776 | ||||||
| chr2:177399845
|
T | C | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+6796T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177399845 | ||||||
| chr2:177399917
|
A | G | 3 | a0001c0003t0001g0255a0001c0003t0005g0256a0001c0003t0005g0257 | 3 | HG02258.hp1 HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.260+6868A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177399917 | ||||||
| chr2:177400033
|
G | A | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.260+6984G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177400033 | ||||||
| chr2:177400689
|
C | T | 1 | a0001c0001t0030g0244 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.260+7640C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177400689 | ||||||
| chr2:177401565
|
G | A | 1 | a0001c0001t0013g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.260+8516G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177401565 | ||||||
| chr2:177401575
|
C | T | 3 | a0001c0001t0012g0014a0001c0001t0012g0015a0001c0001t0012g0016 | 3 | HG02258.hp2 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.260+8526C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177401575 | ||||||
| chr2:177401792
|
C | T | 2 | a0001c0001t0033g0195a0001c0001t0035g0017 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.260+8743C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177401792 | ||||||
| chr2:177402110
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.260+9061T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177402110 | ||||||
| chr2:177402167
|
T | C | 1 | a0001c0001t0003g0229 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.260+9118T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177402167 | ||||||
| chr2:177402311
|
A | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.260+9262A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177402311 | ||||||
| chr2:177402582
|
G | C | 96 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(93): Show | 96 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.260+9533G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177402582 | ||||||
| chr2:177402685
|
A | G | 2 | a0001c0001t0049g0001a0001c0001t0050g0001 | 2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.260+9636A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177402685 | ||||||
| chr2:177402767
|
C | A | 1 | a0001c0001t0001g0115 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.260+9718C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177402767 | ||||||
| chr2:177402774
|
T | C | 233 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(230): Show | 233 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.260+9725T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177402774 | ||||||
| chr2:177402795
|
G | A | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.260+9746G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177402795 | ||||||
| chr2:177403005
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.260+9956C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177403005 | ||||||
| chr2:177403008
|
G | A | 13 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(10): Show | 13 | HG01361.hp1 HG01884.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.260+9959G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177403008 | ||||||
| chr2:177403015
|
C | T | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+9966C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177403015 | ||||||
| chr2:177403117
|
T | A | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.260+10068T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177403117 | ||||||
| chr2:177403251
|
A | G | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+10202A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177403251 | ||||||
| chr2:177403313
|
A | T | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.260+10264A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177403313 | ||||||
| chr2:177403436
|
A | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.260+10387A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177403436 | ||||||
| chr2:177403551
|
A | G | 73 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.260+10502A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177403551 | ||||||
| chr2:177403774
|
T | C | 1 | a0001c0001t0033g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.260+10725T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177403774 | ||||||
| chr2:177403924
|
C | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.260+10875C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177403924 | ||||||
| chr2:177403960
|
T | G | 1 | a0001c0002t0004g0002 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.260+10911T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177403960 | ||||||
| chr2:177404096
|
A | C | 2 | a0001c0001t0005g0250a0001c0001t0005g0251 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.260+11047A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177404096 | ||||||
| chr2:177404314
|
C | T | 5 | a0001c0001t0016g0212a0001c0001t0016g0213a0001c0001t0016g0214others(2): Show | 5 | HG02055.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.260+11265C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177404314 | ||||||
| chr2:177404565
|
A | G | 1 | a0001c0001t0007g0083 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.260+11516A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177404565 | ||||||
| chr2:177404621
|
A | T | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+11572A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177404621 | ||||||
| chr2:177404803
|
A | T | 134 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(131): Show | 134 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.260+11754A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177404803 | ||||||
| chr2:177404921
|
G | C | 1 | a0001c0001t0033g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.260+11872G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177404921 | ||||||
| chr2:177404996
|
T | G | 12 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.260+11947T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177404996 | ||||||
| chr2:177405108
|
T | G | 1 | a0001c0001t0002g0090 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.260+12059T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177405108 | ||||||
| chr2:177405188
|
C | G | 1 | a0001c0001t0001g0105 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.260+12139C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177405188 | ||||||
| chr2:177405282
|
C | A | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0013g0188others(1): Show | 4 | NA18939.hp1 NA18943.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.260+12233C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177405282 | ||||||
| chr2:177405521
|
G | A | 1 | a0001c0002t0004g0002 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.260+12472G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177405521 | ||||||
| chr2:177405606
|
A | C | 2 | a0001c0002t0004g0010a0001c0002t0004g0011 | 2 | HG02698.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.260+12557A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177405606 | ||||||
| chr2:177405660
|
G | A | 2 | a0001c0001t0005g0250a0001c0001t0005g0251 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.260+12611G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177405660 | ||||||
| chr2:177405667
|
T | C | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.260+12618T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177405667 | ||||||
| chr2:177405673
|
G | GT | 187 | a0001c0001t0001g0094a0001c0001t0001g0105a0001c0001t0001g0106others(184): Show | 187 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.260+12639dupT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177405673 | |||||
| chr2:177405673
|
G | GTT | 36 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0096others(33): Show | 36 | HG00735.hp1 HG01361.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.260+12638_260+1263 others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177405673 | |||||
| chr2:177405673
|
G | GTTT | 6 | a0001c0001t0005g0104a0001c0001t0012g0014a0001c0001t0012g0015others(3): Show | 6 | HG02258.hp2 HG02486.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.260+12637_260+1263 others(7): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177405673 | |||||
| chr2:177405676
|
T | G | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+12627T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177405676 | ||||||
| chr2:177405772
|
C | G | 2 | a0001c0001t0008g0219a0001c0001t0008g0220 | 2 | HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.260+12723C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177405772 | ||||||
| chr2:177405837
|
T | G | 1 | a0001c0001t0001g0117 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.260+12788T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177405837 | ||||||
| chr2:177405846
|
C | CT | 236 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(233): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.260+12800dupT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177405846 | |||||
| chr2:177405863
|
TAACTCTC | T | 3 | a0001c0001t0011g0246a0001c0001t0011g0247a0001c0001t0011g0248 | 3 | HG02165.hp1 NA18999.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.260+12823_260+1282 others(11): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177405863 | |||||
| chr2:177406006
|
G | A | 70 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(67): Show | 70 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.260+12957G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177406006 | ||||||
| chr2:177406131
|
C | CGACTCTC others(4): Show |
1 | a0001c0001t0002g0080 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.260+13083_260+1309 others(15): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177406131 | |||||
| chr2:177406131
|
C | T | 6 | a0001c0002t0004g0009a0001c0002t0004g0010a0001c0002t0004g0011others(3): Show | 6 | HG02602.hp1 HG02698.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.260+13082C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177406131 | ||||||
| chr2:177406502
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.260+13453G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177406502 | ||||||
| chr2:177406544
|
A | G | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+13495A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177406544 | ||||||
| chr2:177406965
|
C | A | 3 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121 | 3 | NA19058.hp2 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.261-13304C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177406965 | ||||||
| chr2:177407125
|
T | C | 71 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(68): Show | 71 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.261-13144T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177407125 | ||||||
| chr2:177407185
|
G | T | 1 | a0001c0001t0003g0243 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.261-13084G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177407185 | ||||||
| chr2:177407207
|
A | G | 2 | a0001c0001t0005g0250a0001c0001t0005g0251 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.261-13062A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177407207 | ||||||
| chr2:177407317
|
A | G | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.261-12952A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177407317 | ||||||
| chr2:177407331
|
A | G | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.261-12938A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177407331 | ||||||
| chr2:177407437
|
T | G | 8 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(5): Show | 8 | HG00408.hp1 HG00438.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.261-12832T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177407437 | ||||||
| chr2:177407662
|
C | T | 5 | a0001c0001t0016g0212a0001c0001t0016g0213a0001c0001t0016g0214others(2): Show | 5 | HG02055.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.261-12607C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177407662 | ||||||
| chr2:177407792
|
CT | C | 132 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(129): Show | 132 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.261-12460delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177407792 | |||||
| chr2:177407792
|
CTT | C | 10 | a0001c0001t0001g0115a0001c0001t0001g0119a0001c0001t0001g0124others(7): Show | 10 | HG02109.hp2 HG02258.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.261-12461_261-1246 others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177407792 | |||||
| chr2:177407809
|
T | A | 14 | a0001c0001t0001g0106a0001c0001t0001g0122a0001c0001t0002g0030others(11): Show | 14 | HG01167.hp2 HG01169.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.261-12460T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177407809 | ||||||
| chr2:177407810
|
A | T | 19 | a0001c0001t0004g0093a0001c0001t0011g0245a0001c0001t0011g0246others(16): Show | 19 | HG02055.hp1 HG02132.hp1 HG02165.hp1 others(16): Show |
intron_variant | MODIFIER | c.261-12459A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177407810 | ||||||
| chr2:177407900
|
A | G | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.261-12369A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177407900 | ||||||
| chr2:177408094
|
T | C | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.261-12175T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177408094 | ||||||
| chr2:177408364
|
T | C | 7 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(4): Show | 7 | HG00735.hp1 HG01891.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-11905T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177408364 | ||||||
| chr2:177408416
|
C | T | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.261-11853C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177408416 | ||||||
| chr2:177408529
|
G | T | 2 | a0001c0001t0002g0037a0001c0001t0002g0079 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.261-11740G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177408529 | ||||||
| chr2:177408637
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.261-11632C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177408637 | ||||||
| chr2:177408935
|
G | A | 3 | a0001c0001t0011g0246a0001c0001t0011g0247a0001c0001t0011g0248 | 3 | HG02165.hp1 NA18999.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.261-11334G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177408935 | ||||||
| chr2:177409061
|
C | T | 1 | a0001c0001t0002g0031 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.261-11208C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177409061 | ||||||
| chr2:177409155
|
GC | G | 104 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(101): Show | 104 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.261-11113delC | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177409155 | ||||||
| chr2:177409217
|
T | G | 2 | a0001c0001t0002g0089a0001c0001t0045g0038 | 2 | NA18949.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.261-11052T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177409217 | ||||||
| chr2:177409231
|
GT | G | 139 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(136): Show | 139 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.261-11029delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177409231 | |||||
| chr2:177409263
|
G | A | 12 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(9): Show | 12 | HG01884.hp2 HG02486.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.261-11006G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177409263 | ||||||
| chr2:177409388
|
CT | C | 137 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(134): Show | 137 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.261-10865delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177409388 | |||||
| chr2:177409388
|
CTT | C | 94 | a0001c0001t0001g0125a0001c0001t0002g0023a0001c0001t0002g0024others(91): Show | 94 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.261-10866_261-1086 others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177409388 | |||||
| chr2:177409404
|
T | A | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.261-10865T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177409404 | ||||||
| chr2:177409412
|
G | A | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.261-10857G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177409412 | ||||||
| chr2:177409505
|
C | T | 2 | a0001c0002t0004g0012a0001c0002t0004g0013 | 2 | HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.261-10764C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177409505 | ||||||
| chr2:177409506
|
G | A | 1 | a0001c0001t0003g0233 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.261-10763G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177409506 | ||||||
| chr2:177409579
|
G | A | 73 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.261-10690G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177409579 | ||||||
| chr2:177409629
|
G | A | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.261-10640G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177409629 | ||||||
| chr2:177409798
|
A | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.261-10471A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177409798 | ||||||
| chr2:177410136
|
C | G | 1 | a0001c0001t0016g0214 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.261-10133C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177410136 | ||||||
| chr2:177410136
|
C | T | 2 | a0001c0001t0003g0241a0001c0001t0003g0242 | 2 | HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.261-10133C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177410136 | ||||||
| chr2:177410381
|
C | T | 5 | a0001c0001t0002g0078a0001c0001t0011g0245a0001c0001t0011g0246others(2): Show | 5 | HG02132.hp1 HG02165.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.261-9888C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177410381 | ||||||
| chr2:177410500
|
T | C | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.261-9769T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177410500 | ||||||
| chr2:177410593
|
A | T | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.261-9676A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177410593 | ||||||
| chr2:177410699
|
C | T | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.261-9570C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177410699 | ||||||
| chr2:177410796
|
C | T | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.261-9473C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177410796 | ||||||
| chr2:177410797
|
G | A | 7 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(4): Show | 7 | HG00735.hp1 HG01891.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-9472G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177410797 | ||||||
| chr2:177410812
|
C | T | 1 | a0001c0001t0007g0077 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.261-9457C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177410812 | ||||||
| chr2:177410940
|
A | T | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.261-9329A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177410940 | ||||||
| chr2:177410948
|
A | G | 1 | a0001c0001t0001g0116 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.261-9321A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177410948 | ||||||
| chr2:177411070
|
C | T | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.261-9199C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177411070 | ||||||
| chr2:177411159
|
G | A | 89 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(86): Show | 89 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.261-9110G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177411159 | ||||||
| chr2:177411246
|
A | T | 1 | a0001c0001t0002g0076 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.261-9023A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177411246 | ||||||
| chr2:177411323
|
G | A | 1 | a0001c0001t0003g0234 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261-8946G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177411323 | ||||||
| chr2:177411525
|
G | C | 3 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121 | 3 | NA19058.hp2 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.261-8744G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177411525 | ||||||
| chr2:177411753
|
G | C | 1 | a0001c0001t0033g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.261-8516G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177411753 | ||||||
| chr2:177411802
|
A | G | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.261-8467A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177411802 | ||||||
| chr2:177411821
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0186 | 2 | NA18969.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.261-8448A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177411821 | ||||||
| chr2:177411844
|
A | G | 127 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(124): Show | 127 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.261-8425A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177411844 | ||||||
| chr2:177411876
|
T | C | 1 | a0001c0001t0002g0039 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.261-8393T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177411876 | ||||||
| chr2:177411988
|
G | A | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.261-8281G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177411988 | ||||||
| chr2:177412040
|
C | A | 12 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.261-8229C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177412040 | ||||||
| chr2:177412326
|
A | G | 236 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(233): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.261-7943A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177412326 | ||||||
| chr2:177412363
|
C | T | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.261-7906C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177412363 | ||||||
| chr2:177412443
|
T | A | 5 | a0001c0001t0025g0253a0001c0001t0025g0254a0001c0003t0001g0255others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.261-7826T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177412443 | ||||||
| chr2:177412523
|
C | T | 76 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(73): Show | 76 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.261-7746C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177412523 | ||||||
| chr2:177412593
|
C | T | 5 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0014g0020others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.261-7676C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177412593 | ||||||
| chr2:177412609
|
T | C | 7 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(4): Show | 7 | HG00735.hp1 HG01891.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-7660T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177412609 | ||||||
| chr2:177412654
|
C | T | 2 | a0001c0001t0023g0074a0001c0001t0023g0075 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.261-7615C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177412654 | ||||||
| chr2:177412824
|
C | G | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.261-7445C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177412824 | ||||||
| chr2:177412940
|
G | A | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.261-7329G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177412940 | ||||||
| chr2:177412975
|
C | T | 228 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(225): Show | 228 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.261-7294C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177412975 | ||||||
| chr2:177413018
|
G | A | 3 | a0001c0001t0002g0032a0001c0001t0002g0087a0001c0001t0040g0040 | 3 | HG01074.hp1 HG02735.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.261-7251G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177413018 | ||||||
| chr2:177413135
|
G | T | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.261-7134G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177413135 | ||||||
| chr2:177413201
|
C | T | 1 | a0001c0001t0033g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.261-7068C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177413201 | ||||||
| chr2:177413269
|
C | G | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.261-7000C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177413269 | ||||||
| chr2:177413469
|
G | A | 2 | a0001c0001t0017g0207a0001c0001t0017g0208 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.261-6800G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177413469 | ||||||
| chr2:177413670
|
A | G | 1 | a0001c0001t0032g0210 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.261-6599A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177413670 | ||||||
| chr2:177413674
|
T | A | 1 | a0001c0001t0003g0229 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.261-6595T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177413674 | ||||||
| chr2:177413679
|
A | T | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.261-6590A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177413679 | ||||||
| chr2:177413713
|
T | C | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.261-6556T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177413713 | ||||||
| chr2:177413760
|
C | T | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.261-6509C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177413760 | ||||||
| chr2:177413889
|
C | T | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.261-6380C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177413889 | ||||||
| chr2:177413917
|
T | C | 7 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(4): Show | 7 | HG00735.hp1 HG01891.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-6352T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177413917 | ||||||
| chr2:177414092
|
T | C | 1 | a0001c0001t0016g0214 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.261-6177T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177414092 | ||||||
| chr2:177414103
|
C | G | 1 | a0001c0001t0001g0176 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.261-6166C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177414103 | ||||||
| chr2:177414235
|
A | G | 2 | a0001c0001t0005g0250a0001c0001t0005g0251 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.261-6034A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177414235 | ||||||
| chr2:177414278
|
C | T | 7 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(4): Show | 7 | HG00735.hp1 HG01891.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-5991C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177414278 | ||||||
| chr2:177414659
|
A | G | 71 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(68): Show | 71 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.261-5610A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177414659 | ||||||
| chr2:177414684
|
A | G | 1 | a0001c0001t0035g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.261-5585A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177414684 | ||||||
| chr2:177414888
|
A | G | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.261-5381A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177414888 | ||||||
| chr2:177414897
|
C | CGT | 4 | a0001c0001t0003g0240a0001c0001t0017g0207a0001c0001t0017g0208others(1): Show | 4 | HG02886.hp2 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-5349_261-5348d others(4): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177414897 | |||||
| chr2:177414897
|
C | CGTGT | 5 | a0001c0001t0002g0023a0001c0001t0002g0039a0001c0001t0002g0041others(2): Show | 5 | NA18963.hp2 NA18965.hp1 NA19087.hp1 others(2): Show |
intron_variant | MODIFIER | c.261-5351_261-5348d others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177414897 | |||||
| chr2:177414897
|
C | CGTGTGT | 70 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(67): Show | 70 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.261-5353_261-5348d others(8): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177414897 | |||||
| chr2:177414897
|
C | CGTGTGTG others(1): Show |
20 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(17): Show | 20 | HG00735.hp1 HG01361.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.261-5355_261-5348d others(10): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177414897 | |||||
| chr2:177414897
|
C | CGTGTGTG others(3): Show |
10 | a0001c0001t0001g0122a0001c0001t0008g0216a0001c0001t0008g0217others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.261-5357_261-5348d others(12): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177414897 | |||||
| chr2:177414897
|
C | CGTGTGTG others(5): Show |
12 | a0001c0001t0001g0117a0001c0001t0001g0127a0001c0001t0001g0252others(9): Show | 12 | HG00408.hp2 HG00735.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.261-5359_261-5348d others(14): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177414897 | |||||
| chr2:177414897
|
C | CGTGTGTG others(7): Show |
81 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(78): Show | 81 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.261-5361_261-5348d others(16): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177414897 | |||||
| chr2:177414897
|
C | CGTGTGTG others(9): Show |
4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0185others(1): Show | 4 | HG00544.hp2 HG00558.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-5363_261-5348d others(18): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177414897 | |||||
| chr2:177414897
|
C | CGTGTGTG others(11): Show |
3 | a0001c0001t0001g0124a0001c0001t0001g0175a0001c0001t0024g0174 | 3 | HG03831.hp1 NA18947.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.261-5365_261-5348d others(20): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177414897 | |||||
| chr2:177414897
|
C | CGTGTGTG others(13): Show |
1 | a0001c0001t0016g0214 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.261-5367_261-5348d others(22): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177414897 | |||||
| chr2:177414897
|
C | CGTGTGTG others(15): Show |
3 | a0001c0001t0016g0212a0001c0001t0049g0001a0001c0001t0050g0001 | 3 | HG02818.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.261-5369_261-5348d others(24): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177414897 | |||||
| chr2:177414897
|
C | CGTGTGTG others(17): Show |
1 | a0001c0001t0016g0213 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.261-5371_261-5348d others(26): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177414897 | |||||
| chr2:177414897
|
C | T | 1 | a0001c0002t0004g0011 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.261-5372C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177414897 | ||||||
| chr2:177414938
|
A | G | 1 | a0001c0001t0006g0073 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.261-5331A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177414938 | ||||||
| chr2:177415112
|
A | T | 1 | a0001c0001t0006g0073 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.261-5157A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177415112 | ||||||
| chr2:177415285
|
T | C | 127 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(124): Show | 127 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.261-4984T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177415285 | ||||||
| chr2:177415303
|
T | C | 130 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(127): Show | 130 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.261-4966T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177415303 | ||||||
| chr2:177415317
|
G | A | 1 | a0001c0001t0002g0030 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.261-4952G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177415317 | ||||||
| chr2:177415348
|
A | G | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.261-4921A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177415348 | ||||||
| chr2:177415381
|
G | A | 2 | a0001c0001t0015g0223a0001c0001t0015g0224 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.261-4888G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177415381 | ||||||
| chr2:177415789
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.261-4480G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177415789 | ||||||
| chr2:177415832
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.261-4437T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177415832 | ||||||
| chr2:177416216
|
A | G | 10 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0066others(7): Show | 10 | HG03831.hp2 NA18943.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.261-4053A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177416216 | ||||||
| chr2:177416496
|
A | G | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.261-3773A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177416496 | ||||||
| chr2:177416516
|
G | T | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.261-3753G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177416516 | ||||||
| chr2:177416517
|
T | G | 1 | a0001c0001t0030g0244 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.261-3752T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177416517 | ||||||
| chr2:177416521
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.261-3748T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177416521 | ||||||
| chr2:177416692
|
A | AT | 7 | a0001c0001t0001g0116a0001c0001t0001g0122a0001c0001t0002g0029others(4): Show | 7 | HG00408.hp1 HG02258.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.261-3566dupT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177416692 | |||||
| chr2:177416743
|
A | C | 1 | a0001c0001t0004g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.261-3526A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177416743 | ||||||
| chr2:177416869
|
G | A | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.261-3400G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177416869 | ||||||
| chr2:177417072
|
C | G | 1 | a0001c0001t0001g0171 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.261-3197C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177417072 | ||||||
| chr2:177417469
|
A | G | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.261-2800A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177417469 | ||||||
| chr2:177417782
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.261-2487G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177417782 | ||||||
| chr2:177418024
|
A | G | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.261-2245A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177418024 | ||||||
| chr2:177418212
|
C | T | 2 | a0001c0001t0021g0027a0001c0001t0021g0028 | 2 | HG00438.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.261-2057C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177418212 | ||||||
| chr2:177418290
|
C | G | 1 | a0001c0001t0010g0170 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.261-1979C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177418290 | ||||||
| chr2:177418295
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.261-1974A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177418295 | ||||||
| chr2:177418389
|
T | C | 73 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.261-1880T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177418389 | ||||||
| chr2:177418456
|
C | G | 1 | a0001c0001t0001g0192 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.261-1813C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177418456 | ||||||
| chr2:177418560
|
A | G | 113 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(110): Show | 113 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.261-1709A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177418560 | ||||||
| chr2:177418728
|
A | G | 1 | a0001c0001t0018g0215 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.261-1541A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177418728 | ||||||
| chr2:177418829
|
T | A | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.261-1440T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177418829 | ||||||
| chr2:177418864
|
C | T | 92 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(89): Show | 92 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.261-1405C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177418864 | ||||||
| chr2:177419051
|
A | T | 6 | a0001c0001t0007g0034a0001c0001t0007g0063a0001c0001t0007g0064others(3): Show | 6 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.261-1218A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177419051 | ||||||
| chr2:177419175
|
A | G | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.261-1094A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177419175 | ||||||
| chr2:177419217
|
ACTTG | A | 70 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(67): Show | 70 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.261-1047_261-1044d others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 177419217 | |||||
| chr2:177419379
|
G | A | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.261-890G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177419379 | ||||||
| chr2:177419598
|
T | C | 1 | a0001c0001t0006g0043 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.261-671T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177419598 | ||||||
| chr2:177419876
|
T | G | 127 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(124): Show | 127 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.261-393T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177419876 | ||||||
| chr2:177419988
|
G | A | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG00544.hp1 HG00597.hp2 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.261-281G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177419988 | ||||||
| chr2:177420094
|
T | C | 4 | a0001c0001t0016g0212a0001c0001t0016g0213a0001c0001t0049g0001others(1): Show | 4 | HG02818.hp1 HG03453.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-175T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177420094 | ||||||
| chr2:177420238
|
G | A | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.261-31G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177420238 | ||||||
| chr2:177420245
|
T | A | 1 | a0001c0001t0008g0219 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.261-24T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177420245 | ||||||
| chr2:177420264
|
A | C | 7 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(4): Show | 7 | HG00735.hp1 HG01891.hp1 HG02895.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.261-5A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 1/19 | chr2 | 177420264 | ||||||
| chr2:177420453
|
G | A | 5 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(2): Show | 5 | HG00735.hp1 HG01891.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.350+95G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177420453 | ||||||
| chr2:177420560
|
G | GTA | 13 | a0001c0001t0001g0129a0001c0002t0004g0002a0001c0002t0004g0003others(10): Show | 13 | HG02055.hp1 HG02602.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.350+212_350+213dup others(2): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 177420560 | |||||
| chr2:177420573
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.350+215A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177420573 | ||||||
| chr2:177420610
|
A | T | 1 | a0001c0001t0020g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.350+252A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177420610 | ||||||
| chr2:177420627
|
C | CA | 5 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.350+273dupA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 177420627 | |||||
| chr2:177420662
|
T | G | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.350+304T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177420662 | ||||||
| chr2:177420999
|
G | T | 164 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(161): Show | 164 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.350+641G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177420999 | ||||||
| chr2:177421083
|
T | C | 127 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(124): Show | 127 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.350+725T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177421083 | ||||||
| chr2:177421205
|
A | G | 2 | a0001c0001t0033g0195a0001c0001t0035g0017 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.350+847A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177421205 | ||||||
| chr2:177421239
|
A | G | 7 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(4): Show | 7 | HG00735.hp1 HG01891.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.350+881A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177421239 | ||||||
| chr2:177421529
|
A | G | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.350+1171A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177421529 | ||||||
| chr2:177421589
|
C | T | 7 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(4): Show | 7 | HG00735.hp1 HG01891.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.350+1231C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177421589 | ||||||
| chr2:177421668
|
G | A | 10 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0097others(7): Show | 10 | HG01361.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.350+1310G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177421668 | ||||||
| chr2:177421734
|
C | T | 236 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(233): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.350+1376C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177421734 | ||||||
| chr2:177421743
|
A | G | 236 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(233): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.350+1385A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177421743 | ||||||
| chr2:177421765
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.350+1407C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177421765 | ||||||
| chr2:177421779
|
C | T | 1 | a0001c0001t0002g0062 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.350+1421C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177421779 | ||||||
| chr2:177421821
|
G | A | 236 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(233): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.350+1463G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177421821 | ||||||
| chr2:177421923
|
A | T | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.350+1565A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177421923 | ||||||
| chr2:177421978
|
G | C | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.350+1620G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177421978 | ||||||
| chr2:177422218
|
G | T | 5 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.350+1860G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177422218 | ||||||
| chr2:177422245
|
G | A | 1 | a0001c0001t0003g0235 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.350+1887G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177422245 | ||||||
| chr2:177422270
|
A | T | 70 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(67): Show | 70 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.350+1912A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177422270 | ||||||
| chr2:177422427
|
TC | T | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.350+2071delC | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 177422427 | |||||
| chr2:177422545
|
G | T | 1 | a0001c0001t0001g0168 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.350+2187G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177422545 | ||||||
| chr2:177422547
|
C | A | 1 | a0001c0001t0001g0168 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.350+2189C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177422547 | ||||||
| chr2:177422635
|
C | T | 1 | a0001c0001t0035g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.350+2277C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177422635 | ||||||
| chr2:177422908
|
TCTACTGA others(403): Show |
T | 127 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(124): Show | 127 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.350+2552_350+2961d others(2): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 177422908 | |||||
| chr2:177423217
|
A | G | 72 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(69): Show | 72 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.350+2859A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177423217 | ||||||
| chr2:177423321
|
A | G | 127 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(124): Show | 127 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.350+2963A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177423321 | ||||||
| chr2:177423322
|
G | C | 127 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(124): Show | 127 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.350+2964G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177423322 | ||||||
| chr2:177423323
|
A | C | 127 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(124): Show | 127 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.350+2965A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177423323 | ||||||
| chr2:177423328
|
ACTGT | A | 127 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(124): Show | 127 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.350+2971_350+2974d others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177423328 | ||||||
| chr2:177423333
|
T | G | 127 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(124): Show | 127 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.350+2975T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177423333 | ||||||
| chr2:177423403
|
T | C | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.350+3045T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177423403 | ||||||
| chr2:177423641
|
C | T | 1 | a0001c0001t0005g0201 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.350+3283C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177423641 | ||||||
| chr2:177423642
|
G | A | 5 | a0001c0001t0001g0111a0001c0001t0001g0130a0001c0001t0001g0131others(2): Show | 5 | HG00423.hp2 HG02027.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.350+3284G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177423642 | ||||||
| chr2:177423881
|
A | T | 1 | a0001c0001t0020g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.350+3523A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177423881 | ||||||
| chr2:177424010
|
C | T | 1 | a0001c0001t0003g0231 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.350+3652C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177424010 | ||||||
| chr2:177424356
|
C | T | 1 | a0001c0001t0004g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.350+3998C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177424356 | ||||||
| chr2:177424452
|
A | AT | 75 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(72): Show | 75 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.350+4105dupT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 177424452 | |||||
| chr2:177424452
|
AT | A | 133 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(130): Show | 133 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.350+4105delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 177424452 | |||||
| chr2:177424452
|
ATT | A | 15 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(12): Show | 15 | HG01361.hp1 HG01884.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.350+4104_350+4105d others(4): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 177424452 | |||||
| chr2:177424493
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.350+4135C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177424493 | ||||||
| chr2:177424629
|
G | T | 105 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(102): Show | 105 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.350+4271G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177424629 | ||||||
| chr2:177424771
|
C | T | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.350+4413C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177424771 | ||||||
| chr2:177424928
|
G | T | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.350+4570G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177424928 | ||||||
| chr2:177425028
|
T | C | 2 | a0001c0001t0003g0230a0001c0001t0003g0231 | 2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.350+4670T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177425028 | ||||||
| chr2:177425347
|
G | A | 1 | a0001c0001t0033g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.350+4989G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177425347 | ||||||
| chr2:177425471
|
A | G | 130 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(127): Show | 130 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.350+5113A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177425471 | ||||||
| chr2:177425479
|
G | A | 108 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(105): Show | 108 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.350+5121G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177425479 | ||||||
| chr2:177425490
|
G | A | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.350+5132G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177425490 | ||||||
| chr2:177425513
|
C | T | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.350+5155C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177425513 | ||||||
| chr2:177425514
|
A | G | 236 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(233): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.350+5156A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177425514 | ||||||
| chr2:177425622
|
G | GA | 175 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0103others(172): Show | 175 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.350+5286dupA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 177425622 | |||||
| chr2:177425622
|
G | GAA | 32 | a0001c0001t0001g0112a0001c0001t0001g0133a0001c0001t0001g0172others(29): Show | 32 | HG00673.hp2 HG01169.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.350+5285_350+5286d others(4): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 177425622 | |||||
| chr2:177425622
|
GAAAAAA | G | 11 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0097others(8): Show | 11 | HG01361.hp1 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.350+5281_350+5286d others(8): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 177425622 | |||||
| chr2:177425623
|
A | G | 2 | a0001c0001t0017g0207a0001c0001t0017g0208 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.350+5265A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177425623 | ||||||
| chr2:177425723
|
G | T | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.350+5365G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177425723 | ||||||
| chr2:177425739
|
C | T | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.350+5381C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177425739 | ||||||
| chr2:177425830
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.350+5472C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177425830 | ||||||
| chr2:177426224
|
A | G | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.350+5866A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177426224 | ||||||
| chr2:177426301
|
G | A | 238 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(235): Show | 238 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(235): Show |
intron_variant | MODIFIER | c.350+5943G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177426301 | ||||||
| chr2:177426487
|
C | T | 1 | a0001c0001t0003g0239 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.350+6129C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177426487 | ||||||
| chr2:177426531
|
G | A | 1 | a0001c0001t0005g0200 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.350+6173G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177426531 | ||||||
| chr2:177426544
|
C | T | 2 | a0001c0001t0033g0195a0001c0001t0035g0017 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.350+6186C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177426544 | ||||||
| chr2:177426763
|
G | A | 3 | a0001c0003t0001g0255a0001c0003t0005g0256a0001c0003t0005g0257 | 3 | HG02258.hp1 HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.350+6405G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177426763 | ||||||
| chr2:177426770
|
A | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.350+6412A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177426770 | ||||||
| chr2:177426913
|
T | C | 73 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.350+6555T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177426913 | ||||||
| chr2:177427137
|
T | A | 1 | a0001c0001t0001g0136 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.350+6779T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177427137 | ||||||
| chr2:177427145
|
A | G | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.350+6787A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177427145 | ||||||
| chr2:177427403
|
T | C | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.351-6924T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177427403 | ||||||
| chr2:177427675
|
C | T | 73 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.351-6652C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177427675 | ||||||
| chr2:177427693
|
G | C | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.351-6634G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177427693 | ||||||
| chr2:177427734
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.351-6593G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177427734 | ||||||
| chr2:177427754
|
G | A | 3 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121 | 3 | NA19058.hp2 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.351-6573G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177427754 | ||||||
| chr2:177428276
|
C | T | 7 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(4): Show | 7 | HG01109.hp1 HG01243.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.351-6051C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177428276 | ||||||
| chr2:177428303
|
C | T | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.351-6024C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177428303 | ||||||
| chr2:177428496
|
G | T | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.351-5831G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177428496 | ||||||
| chr2:177428567
|
C | T | 115 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(112): Show | 115 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.351-5760C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177428567 | ||||||
| chr2:177428568
|
G | A | 1 | a0001c0001t0006g0082 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.351-5759G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177428568 | ||||||
| chr2:177428910
|
T | C | 1 | a0001c0001t0002g0087 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.351-5417T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177428910 | ||||||
| chr2:177429002
|
T | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | NA18945.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.351-5325T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177429002 | ||||||
| chr2:177429192
|
C | T | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.351-5135C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177429192 | ||||||
| chr2:177429377
|
A | C | 1 | a0001c0001t0002g0031 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.351-4950A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177429377 | ||||||
| chr2:177429378
|
G | A | 1 | a0001c0001t0013g0188 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.351-4949G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177429378 | ||||||
| chr2:177429920
|
G | A | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.351-4407G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177429920 | ||||||
| chr2:177430240
|
C | G | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG00642.hp1 HG01257.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.351-4087C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177430240 | ||||||
| chr2:177430393
|
G | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.351-3934G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177430393 | ||||||
| chr2:177430454
|
G | A | 236 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(233): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.351-3873G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177430454 | ||||||
| chr2:177430758
|
C | T | 2 | a0001c0001t0005g0250a0001c0001t0005g0251 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.351-3569C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177430758 | ||||||
| chr2:177430845
|
C | T | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.351-3482C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177430845 | ||||||
| chr2:177431086
|
T | C | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.351-3241T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177431086 | ||||||
| chr2:177431431
|
G | A | 1 | a0001c0001t0037g0019 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.351-2896G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177431431 | ||||||
| chr2:177431735
|
G | A | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.351-2592G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177431735 | ||||||
| chr2:177431897
|
A | G | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.351-2430A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177431897 | ||||||
| chr2:177432044
|
A | G | 233 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(230): Show | 233 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.351-2283A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177432044 | ||||||
| chr2:177432177
|
A | G | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.351-2150A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177432177 | ||||||
| chr2:177432193
|
T | G | 1 | a0001c0001t0020g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.351-2134T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177432193 | ||||||
| chr2:177432196
|
G | A | 7 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(4): Show | 7 | HG01109.hp1 HG01243.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.351-2131G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177432196 | ||||||
| chr2:177432234
|
A | G | 1 | a0001c0001t0016g0213 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.351-2093A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177432234 | ||||||
| chr2:177432267
|
A | G | 5 | a0001c0001t0012g0014a0001c0001t0012g0015a0001c0001t0012g0016others(2): Show | 5 | HG02258.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.351-2060A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177432267 | ||||||
| chr2:177432613
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.351-1714G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177432613 | ||||||
| chr2:177432801
|
T | G | 1 | a0001c0001t0015g0225 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.351-1526T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177432801 | ||||||
| chr2:177432851
|
G | A | 1 | a0001c0001t0026g0236 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.351-1476G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177432851 | ||||||
| chr2:177432934
|
C | T | 2 | a0001c0001t0002g0072a0001c0001t0002g0080 | 2 | NA18966.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.351-1393C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177432934 | ||||||
| chr2:177433012
|
C | T | 76 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(73): Show | 76 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.351-1315C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177433012 | ||||||
| chr2:177433206
|
C | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0140 | 2 | HG00735.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.351-1121C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177433206 | ||||||
| chr2:177433376
|
G | A | 160 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(157): Show | 160 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.351-951G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177433376 | ||||||
| chr2:177433599
|
A | G | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.351-728A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177433599 | ||||||
| chr2:177433924
|
A | T | 1 | a0001c0001t0002g0071 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.351-403A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177433924 | ||||||
| chr2:177433959
|
T | C | 160 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(157): Show | 160 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.351-368T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177433959 | ||||||
| chr2:177434129
|
T | G | 3 | a0001c0001t0012g0014a0001c0001t0012g0015a0001c0001t0012g0016 | 3 | HG02258.hp2 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.351-198T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177434129 | ||||||
| chr2:177434133
|
G | A | 70 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(67): Show | 70 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.351-194G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177434133 | ||||||
| chr2:177434269
|
G | A | 1 | a0001c0001t0046g0209 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.351-58G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 2/19 | chr2 | 177434269 | ||||||
| chr2:177434494
|
T | G | 1 | a0001c0001t0001g0118 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.441+77T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177434494 | ||||||
| chr2:177434546
|
T | G | 1 | a0001c0001t0001g0178 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.441+129T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177434546 | ||||||
| chr2:177434777
|
C | A | 13 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(10): Show | 13 | HG01361.hp1 HG01884.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+360C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177434777 | ||||||
| chr2:177434995
|
A | AGG | 4 | a0001c0001t0001g0167a0001c0001t0012g0014a0001c0001t0012g0015others(1): Show | 4 | HG02258.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+579_441+580dup others(2): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr2 | 177434995 | |||||
| chr2:177434997
|
G | GGGTA | 7 | a0001c0001t0001g0103a0001c0001t0001g0165a0001c0001t0008g0218others(4): Show | 7 | HG01109.hp1 HG01361.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.441+580_441+581ins others(4): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177434997 | ||||||
| chr2:177434997
|
G | GGGTATA | 61 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0110others(58): Show | 61 | HG00639.hp2 HG00642.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.441+580_441+581ins others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177434997 | ||||||
| chr2:177434997
|
G | GGGTATAT others(1): Show |
29 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0108others(26): Show | 29 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.441+580_441+581ins others(8): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177434997 | ||||||
| chr2:177434997
|
G | GGGTATAT others(3): Show |
15 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(12): Show | 15 | HG00544.hp2 HG00558.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+580_441+581ins others(10): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177434997 | ||||||
| chr2:177434997
|
G | GGGTATAT others(5): Show |
8 | a0001c0001t0001g0112a0001c0001t0001g0137a0001c0001t0001g0141others(5): Show | 8 | HG00438.hp2 HG00735.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.441+580_441+581ins others(12): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177434997 | ||||||
| chr2:177434997
|
G | GGGTATAT others(7): Show |
2 | a0001c0001t0001g0136a0001c0001t0037g0019 | 2 | HG03704.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.441+580_441+581ins others(14): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177434997 | ||||||
| chr2:177434997
|
G | GGGTATAT others(9): Show |
2 | a0001c0001t0001g0097a0001c0001t0001g0107 | 2 | HG03540.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.441+580_441+581ins others(16): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177434997 | ||||||
| chr2:177434997
|
G | GGGTATAT others(11): Show |
3 | a0001c0001t0005g0104a0001c0001t0016g0214a0001c0002t0013g0206 | 3 | HG02055.hp2 HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.441+580_441+581ins others(18): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177434997 | ||||||
| chr2:177434997
|
G | GGGTATAT others(13): Show |
1 | a0001c0001t0001g0092 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.441+580_441+581ins others(20): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177434997 | ||||||
| chr2:177434997
|
G | GGGTGTAT others(11): Show |
1 | a0001c0001t0013g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.441+580_441+581ins others(18): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177434997 | ||||||
| chr2:177434997
|
G | GTA | 18 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0061others(15): Show | 18 | HG00642.hp2 HG01081.hp2 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.441+606_441+607dup others(2): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr2 | 177434997 | |||||
| chr2:177434997
|
G | GTATA | 51 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0029others(48): Show | 51 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.441+604_441+607dup others(4): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr2 | 177434997 | |||||
| chr2:177434997
|
G | GTATATA | 19 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0031others(16): Show | 19 | HG00738.hp2 HG01074.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.441+602_441+607dup others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr2 | 177434997 | |||||
| chr2:177434997
|
G | GTATATAT others(1): Show |
14 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0079others(11): Show | 14 | HG00423.hp1 HG01258.hp1 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.441+600_441+607dup others(8): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr2 | 177434997 | |||||
| chr2:177434997
|
G | GTATATAT others(3): Show |
7 | a0001c0001t0002g0037a0001c0001t0025g0253a0001c0001t0025g0254others(4): Show | 7 | HG01255.hp1 HG01257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+598_441+607dup others(10): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr2 | 177434997 | |||||
| chr2:177434997
|
G | GTATATAT others(5): Show |
2 | a0001c0001t0002g0249a0001c0002t0048g0008 | 2 | HG02074.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.441+596_441+607dup others(12): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr2 | 177434997 | |||||
| chr2:177434997
|
G | GTATATAT others(9): Show |
1 | a0001c0002t0004g0012 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.441+592_441+607dup others(16): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr2 | 177434997 | |||||
| chr2:177434997
|
G | GTATATAT others(11): Show |
1 | a0001c0003t0001g0255 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.441+590_441+607dup others(18): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr2 | 177434997 | |||||
| chr2:177434997
|
GTATATAT others(9): Show |
G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.441+592_441+607del others(16): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr2 | 177434997 | |||||
| chr2:177434998
|
T | G | 1 | a0001c0001t0001g0118 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.441+581T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177434998 | ||||||
| chr2:177434999
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.441+582A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177434999 | ||||||
| chr2:177435050
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0100 | 2 | HG01361.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.441+633G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177435050 | ||||||
| chr2:177435224
|
A | T | 1 | a0001c0001t0002g0060 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.441+807A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177435224 | ||||||
| chr2:177435774
|
G | A | 1 | a0001c0001t0003g0229 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.442-990G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177435774 | ||||||
| chr2:177435787
|
C | G | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.442-977C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177435787 | ||||||
| chr2:177436118
|
T | C | 13 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(10): Show | 13 | HG01361.hp1 HG01884.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.442-646T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177436118 | ||||||
| chr2:177436139
|
A | ATTTTT | 13 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0002t0004g0003others(10): Show | 13 | HG02258.hp1 HG02280.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.442-610_442-606dup others(5): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr2 | 177436139 | |||||
| chr2:177436139
|
A | ATTTTTT | 8 | a0001c0001t0002g0049a0001c0001t0002g0090a0001c0001t0017g0207others(5): Show | 8 | HG02027.hp2 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-611_442-606dup others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr2 | 177436139 | |||||
| chr2:177436139
|
A | ATTTTTTT | 50 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(47): Show | 50 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.442-612_442-606dup others(7): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr2 | 177436139 | |||||
| chr2:177436139
|
A | ATTTTTTT others(1): Show |
22 | a0001c0001t0001g0186a0001c0001t0002g0023a0001c0001t0002g0031others(19): Show | 22 | HG00423.hp1 HG00597.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.442-613_442-606dup others(8): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr2 | 177436139 | |||||
| chr2:177436139
|
A | ATTTTTTT others(2): Show |
72 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(69): Show | 72 | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.442-614_442-606dup others(9): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr2 | 177436139 | |||||
| chr2:177436139
|
A | ATTTTTTT others(3): Show |
47 | a0001c0001t0001g0095a0001c0001t0001g0100a0001c0001t0001g0103others(44): Show | 47 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.442-615_442-606dup others(10): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr2 | 177436139 | |||||
| chr2:177436139
|
A | ATTTTTTT others(4): Show |
14 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0096others(11): Show | 14 | HG01168.hp1 HG01361.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.442-616_442-606dup others(11): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr2 | 177436139 | |||||
| chr2:177436139
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0012g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.442-617_442-606dup others(12): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr2 | 177436139 | |||||
| chr2:177436244
|
C | T | 10 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0066others(7): Show | 10 | HG03831.hp2 NA18943.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.442-520C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177436244 | ||||||
| chr2:177436296
|
C | A | 7 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(4): Show | 7 | HG00735.hp1 HG01891.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-468C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177436296 | ||||||
| chr2:177436439
|
T | C | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.442-325T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177436439 | ||||||
| chr2:177436472
|
A | G | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-292A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177436472 | ||||||
| chr2:177436676
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.442-88G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177436676 | ||||||
| chr2:177436700
|
C | T | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.442-64C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 3/19 | chr2 | 177436700 | ||||||
| chr2:177437126
|
G | A | 1 | a0001c0001t0005g0200 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.637+72G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177437126 | ||||||
| chr2:177437329
|
A | G | 72 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(69): Show | 72 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.637+275A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177437329 | ||||||
| chr2:177437684
|
T | C | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.637+630T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177437684 | ||||||
| chr2:177437770
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.637+716A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177437770 | ||||||
| chr2:177437870
|
G | A | 5 | a0001c0001t0002g0050a0001c0001t0002g0053a0001c0001t0002g0057others(2): Show | 5 | HG02074.hp2 NA18941.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+816G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177437870 | ||||||
| chr2:177438096
|
A | G | 1 | a0001c0002t0009g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.637+1042A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177438096 | ||||||
| chr2:177438624
|
A | G | 2 | a0001c0001t0033g0195a0001c0001t0035g0017 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.637+1570A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177438624 | ||||||
| chr2:177438672
|
G | C | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.637+1618G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177438672 | ||||||
| chr2:177438821
|
A | C | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+1767A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177438821 | ||||||
| chr2:177438983
|
T | TAC | 4 | a0001c0001t0003g0239a0001c0001t0015g0223a0001c0001t0015g0224others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+1949_637+1950d others(4): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr2 | 177438983 | |||||
| chr2:177438983
|
T | TACAC | 136 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(133): Show | 136 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.637+1947_637+1950d others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr2 | 177438983 | |||||
| chr2:177438983
|
T | TACACAC | 25 | a0001c0001t0001g0142a0001c0001t0001g0183a0001c0001t0002g0024others(22): Show | 25 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.637+1945_637+1950d others(8): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr2 | 177438983 | |||||
| chr2:177438983
|
T | TACACACA others(1): Show |
68 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0029others(65): Show | 68 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.637+1943_637+1950d others(10): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr2 | 177438983 | |||||
| chr2:177438983
|
T | TACACACA others(3): Show |
3 | a0001c0001t0020g0196a0001c0001t0033g0195a0001c0001t0035g0017 | 3 | HG03486.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.637+1941_637+1950d others(12): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr2 | 177438983 | |||||
| chr2:177438983
|
T | TACGCACA others(5): Show |
4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+1931_637+1932i others(14): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr2 | 177438983 | |||||
| chr2:177439096
|
T | C | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.638-1869T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177439096 | ||||||
| chr2:177439169
|
G | C | 6 | a0001c0001t0015g0223a0001c0001t0015g0224a0001c0001t0015g0225others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.638-1796G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177439169 | ||||||
| chr2:177439194
|
G | C | 236 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(233): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.638-1771G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177439194 | ||||||
| chr2:177439247
|
A | G | 5 | a0001c0001t0012g0014a0001c0001t0012g0015a0001c0001t0012g0016others(2): Show | 5 | HG02258.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-1718A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177439247 | ||||||
| chr2:177439253
|
C | T | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.638-1712C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177439253 | ||||||
| chr2:177439274
|
C | G | 2 | a0001c0001t0033g0195a0001c0001t0035g0017 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.638-1691C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177439274 | ||||||
| chr2:177439587
|
G | T | 3 | a0001c0001t0012g0014a0001c0001t0012g0015a0001c0001t0012g0016 | 3 | HG02258.hp2 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.638-1378G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177439587 | ||||||
| chr2:177439638
|
T | C | 2 | a0001c0001t0018g0215a0001c0001t0018g0221 | 2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.638-1327T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177439638 | ||||||
| chr2:177439890
|
T | C | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.638-1075T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177439890 | ||||||
| chr2:177440041
|
G | C | 1 | a0001c0001t0001g0185 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.638-924G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177440041 | ||||||
| chr2:177440140
|
A | T | 2 | a0001c0001t0002g0053a0001c0001t0002g0249 | 2 | HG02074.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.638-825A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177440140 | ||||||
| chr2:177440151
|
C | CCACTACA others(3): Show |
1 | a0001c0001t0001g0186 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.638-809_638-808ins others(10): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr2 | 177440151 | |||||
| chr2:177440157
|
T | C | 136 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(133): Show | 136 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.638-808T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177440157 | ||||||
| chr2:177440322
|
T | G | 1 | a0001c0001t0001g0184 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.638-643T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177440322 | ||||||
| chr2:177440551
|
C | T | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.638-414C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177440551 | ||||||
| chr2:177440709
|
A | G | 230 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(227): Show | 230 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.638-256A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177440709 | ||||||
| chr2:177440792
|
A | G | 1 | a0001c0001t0040g0040 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.638-173A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 5/19 | chr2 | 177440792 | ||||||
| chr2:177441256
|
G | A | 1 | a0001c0001t0032g0210 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.709+220G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 6/19 | chr2 | 177441256 | ||||||
| chr2:177441353
|
T | G | 1 | a0001c0001t0002g0051 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.709+317T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 6/19 | chr2 | 177441353 | ||||||
| chr2:177441783
|
A | G | 2 | a0001c0001t0005g0250a0001c0001t0005g0251 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.710-624A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 6/19 | chr2 | 177441783 | ||||||
| chr2:177441856
|
A | G | 105 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(102): Show | 105 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.710-551A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 6/19 | chr2 | 177441856 | ||||||
| chr2:177441874
|
C | A | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.710-533C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 6/19 | chr2 | 177441874 | ||||||
| chr2:177442261
|
A | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.710-146A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 6/19 | chr2 | 177442261 | ||||||
| chr2:177442321
|
T | A | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.710-86T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 6/19 | chr2 | 177442321 | ||||||
| chr2:177442342
|
G | T | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.710-65G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 6/19 | chr2 | 177442342 | ||||||
| chr2:177442572
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.789+86C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177442572 | ||||||
| chr2:177442602
|
C | T | 164 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(161): Show | 164 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.789+116C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177442602 | ||||||
| chr2:177442656
|
G | C | 2 | a0001c0001t0006g0044a0001c0001t0006g0082 | 2 | NA19058.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.789+170G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177442656 | ||||||
| chr2:177442731
|
C | T | 1 | a0001c0003t0005g0257 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.789+245C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177442731 | ||||||
| chr2:177442765
|
T | C | 3 | a0001c0001t0002g0030a0001c0001t0002g0058a0001c0001t0002g0060 | 3 | NA18950.hp1 NA18998.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.789+279T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177442765 | ||||||
| chr2:177442828
|
C | CAA | 5 | a0001c0001t0006g0043a0001c0001t0011g0245a0001c0001t0011g0246others(2): Show | 5 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+361_789+362dup others(2): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr2 | 177442828 | |||||
| chr2:177442828
|
CA | C | 144 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(141): Show | 144 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.789+362delA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr2 | 177442828 | |||||
| chr2:177442855
|
A | G | 7 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(4): Show | 7 | HG01109.hp1 HG01243.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.789+369A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177442855 | ||||||
| chr2:177443709
|
C | T | 1 | a0001c0001t0016g0214 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.789+1223C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177443709 | ||||||
| chr2:177444002
|
G | GAT | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.789+1526_789+1527d others(4): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr2 | 177444002 | |||||
| chr2:177444158
|
C | T | 4 | a0001c0001t0015g0223a0001c0001t0015g0224a0001c0001t0015g0225others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-1388C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177444158 | ||||||
| chr2:177444178
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.790-1368T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177444178 | ||||||
| chr2:177444230
|
G | C | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.790-1316G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177444230 | ||||||
| chr2:177444279
|
T | G | 160 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(157): Show | 160 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.790-1267T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177444279 | ||||||
| chr2:177444420
|
C | CA | 10 | a0001c0001t0001g0109a0001c0001t0001g0129a0001c0001t0001g0171others(7): Show | 10 | HG01074.hp2 HG01109.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.790-1106dupA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr2 | 177444420 | |||||
| chr2:177444420
|
CA | C | 8 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0179others(5): Show | 8 | HG01081.hp2 HG01168.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.790-1106delA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr2 | 177444420 | |||||
| chr2:177444420
|
CAA | C | 104 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.790-1107_790-1106d others(4): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr2 | 177444420 | |||||
| chr2:177444420
|
CAAA | C | 29 | a0001c0001t0003g0231a0001c0001t0004g0093a0001c0001t0011g0245others(26): Show | 29 | HG02055.hp1 HG02132.hp1 HG02165.hp1 others(26): Show |
intron_variant | MODIFIER | c.790-1108_790-1106d others(5): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr2 | 177444420 | |||||
| chr2:177444475
|
GTATAAT | G | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.790-1067_790-1062d others(8): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr2 | 177444475 | |||||
| chr2:177444511
|
G | C | 5 | a0001c0001t0016g0212a0001c0001t0016g0213a0001c0001t0016g0214others(2): Show | 5 | HG02055.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.790-1035G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177444511 | ||||||
| chr2:177444552
|
G | A | 7 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(4): Show | 7 | HG01109.hp1 HG01243.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.790-994G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177444552 | ||||||
| chr2:177444617
|
TTTTTGTA others(5): Show |
T | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.790-917_790-906del others(12): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr2 | 177444617 | |||||
| chr2:177444646
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.790-900G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177444646 | ||||||
| chr2:177444691
|
A | T | 228 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(225): Show | 228 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.790-855A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177444691 | ||||||
| chr2:177444823
|
T | C | 1 | a0001c0001t0013g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.790-723T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177444823 | ||||||
| chr2:177444836
|
A | G | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-710A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177444836 | ||||||
| chr2:177444967
|
T | A | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.790-579T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177444967 | ||||||
| chr2:177445029
|
A | G | 1 | a0001c0001t0030g0244 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.790-517A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177445029 | ||||||
| chr2:177445120
|
T | A | 108 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(105): Show | 108 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.790-426T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177445120 | ||||||
| chr2:177445281
|
A | C | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-265A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177445281 | ||||||
| chr2:177445477
|
G | A | 1 | a0001c0001t0013g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.790-69G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 7/19 | chr2 | 177445477 | ||||||
| chr2:177445853
|
G | A | 4 | a0001c0001t0015g0223a0001c0001t0015g0224a0001c0001t0015g0225others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+227G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177445853 | ||||||
| chr2:177446148
|
A | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.870+522A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177446148 | ||||||
| chr2:177446149
|
CT | C | 236 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(233): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.870+536delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177446149 | |||||
| chr2:177446198
|
G | A | 1 | a0001c0001t0024g0098 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.870+572G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177446198 | ||||||
| chr2:177446222
|
C | T | 4 | a0001c0001t0003g0234a0001c0001t0003g0239a0001c0001t0026g0236others(1): Show | 4 | HG00642.hp2 HG01168.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+596C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177446222 | ||||||
| chr2:177446293
|
A | G | 1 | a0001c0001t0033g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.870+667A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177446293 | ||||||
| chr2:177446575
|
A | G | 3 | a0001c0001t0012g0014a0001c0001t0012g0015a0001c0001t0012g0016 | 3 | HG02258.hp2 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.870+949A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177446575 | ||||||
| chr2:177446593
|
C | T | 1 | a0001c0001t0003g0229 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.870+967C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177446593 | ||||||
| chr2:177446781
|
A | G | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.870+1155A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177446781 | ||||||
| chr2:177447231
|
A | G | 2 | a0001c0001t0003g0230a0001c0001t0003g0231 | 2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.870+1605A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177447231 | ||||||
| chr2:177447271
|
T | C | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.870+1645T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177447271 | ||||||
| chr2:177447448
|
A | C | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.870+1822A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177447448 | ||||||
| chr2:177447602
|
CT | C | 73 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.870+1988delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177447602 | |||||
| chr2:177447639
|
A | G | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2013A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177447639 | ||||||
| chr2:177447930
|
G | A | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.870+2304G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177447930 | ||||||
| chr2:177447944
|
A | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0179 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.870+2318A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177447944 | ||||||
| chr2:177448187
|
G | T | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2561G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177448187 | ||||||
| chr2:177448264
|
G | A | 1 | a0001c0001t0009g0091 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.870+2638G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177448264 | ||||||
| chr2:177448533
|
A | T | 2 | a0001c0001t0017g0207a0001c0001t0017g0208 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.870+2907A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177448533 | ||||||
| chr2:177448535
|
A | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.870+2909A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177448535 | ||||||
| chr2:177448731
|
C | T | 1 | a0001c0001t0003g0233 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.870+3105C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177448731 | ||||||
| chr2:177448836
|
C | A | 71 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(68): Show | 71 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.870+3210C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177448836 | ||||||
| chr2:177448890
|
A | G | 234 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(231): Show | 234 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.870+3264A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177448890 | ||||||
| chr2:177449298
|
A | G | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.870+3672A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177449298 | ||||||
| chr2:177449333
|
C | A | 1 | a0001c0001t0002g0049 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.870+3707C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177449333 | ||||||
| chr2:177449333
|
C | T | 4 | a0001c0001t0016g0212a0001c0001t0016g0213a0001c0001t0049g0001others(1): Show | 4 | HG02818.hp1 HG03453.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+3707C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177449333 | ||||||
| chr2:177449362
|
C | T | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.870+3736C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177449362 | ||||||
| chr2:177449432
|
T | C | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.870+3806T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177449432 | ||||||
| chr2:177449461
|
T | C | 4 | a0001c0001t0001g0118a0001c0001t0001g0127a0001c0001t0001g0178others(1): Show | 4 | HG00639.hp2 HG01081.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+3835T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177449461 | ||||||
| chr2:177449628
|
T | C | 12 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.870+4002T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177449628 | ||||||
| chr2:177449931
|
G | A | 3 | a0001c0001t0001g0193a0001c0001t0017g0207a0001c0001t0017g0208 | 3 | HG02922.hp1 HG03195.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.870+4305G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177449931 | ||||||
| chr2:177449998
|
T | C | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.870+4372T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177449998 | ||||||
| chr2:177449999
|
G | A | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.870+4373G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177449999 | ||||||
| chr2:177450117
|
G | A | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.870+4491G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177450117 | ||||||
| chr2:177450462
|
T | C | 2 | a0001c0001t0022g0134a0001c0001t0022g0135 | 2 | HG00673.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.870+4836T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177450462 | ||||||
| chr2:177450633
|
A | G | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.870+5007A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177450633 | ||||||
| chr2:177450797
|
G | T | 1 | a0001c0001t0013g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.870+5171G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177450797 | ||||||
| chr2:177450816
|
T | C | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.870+5190T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177450816 | ||||||
| chr2:177450963
|
C | CATATATA others(21): Show |
4 | a0001c0002t0004g0002a0001c0002t0004g0003a0001c0002t0004g0007others(1): Show | 4 | HG02055.hp1 HG02965.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+5349_870+5350i others(30): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450963 | |||||
| chr2:177450963
|
C | CATATATA others(23): Show |
1 | a0001c0002t0004g0006 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.870+5349_870+5350i others(32): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450963 | |||||
| chr2:177450963
|
C | CATATATA others(25): Show |
2 | a0001c0002t0004g0004a0001c0002t0004g0005 | 2 | HG03130.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.870+5349_870+5350i others(34): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450963 | |||||
| chr2:177450963
|
C | CATATATA others(29): Show |
5 | a0001c0002t0004g0009a0001c0002t0004g0011a0001c0002t0004g0013others(2): Show | 5 | HG02486.hp1 HG02602.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.870+5349_870+5350i others(38): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450963 | |||||
| chr2:177450963
|
C | CATATATA others(31): Show |
4 | a0001c0001t0025g0253a0001c0001t0025g0254a0001c0002t0004g0012others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+5349_870+5350i others(40): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450963 | |||||
| chr2:177450963
|
C | CATATATA others(33): Show |
1 | a0001c0003t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.870+5349_870+5350i others(42): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450963 | |||||
| chr2:177450963
|
C | CATATATA others(35): Show |
1 | a0001c0001t0004g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.870+5349_870+5350i others(44): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450963 | |||||
| chr2:177450964
|
A | ATATATAT others(21): Show |
3 | a0001c0001t0012g0014a0001c0001t0012g0015a0001c0001t0012g0016 | 3 | HG02258.hp2 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.870+5346_870+5347i others(30): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(21): Show |
12 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.870+5348_870+5349i others(30): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(49): Show |
1 | a0001c0002t0013g0206 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.870+5349_870+5350i others(58): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(57): Show |
1 | a0001c0002t0009g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.870+5349_870+5350i others(66): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(65): Show |
1 | a0001c0002t0034g0211 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.870+5349_870+5350i others(74): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0035g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.870+5349_870+5350i others(36): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(27): Show |
91 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(88): Show | 91 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.870+5349_870+5350i others(36): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(29): Show |
1 | a0001c0001t0024g0174 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.870+5349_870+5350i others(38): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(27): Show |
18 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231others(15): Show | 18 | HG01081.hp2 HG01168.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.870+5349_870+5350i others(36): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(29): Show |
4 | a0001c0001t0003g0234a0001c0001t0015g0223a0001c0001t0015g0224others(1): Show | 4 | HG00642.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+5349_870+5350i others(38): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(35): Show |
1 | a0001c0001t0002g0061 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.870+5349_870+5350i others(44): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(51): Show |
1 | a0001c0001t0006g0043 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.870+5349_870+5350i others(60): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(49): Show |
3 | a0001c0001t0006g0045a0001c0001t0006g0073a0001c0001t0036g0046 | 3 | HG00544.hp1 HG00597.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.870+5349_870+5350i others(58): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(51): Show |
1 | a0001c0001t0002g0042 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.870+5349_870+5350i others(60): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(47): Show |
2 | a0001c0001t0014g0020a0001c0001t0014g0022 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.870+5349_870+5350i others(56): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(53): Show |
8 | a0001c0001t0002g0037a0001c0001t0002g0039a0001c0001t0002g0060others(5): Show | 8 | HG00609.hp2 HG01257.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.870+5349_870+5350i others(62): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(53): Show |
1 | a0001c0001t0037g0019 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.870+5349_870+5350i others(62): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(55): Show |
15 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0050others(12): Show | 15 | HG00639.hp1 HG01928.hp2 HG02735.hp1 others(12): Show |
intron_variant | MODIFIER | c.870+5349_870+5350i others(64): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(55): Show |
1 | a0001c0001t0005g0201 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.870+5349_870+5350i others(64): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(53): Show |
1 | a0001c0001t0001g0203 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.870+5349_870+5350i others(62): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(59): Show |
1 | a0001c0001t0013g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.870+5349_870+5350i others(68): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(57): Show |
18 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0041others(15): Show | 18 | HG00423.hp1 HG00558.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.870+5349_870+5350i others(66): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(57): Show |
3 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0200 | 3 | HG00735.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.870+5349_870+5350i others(66): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(55): Show |
1 | a0001c0001t0033g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.870+5349_870+5350i others(64): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(55): Show |
4 | a0001c0001t0001g0095a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG02559.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+5349_870+5350i others(64): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(59): Show |
14 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0029others(11): Show | 14 | HG00408.hp1 HG00738.hp2 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.870+5349_870+5350i others(68): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(59): Show |
1 | a0001c0001t0005g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.870+5349_870+5350i others(68): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(57): Show |
1 | a0001c0001t0020g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.870+5349_870+5350i others(66): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(57): Show |
7 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0097others(4): Show | 7 | HG02895.hp2 HG02897.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.870+5349_870+5350i others(66): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(55): Show |
1 | a0001c0001t0017g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.870+5349_870+5350i others(64): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(61): Show |
2 | a0001c0001t0002g0054a0001c0001t0006g0082 | 2 | HG01496.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.870+5349_870+5350i others(70): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(59): Show |
1 | a0001c0001t0001g0103 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.870+5349_870+5350i others(68): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(57): Show |
2 | a0001c0001t0017g0208a0001c0001t0046g0209 | 2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.870+5349_870+5350i others(66): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(63): Show |
5 | a0001c0001t0002g0058a0001c0001t0002g0067a0001c0001t0002g0068others(2): Show | 5 | HG00438.hp1 NA18943.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.870+5349_870+5350i others(72): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(61): Show |
2 | a0001c0001t0005g0104a0001c0001t0024g0098 | 2 | HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.870+5349_870+5350i others(70): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(65): Show |
1 | a0001c0001t0002g0080 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.870+5349_870+5350i others(74): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(61): Show |
1 | a0001c0001t0014g0021 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.870+5349_870+5350i others(70): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(67): Show |
1 | a0001c0001t0002g0069 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.870+5349_870+5350i others(76): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATATATAT others(65): Show |
2 | a0001c0001t0001g0096a0001c0001t0001g0100 | 2 | HG01361.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.870+5349_870+5350i others(74): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177450964
|
A | ATTCATAT others(59): Show |
4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+5339_870+5340i others(68): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177450964 | |||||
| chr2:177451023
|
A | G | 92 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(89): Show | 92 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.870+5397A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177451023 | ||||||
| chr2:177451088
|
G | A | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.870+5462G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177451088 | ||||||
| chr2:177451171
|
G | A | 134 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(131): Show | 134 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.870+5545G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177451171 | ||||||
| chr2:177451364
|
T | C | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.870+5738T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177451364 | ||||||
| chr2:177451512
|
C | T | 1 | a0001c0001t0002g0087 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.870+5886C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177451512 | ||||||
| chr2:177451578
|
C | T | 1 | a0001c0002t0004g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.870+5952C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177451578 | ||||||
| chr2:177451627
|
A | G | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.870+6001A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177451627 | ||||||
| chr2:177451628
|
A | C | 3 | a0001c0002t0009g0204a0001c0002t0013g0206a0001c0002t0034g0211 | 3 | HG02109.hp1 HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.870+6002A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177451628 | ||||||
| chr2:177451699
|
A | G | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.870+6073A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177451699 | ||||||
| chr2:177451868
|
A | G | 3 | a0001c0001t0002g0037a0001c0001t0002g0059a0001c0001t0002g0079 | 3 | HG01257.hp1 HG01258.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.870+6242A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177451868 | ||||||
| chr2:177451908
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.870+6282C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177451908 | ||||||
| chr2:177451919
|
A | AT | 6 | a0001c0001t0002g0089a0001c0001t0011g0245a0001c0001t0011g0246others(3): Show | 6 | HG02132.hp1 HG02165.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.870+6299dupT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177451919 | |||||
| chr2:177451949
|
A | G | 12 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(9): Show | 12 | HG00735.hp1 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.870+6323A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177451949 | ||||||
| chr2:177451961
|
TA | T | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.870+6336delA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177451961 | ||||||
| chr2:177452200
|
T | C | 2 | a0001c0001t0003g0232a0001c0001t0003g0235 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.870+6574T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177452200 | ||||||
| chr2:177452314
|
T | A | 1 | a0001c0001t0001g0103 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.870+6688T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177452314 | ||||||
| chr2:177453035
|
A | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.870+7409A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177453035 | ||||||
| chr2:177453190
|
C | T | 236 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(233): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.870+7564C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177453190 | ||||||
| chr2:177453345
|
C | T | 12 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(9): Show | 12 | HG00735.hp1 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.870+7719C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177453345 | ||||||
| chr2:177453357
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.870+7731C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177453357 | ||||||
| chr2:177453533
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.870+7907A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177453533 | ||||||
| chr2:177453647
|
T | C | 108 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(105): Show | 108 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.870+8021T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177453647 | ||||||
| chr2:177453690
|
A | AT | 146 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(143): Show | 146 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.870+8086dupT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453690 | |||||
| chr2:177453690
|
A | ATT | 14 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0186others(11): Show | 14 | HG02258.hp2 HG02886.hp2 HG02922.hp1 others(11): Show |
intron_variant | MODIFIER | c.870+8085_870+8086d others(4): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453690 | |||||
| chr2:177453690
|
A | ATTT | 57 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(54): Show | 57 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.870+8084_870+8086d others(5): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453690 | |||||
| chr2:177453690
|
A | ATTTT | 12 | a0001c0001t0002g0031a0001c0001t0002g0049a0001c0001t0002g0053others(9): Show | 12 | HG00558.hp2 HG00673.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.870+8083_870+8086d others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453690 | |||||
| chr2:177453717
|
A | G | 1 | a0001c0001t0027g0226 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.870+8091A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177453717 | ||||||
| chr2:177453968
|
T | C | 1 | a0001c0001t0004g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.871-7925T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177453968 | ||||||
| chr2:177453985
|
C | CCCCCTCT others(308): Show |
1 | a0001c0001t0039g0164 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.871-7891_871-7890i others(317): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453985 | |||||
| chr2:177453985
|
C | CCCCCTCT others(312): Show |
2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.871-7891_871-7890i others(321): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453985 | |||||
| chr2:177453985
|
C | CCCCCTCT others(313): Show |
2 | a0001c0001t0001g0103a0001c0001t0001g0172 | 2 | HG02630.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.871-7891_871-7890i others(322): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453985 | |||||
| chr2:177453985
|
C | CCCCCTCT others(323): Show |
1 | a0001c0001t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.871-7891_871-7890i others(332): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453985 | |||||
| chr2:177453985
|
C | CCCCCTCT others(332): Show |
1 | a0001c0001t0001g0142 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.871-7891_871-7890i others(341): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453985 | |||||
| chr2:177453985
|
C | CCCCCTCT others(333): Show |
8 | a0001c0001t0001g0115a0001c0001t0001g0145a0001c0001t0001g0151others(5): Show | 8 | HG00609.hp1 HG02132.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.871-7891_871-7890i others(342): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453985 | |||||
| chr2:177453985
|
C | CCCCCTCT others(333): Show |
24 | a0001c0001t0001g0111a0001c0001t0001g0118a0001c0001t0001g0122others(21): Show | 24 | HG00408.hp2 HG00639.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.871-7891_871-7890i others(342): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453985 | |||||
| chr2:177453985
|
C | CCCCCTCT others(334): Show |
7 | a0001c0001t0001g0125a0001c0001t0001g0165a0001c0001t0001g0175others(4): Show | 7 | HG02074.hp1 NA18944.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.871-7891_871-7890i others(343): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453985 | |||||
| chr2:177453985
|
C | CCCCCTCT others(334): Show |
29 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(26): Show | 29 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.871-7891_871-7890i others(343): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453985 | |||||
| chr2:177453985
|
C | CCCCCTCT others(335): Show |
1 | a0001c0001t0024g0174 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.871-7891_871-7890i others(344): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453985 | |||||
| chr2:177453985
|
C | CCCCCTCT others(335): Show |
5 | a0001c0001t0001g0105a0001c0001t0001g0131a0001c0001t0001g0141others(2): Show | 5 | HG00438.hp2 HG01257.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-7891_871-7890i others(344): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453985 | |||||
| chr2:177453985
|
C | CCCCCTCT others(336): Show |
6 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0001g0101others(3): Show | 6 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.871-7891_871-7890i others(345): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453985 | |||||
| chr2:177453985
|
C | CCCCCTCT others(337): Show |
6 | a0001c0001t0001g0096a0001c0001t0001g0100a0001c0001t0001g0203others(3): Show | 6 | HG00673.hp2 HG01361.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.871-7891_871-7890i others(346): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453985 | |||||
| chr2:177453985
|
C | CCCCCTCT others(338): Show |
2 | a0001c0001t0001g0121a0001c0001t0001g0159 | 2 | HG03139.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.871-7891_871-7890i others(347): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453985 | |||||
| chr2:177453985
|
C | CCCCCTCT others(339): Show |
3 | a0001c0001t0001g0169a0001c0001t0001g0193a0001c0001t0032g0210 | 3 | NA18943.hp2 NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.871-7891_871-7890i others(348): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453985 | |||||
| chr2:177453985
|
C | CCCCCTCT others(341): Show |
2 | a0001c0001t0001g0194a0001c0001t0022g0135 | 2 | HG01256.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.871-7891_871-7890i others(350): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453985 | |||||
| chr2:177453985
|
C | CCCCCTCT others(342): Show |
1 | a0001c0001t0001g0119 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.871-7891_871-7890i others(351): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453985 | |||||
| chr2:177453985
|
C | CCCCCTCT others(344): Show |
3 | a0001c0001t0001g0110a0001c0001t0001g0120a0001c0001t0001g0144 | 3 | HG00642.hp1 HG03239.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.871-7891_871-7890i others(353): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453985 | |||||
| chr2:177453985
|
C | CCCCCTCT others(346): Show |
1 | a0001c0001t0001g0127 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.871-7891_871-7890i others(355): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177453985 | |||||
| chr2:177454078
|
T | C | 1 | a0001c0001t0042g0148 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.871-7815T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177454078 | ||||||
| chr2:177454205
|
A | G | 1 | a0001c0001t0002g0056 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.871-7688A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177454205 | ||||||
| chr2:177454240
|
G | C | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.871-7653G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177454240 | ||||||
| chr2:177454242
|
G | T | 230 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(227): Show | 230 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.871-7651G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177454242 | ||||||
| chr2:177454445
|
C | T | 1 | a0001c0001t0007g0083 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.871-7448C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177454445 | ||||||
| chr2:177454563
|
G | A | 1 | a0001c0001t0003g0233 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.871-7330G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177454563 | ||||||
| chr2:177454671
|
C | T | 1 | a0001c0001t0033g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871-7222C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177454671 | ||||||
| chr2:177454996
|
CT | C | 69 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(66): Show | 69 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.871-6886delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177454996 | |||||
| chr2:177455109
|
G | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0158 | 2 | HG02698.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.871-6784G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177455109 | ||||||
| chr2:177455490
|
C | T | 8 | a0001c0001t0001g0111a0001c0001t0001g0130a0001c0001t0001g0131others(5): Show | 8 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(5): Show |
intron_variant | MODIFIER | c.871-6403C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177455490 | ||||||
| chr2:177455494
|
A | T | 104 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(101): Show | 104 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.871-6399A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177455494 | ||||||
| chr2:177455562
|
A | G | 1 | a0001c0001t0003g0235 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.871-6331A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177455562 | ||||||
| chr2:177455604
|
A | G | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.871-6289A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177455604 | ||||||
| chr2:177455767
|
C | A | 73 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.871-6126C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177455767 | ||||||
| chr2:177455778
|
GT | G | 91 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(88): Show | 91 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.871-6104delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177455778 | |||||
| chr2:177455820
|
C | T | 12 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.871-6073C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177455820 | ||||||
| chr2:177455848
|
T | A | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.871-6045T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177455848 | ||||||
| chr2:177455885
|
C | A | 257 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(254): Show | 257 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(254): Show |
intron_variant | MODIFIER | c.871-6008C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177455885 | ||||||
| chr2:177456005
|
G | A | 3 | a0001c0001t0002g0032a0001c0001t0002g0087a0001c0001t0040g0040 | 3 | HG01074.hp1 HG02735.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.871-5888G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177456005 | ||||||
| chr2:177456220
|
T | G | 1 | a0001c0001t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.871-5673T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177456220 | ||||||
| chr2:177456279
|
G | A | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.871-5614G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177456279 | ||||||
| chr2:177456450
|
T | C | 1 | a0001c0001t0022g0135 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.871-5443T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177456450 | ||||||
| chr2:177457000
|
C | A | 1 | a0001c0001t0002g0031 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.871-4893C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177457000 | ||||||
| chr2:177457024
|
C | G | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.871-4869C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177457024 | ||||||
| chr2:177457042
|
T | G | 4 | a0001c0001t0001g0118a0001c0001t0001g0127a0001c0001t0001g0178others(1): Show | 4 | HG00639.hp2 HG01081.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-4851T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177457042 | ||||||
| chr2:177457111
|
G | A | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.871-4782G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177457111 | ||||||
| chr2:177457129
|
G | A | 91 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(88): Show | 91 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.871-4764G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177457129 | ||||||
| chr2:177457211
|
A | G | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.871-4682A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177457211 | ||||||
| chr2:177457236
|
A | G | 5 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(2): Show | 5 | HG02027.hp1 HG02132.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-4657A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177457236 | ||||||
| chr2:177457296
|
A | G | 1 | a0001c0001t0010g0170 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.871-4597A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177457296 | ||||||
| chr2:177457438
|
C | T | 136 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(133): Show | 136 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.871-4455C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177457438 | ||||||
| chr2:177457678
|
G | A | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.871-4215G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177457678 | ||||||
| chr2:177457909
|
C | T | 230 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(227): Show | 230 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.871-3984C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177457909 | ||||||
| chr2:177457924
|
C | T | 72 | a0001c0001t0001g0172a0001c0001t0002g0023a0001c0001t0002g0024others(69): Show | 72 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.871-3969C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177457924 | ||||||
| chr2:177457969
|
C | G | 1 | a0001c0001t0038g0181 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.871-3924C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177457969 | ||||||
| chr2:177458038
|
T | C | 236 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(233): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.871-3855T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177458038 | ||||||
| chr2:177458237
|
C | T | 73 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.871-3656C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177458237 | ||||||
| chr2:177458268
|
G | T | 1 | a0001c0001t0001g0141 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.871-3625G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177458268 | ||||||
| chr2:177458317
|
A | G | 8 | a0001c0001t0003g0234a0001c0001t0003g0239a0001c0001t0015g0223others(5): Show | 8 | HG00642.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.871-3576A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177458317 | ||||||
| chr2:177458344
|
A | G | 73 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.871-3549A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177458344 | ||||||
| chr2:177458363
|
T | G | 2 | a0001c0001t0007g0034a0001c0001t0007g0064 | 2 | NA18946.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.871-3530T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177458363 | ||||||
| chr2:177458406
|
G | C | 2 | a0001c0001t0033g0195a0001c0001t0035g0017 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.871-3487G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177458406 | ||||||
| chr2:177458425
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.871-3468G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177458425 | ||||||
| chr2:177458446
|
G | A | 1 | a0001c0001t0003g0231 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.871-3447G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177458446 | ||||||
| chr2:177458477
|
G | A | 15 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(12): Show | 15 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(12): Show |
intron_variant | MODIFIER | c.871-3416G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177458477 | ||||||
| chr2:177458527
|
A | G | 2 | a0001c0001t0025g0253a0001c0001t0025g0254 | 2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.871-3366A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177458527 | ||||||
| chr2:177458859
|
G | A | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.871-3034G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177458859 | ||||||
| chr2:177458920
|
A | G | 73 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.871-2973A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177458920 | ||||||
| chr2:177458990
|
G | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0013g0188 | 3 | NA18939.hp1 NA18985.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.871-2903G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177458990 | ||||||
| chr2:177459038
|
A | G | 7 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(4): Show | 7 | HG00735.hp1 HG01891.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.871-2855A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177459038 | ||||||
| chr2:177459082
|
A | G | 134 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(131): Show | 134 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.871-2811A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177459082 | ||||||
| chr2:177459152
|
C | T | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.871-2741C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177459152 | ||||||
| chr2:177459159
|
A | C | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.871-2734A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177459159 | ||||||
| chr2:177459168
|
A | C | 1 | a0001c0001t0051g0228 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.871-2725A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177459168 | ||||||
| chr2:177459271
|
C | A | 2 | a0001c0001t0002g0053a0001c0001t0002g0249 | 2 | HG02074.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.871-2622C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177459271 | ||||||
| chr2:177459369
|
T | C | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.871-2524T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177459369 | ||||||
| chr2:177459569
|
G | C | 1 | a0001c0001t0001g0203 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.871-2324G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177459569 | ||||||
| chr2:177459629
|
C | T | 17 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(14): Show | 17 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(14): Show |
intron_variant | MODIFIER | c.871-2264C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177459629 | ||||||
| chr2:177459701
|
C | A | 2 | a0001c0001t0003g0241a0001c0001t0003g0242 | 2 | HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.871-2192C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177459701 | ||||||
| chr2:177460151
|
A | C | 92 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(89): Show | 92 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.871-1742A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177460151 | ||||||
| chr2:177460165
|
C | T | 1 | a0001c0001t0020g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.871-1728C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177460165 | ||||||
| chr2:177460180
|
G | C | 1 | a0001c0001t0001g0103 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.871-1713G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177460180 | ||||||
| chr2:177460317
|
T | TA | 12 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.871-1567dupA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177460317 | |||||
| chr2:177460747
|
C | T | 8 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(5): Show | 8 | HG00408.hp1 HG00438.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.871-1146C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177460747 | ||||||
| chr2:177460850
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.871-1043C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177460850 | ||||||
| chr2:177461032
|
T | C | 1 | a0001c0001t0020g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.871-861T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177461032 | ||||||
| chr2:177461309
|
T | C | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.871-584T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177461309 | ||||||
| chr2:177461714
|
A | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0159 | 2 | HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.871-179A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177461714 | ||||||
| chr2:177461742
|
A | G | 12 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.871-151A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | chr2 | 177461742 | ||||||
| chr2:177461748
|
C | CT | 12 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0001g0106others(9): Show | 12 | HG00642.hp1 HG01257.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.871-129dupT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177461748 | |||||
| chr2:177461748
|
CT | C | 77 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(74): Show | 77 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.871-129delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 177461748 | |||||
| chr2:177462074
|
A | G | 1 | a0001c0001t0010g0205 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.996+56A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177462074 | ||||||
| chr2:177462110
|
C | G | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.996+92C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177462110 | ||||||
| chr2:177462119
|
G | A | 113 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(110): Show | 113 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.996+101G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177462119 | ||||||
| chr2:177462166
|
G | A | 5 | a0001c0001t0025g0253a0001c0001t0025g0254a0001c0003t0001g0255others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.996+148G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177462166 | ||||||
| chr2:177462224
|
A | G | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.996+206A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177462224 | ||||||
| chr2:177462275
|
C | T | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.996+257C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177462275 | ||||||
| chr2:177462392
|
C | CA | 187 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(184): Show | 187 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.996+387dupA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr2 | 177462392 | |||||
| chr2:177462392
|
C | CAA | 18 | a0001c0001t0001g0131a0001c0001t0001g0167a0001c0001t0001g0186others(15): Show | 18 | HG02109.hp1 HG02258.hp2 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.996+386_996+387dup others(2): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr2 | 177462392 | |||||
| chr2:177462406
|
G | A | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.996+388G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177462406 | ||||||
| chr2:177462409
|
A | G | 2 | a0001c0001t0033g0195a0001c0001t0035g0017 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.996+391A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177462409 | ||||||
| chr2:177462552
|
C | T | 1 | a0001c0001t0005g0201 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.996+534C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177462552 | ||||||
| chr2:177462831
|
G | A | 4 | a0001c0001t0001g0142a0001c0001t0001g0153a0001c0001t0001g0184others(1): Show | 4 | HG01255.hp2 HG01928.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.996+813G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177462831 | ||||||
| chr2:177462999
|
C | T | 133 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(130): Show | 133 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.996+981C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177462999 | ||||||
| chr2:177463050
|
T | G | 2 | a0001c0001t0021g0027a0001c0001t0021g0028 | 2 | HG00438.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.996+1032T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177463050 | ||||||
| chr2:177463147
|
C | T | 2 | a0001c0001t0003g0241a0001c0001t0003g0242 | 2 | HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.996+1129C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177463147 | ||||||
| chr2:177463263
|
C | T | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.996+1245C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177463263 | ||||||
| chr2:177463311
|
T | C | 6 | a0001c0001t0006g0043a0001c0001t0006g0045a0001c0001t0006g0047others(3): Show | 6 | HG00544.hp1 HG00597.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.996+1293T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177463311 | ||||||
| chr2:177463373
|
G | A | 73 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.996+1355G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177463373 | ||||||
| chr2:177463462
|
G | A | 5 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0001g0185others(2): Show | 5 | HG00673.hp2 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.996+1444G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177463462 | ||||||
| chr2:177463709
|
A | G | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.996+1691A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177463709 | ||||||
| chr2:177463971
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.996+1953C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177463971 | ||||||
| chr2:177464027
|
C | T | 1 | a0001c0001t0003g0231 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.996+2009C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177464027 | ||||||
| chr2:177464680
|
C | T | 5 | a0001c0001t0012g0014a0001c0001t0012g0015a0001c0001t0012g0016others(2): Show | 5 | HG02258.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.996+2662C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177464680 | ||||||
| chr2:177464724
|
T | TA | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.996+2707dupA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr2 | 177464724 | |||||
| chr2:177464752
|
G | A | 1 | a0001c0001t0035g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.996+2734G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177464752 | ||||||
| chr2:177465207
|
C | T | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.996+3189C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177465207 | ||||||
| chr2:177465289
|
A | AT | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.997-3117dupT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr2 | 177465289 | |||||
| chr2:177465338
|
AC | A | 134 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(131): Show | 134 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.997-3077delC | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177465338 | ||||||
| chr2:177465445
|
C | G | 134 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(131): Show | 134 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.997-2971C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177465445 | ||||||
| chr2:177465655
|
T | C | 5 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(2): Show | 5 | HG02027.hp1 HG02132.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.997-2761T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177465655 | ||||||
| chr2:177465876
|
T | C | 236 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(233): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.997-2540T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177465876 | ||||||
| chr2:177465925
|
C | T | 1 | a0001c0001t0019g0114 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.997-2491C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177465925 | ||||||
| chr2:177466038
|
A | G | 2 | a0001c0001t0001g0125a0001c0001t0001g0151 | 2 | NA19065.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.997-2378A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177466038 | ||||||
| chr2:177466075
|
A | T | 2 | a0001c0002t0009g0204a0001c0002t0034g0211 | 2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.997-2341A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177466075 | ||||||
| chr2:177466450
|
G | C | 1 | a0001c0001t0003g0233 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.997-1966G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177466450 | ||||||
| chr2:177466478
|
G | A | 137 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(134): Show | 137 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.997-1938G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177466478 | ||||||
| chr2:177466614
|
T | G | 6 | a0001c0001t0012g0014a0001c0001t0012g0015a0001c0001t0012g0016others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.997-1802T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177466614 | ||||||
| chr2:177466666
|
C | T | 1 | a0001c0001t0012g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.997-1750C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177466666 | ||||||
| chr2:177466685
|
C | T | 5 | a0001c0001t0025g0253a0001c0001t0025g0254a0001c0003t0001g0255others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.997-1731C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177466685 | ||||||
| chr2:177466758
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.997-1658A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177466758 | ||||||
| chr2:177466911
|
C | T | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.997-1505C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177466911 | ||||||
| chr2:177466939
|
A | G | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.997-1477A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177466939 | ||||||
| chr2:177466955
|
G | A | 1 | a0001c0001t0006g0048 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.997-1461G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177466955 | ||||||
| chr2:177467081
|
CACTGCAG others(31): Show |
C | 6 | a0001c0001t0012g0014a0001c0001t0012g0015a0001c0001t0012g0016others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.997-1334_997-1297d others(40): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177467081 | ||||||
| chr2:177467330
|
C | A | 1 | a0001c0001t0003g0237 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.997-1086C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177467330 | ||||||
| chr2:177467574
|
A | T | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.997-842A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177467574 | ||||||
| chr2:177467577
|
T | C | 8 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(5): Show | 8 | HG00408.hp1 HG00438.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.997-839T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177467577 | ||||||
| chr2:177467595
|
T | C | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.997-821T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177467595 | ||||||
| chr2:177467648
|
T | C | 1 | a0001c0001t0001g0167 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.997-768T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177467648 | ||||||
| chr2:177467694
|
C | G | 1 | a0001c0001t0010g0205 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.997-722C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177467694 | ||||||
| chr2:177467775
|
C | T | 4 | a0001c0001t0001g0154a0001c0001t0001g0157a0001c0001t0001g0160others(1): Show | 4 | NA18951.hp2 NA18999.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.997-641C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177467775 | ||||||
| chr2:177467928
|
G | A | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.997-488G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 9/19 | chr2 | 177467928 | ||||||
| chr2:177468863
|
G | A | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1105+339G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177468863 | ||||||
| chr2:177468963
|
G | A | 1 | a0001c0001t0020g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1105+439G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177468963 | ||||||
| chr2:177469017
|
G | A | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1105+493G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177469017 | ||||||
| chr2:177469070
|
G | A | 2 | a0001c0001t0021g0027a0001c0001t0021g0028 | 2 | HG00438.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1105+546G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177469070 | ||||||
| chr2:177469179
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1105+655A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177469179 | ||||||
| chr2:177469227
|
A | G | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1105+703A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177469227 | ||||||
| chr2:177469348
|
C | T | 1 | a0001c0001t0008g0218 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1105+824C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177469348 | ||||||
| chr2:177469634
|
GTTAC | G | 5 | a0001c0001t0016g0212a0001c0001t0016g0213a0001c0001t0016g0214others(2): Show | 5 | HG02055.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1105+1114_1105+111 others(8): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr2 | 177469634 | |||||
| chr2:177470051
|
T | C | 1 | a0001c0001t0009g0091 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1105+1527T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177470051 | ||||||
| chr2:177470156
|
T | C | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1105+1632T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177470156 | ||||||
| chr2:177470306
|
G | T | 70 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(67): Show | 70 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1105+1782G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177470306 | ||||||
| chr2:177470397
|
G | A | 3 | a0001c0003t0001g0255a0001c0003t0005g0256a0001c0003t0005g0257 | 3 | HG02258.hp1 HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1105+1873G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177470397 | ||||||
| chr2:177470448
|
A | C | 21 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(18): Show | 21 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1105+1924A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177470448 | ||||||
| chr2:177470628
|
C | T | 73 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1105+2104C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177470628 | ||||||
| chr2:177470710
|
C | CA | 117 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0001g0106others(114): Show | 117 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.1105+2201dupA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr2 | 177470710 | |||||
| chr2:177470710
|
C | CAAA | 6 | a0001c0001t0005g0197a0001c0001t0005g0199a0001c0001t0005g0200others(3): Show | 6 | HG00735.hp1 HG01891.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1105+2199_1105+220 others(7): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr2 | 177470710 | |||||
| chr2:177470714
|
AAAAAAAA others(5): Show |
A | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1105+2201_1105+221 others(16): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr2 | 177470714 | |||||
| chr2:177470726
|
G | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0185 | 2 | HG04199.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1105+2202G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177470726 | ||||||
| chr2:177470727
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1105+2203A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177470727 | ||||||
| chr2:177470741
|
T | A | 5 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(2): Show | 5 | HG02027.hp1 HG02132.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1105+2217T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177470741 | ||||||
| chr2:177470758
|
T | A | 230 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(227): Show | 230 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.1105+2234T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177470758 | ||||||
| chr2:177470811
|
A | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1105+2287A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177470811 | ||||||
| chr2:177470925
|
T | C | 15 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(12): Show | 15 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(12): Show |
intron_variant | MODIFIER | c.1105+2401T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177470925 | ||||||
| chr2:177470928
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1105+2404C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177470928 | ||||||
| chr2:177470968
|
G | A | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.1105+2444G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177470968 | ||||||
| chr2:177471109
|
T | C | 5 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(2): Show | 5 | HG02027.hp1 HG02132.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1105+2585T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177471109 | ||||||
| chr2:177471354
|
G | A | 1 | a0001c0001t0005g0200 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1105+2830G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177471354 | ||||||
| chr2:177471429
|
A | G | 4 | a0001c0001t0015g0223a0001c0001t0015g0224a0001c0001t0015g0225others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.1105+2905A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177471429 | ||||||
| chr2:177471478
|
G | A | 2 | a0001c0002t0009g0204a0001c0002t0034g0211 | 2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1105+2954G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177471478 | ||||||
| chr2:177471493
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1105+2969G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177471493 | ||||||
| chr2:177471923
|
C | T | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1105+3399C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177471923 | ||||||
| chr2:177471931
|
C | A | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1105+3407C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177471931 | ||||||
| chr2:177472012
|
T | A | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1105+3488T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177472012 | ||||||
| chr2:177472036
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1105+3512G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177472036 | ||||||
| chr2:177472081
|
G | A | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.1105+3557G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177472081 | ||||||
| chr2:177472150
|
A | G | 137 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(134): Show | 137 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.1105+3626A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177472150 | ||||||
| chr2:177472218
|
C | T | 70 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(67): Show | 70 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1105+3694C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177472218 | ||||||
| chr2:177472303
|
G | A | 113 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(110): Show | 113 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1105+3779G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177472303 | ||||||
| chr2:177472361
|
C | A | 92 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(89): Show | 92 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1105+3837C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177472361 | ||||||
| chr2:177472521
|
G | A | 70 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(67): Show | 70 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1105+3997G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177472521 | ||||||
| chr2:177472575
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1105+4051G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177472575 | ||||||
| chr2:177472668
|
G | A | 70 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(67): Show | 70 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1105+4144G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177472668 | ||||||
| chr2:177472702
|
C | T | 1 | a0001c0001t0025g0253 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1105+4178C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177472702 | ||||||
| chr2:177472984
|
T | C | 7 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(4): Show | 7 | HG01109.hp1 HG01243.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1105+4460T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177472984 | ||||||
| chr2:177473153
|
C | T | 3 | a0001c0001t0012g0014a0001c0001t0012g0015a0001c0001t0012g0016 | 3 | HG02258.hp2 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1105+4629C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177473153 | ||||||
| chr2:177473215
|
T | C | 3 | a0001c0001t0001g0165a0001c0001t0001g0175a0001c0001t0001g0187 | 3 | NA18946.hp2 NA18947.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1105+4691T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177473215 | ||||||
| chr2:177473252
|
G | T | 2 | a0001c0001t0017g0207a0001c0001t0017g0208 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1105+4728G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177473252 | ||||||
| chr2:177473434
|
G | A | 247 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(244): Show | 247 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.1105+4910G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177473434 | ||||||
| chr2:177473817
|
T | C | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1105+5293T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177473817 | ||||||
| chr2:177473939
|
A | T | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1105+5415A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177473939 | ||||||
| chr2:177474014
|
C | T | 1 | a0001c0001t0002g0057 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1105+5490C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177474014 | ||||||
| chr2:177474026
|
A | G | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1105+5502A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177474026 | ||||||
| chr2:177474102
|
A | T | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1105+5578A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177474102 | ||||||
| chr2:177474212
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1105+5688C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177474212 | ||||||
| chr2:177474503
|
C | T | 2 | a0001c0002t0009g0204a0001c0002t0034g0211 | 2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1105+5979C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177474503 | ||||||
| chr2:177474559
|
C | T | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1105+6035C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177474559 | ||||||
| chr2:177474634
|
A | G | 2 | a0001c0001t0023g0074a0001c0001t0023g0075 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1105+6110A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177474634 | ||||||
| chr2:177474702
|
G | A | 5 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(2): Show | 5 | HG02132.hp1 HG02165.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1105+6178G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177474702 | ||||||
| chr2:177474708
|
A | G | 1 | a0001c0001t0004g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1105+6184A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177474708 | ||||||
| chr2:177474732
|
G | A | 1 | a0001c0002t0034g0211 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1105+6208G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177474732 | ||||||
| chr2:177474804
|
C | T | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1105+6280C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177474804 | ||||||
| chr2:177474805
|
C | A | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1105+6281C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177474805 | ||||||
| chr2:177475001
|
C | T | 1 | a0001c0001t0037g0019 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1105+6477C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177475001 | ||||||
| chr2:177475042
|
C | G | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1105+6518C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177475042 | ||||||
| chr2:177475079
|
A | T | 2 | a0001c0001t0021g0027a0001c0001t0021g0028 | 2 | HG00438.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1105+6555A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177475079 | ||||||
| chr2:177475129
|
A | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1105+6605A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177475129 | ||||||
| chr2:177475150
|
C | G | 2 | a0001c0001t0023g0074a0001c0001t0023g0075 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1105+6626C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177475150 | ||||||
| chr2:177475337
|
TA | T | 7 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(4): Show | 7 | HG02132.hp1 HG02165.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1106-6721delA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177475337 | ||||||
| chr2:177475792
|
T | G | 91 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(88): Show | 91 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1106-6267T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177475792 | ||||||
| chr2:177475984
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1106-6075A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177475984 | ||||||
| chr2:177476038
|
G | C | 136 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(133): Show | 136 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1106-6021G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177476038 | ||||||
| chr2:177476525
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1106-5534A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177476525 | ||||||
| chr2:177476530
|
T | C | 1 | a0001c0001t0039g0164 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1106-5529T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177476530 | ||||||
| chr2:177476560
|
CAA | C | 7 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(4): Show | 7 | HG00735.hp1 HG01891.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1106-5498_1106-549 others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177476560 | ||||||
| chr2:177476770
|
T | C | 10 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0066others(7): Show | 10 | HG03831.hp2 NA18943.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.1106-5289T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177476770 | ||||||
| chr2:177476785
|
A | T | 1 | a0001c0001t0002g0026 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1106-5274A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177476785 | ||||||
| chr2:177476960
|
G | A | 236 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(233): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1106-5099G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177476960 | ||||||
| chr2:177477131
|
C | G | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106-4928C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177477131 | ||||||
| chr2:177477180
|
T | C | 5 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(2): Show | 5 | HG02027.hp1 HG02132.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1106-4879T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177477180 | ||||||
| chr2:177477268
|
G | A | 5 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0001g0185others(2): Show | 5 | HG00673.hp2 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1106-4791G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177477268 | ||||||
| chr2:177477460
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1106-4599A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177477460 | ||||||
| chr2:177477517
|
C | T | 6 | a0001c0001t0012g0014a0001c0001t0012g0015a0001c0001t0012g0016others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1106-4542C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177477517 | ||||||
| chr2:177477595
|
A | T | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106-4464A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177477595 | ||||||
| chr2:177477618
|
C | T | 17 | a0001c0001t0004g0093a0001c0001t0017g0207a0001c0001t0017g0208others(14): Show | 17 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(14): Show |
intron_variant | MODIFIER | c.1106-4441C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177477618 | ||||||
| chr2:177477619
|
A | G | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.1106-4440A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177477619 | ||||||
| chr2:177477629
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1106-4430A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177477629 | ||||||
| chr2:177477857
|
A | T | 9 | a0001c0001t0001g0111a0001c0001t0001g0130a0001c0001t0001g0131others(6): Show | 9 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(6): Show |
intron_variant | MODIFIER | c.1106-4202A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177477857 | ||||||
| chr2:177477869
|
A | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1106-4190A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177477869 | ||||||
| chr2:177477893
|
G | C | 1 | a0001c0001t0010g0147 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1106-4166G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177477893 | ||||||
| chr2:177477935
|
G | A | 2 | a0001c0001t0025g0253a0001c0001t0025g0254 | 2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1106-4124G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177477935 | ||||||
| chr2:177477948
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1106-4111T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177477948 | ||||||
| chr2:177477981
|
A | G | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106-4078A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177477981 | ||||||
| chr2:177478004
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1106-4055G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177478004 | ||||||
| chr2:177478044
|
A | G | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1106-4015A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177478044 | ||||||
| chr2:177478064
|
TATCTGGG | T | 3 | a0001c0001t0001g0096a0001c0001t0001g0100a0001c0001t0041g0099 | 3 | HG01361.hp1 HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1106-3993_1106-398 others(11): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr2 | 177478064 | |||||
| chr2:177478127
|
G | T | 1 | a0001c0001t0010g0123 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1106-3932G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177478127 | ||||||
| chr2:177478407
|
A | C | 1 | a0001c0001t0002g0090 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1106-3652A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177478407 | ||||||
| chr2:177478407
|
A | G | 1 | a0001c0001t0003g0234 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1106-3652A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177478407 | ||||||
| chr2:177478481
|
C | T | 5 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(2): Show | 5 | HG02027.hp1 HG02132.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1106-3578C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177478481 | ||||||
| chr2:177478610
|
C | T | 3 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254 | 3 | HG03195.hp2 HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1106-3449C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177478610 | ||||||
| chr2:177478665
|
A | G | 71 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(68): Show | 71 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1106-3394A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177478665 | ||||||
| chr2:177478776
|
T | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0158 | 2 | HG02698.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1106-3283T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177478776 | ||||||
| chr2:177478782
|
A | T | 3 | a0001c0001t0002g0050a0001c0001t0002g0057a0001c0001t0002g0062 | 3 | NA18964.hp1 NA18968.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1106-3277A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177478782 | ||||||
| chr2:177478818
|
G | A | 6 | a0001c0001t0012g0014a0001c0001t0012g0015a0001c0001t0012g0016others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1106-3241G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177478818 | ||||||
| chr2:177478903
|
C | A | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1106-3156C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177478903 | ||||||
| chr2:177479030
|
T | A | 1 | a0001c0001t0033g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1106-3029T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177479030 | ||||||
| chr2:177479148
|
G | A | 2 | a0001c0001t0003g0232a0001c0001t0003g0235 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1106-2911G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177479148 | ||||||
| chr2:177479227
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1106-2832G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177479227 | ||||||
| chr2:177479481
|
T | C | 5 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(2): Show | 5 | HG02027.hp1 HG02132.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1106-2578T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177479481 | ||||||
| chr2:177479750
|
T | C | 5 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(2): Show | 5 | HG02027.hp1 HG02132.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1106-2309T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177479750 | ||||||
| chr2:177479771
|
G | A | 7 | a0001c0001t0001g0118a0001c0001t0001g0127a0001c0001t0001g0178others(4): Show | 7 | HG00639.hp2 HG01081.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1106-2288G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177479771 | ||||||
| chr2:177479792
|
G | T | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106-2267G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177479792 | ||||||
| chr2:177479794
|
T | C | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1106-2265T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177479794 | ||||||
| chr2:177479798
|
T | C | 1 | a0001c0001t0004g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1106-2261T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177479798 | ||||||
| chr2:177480049
|
G | A | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106-2010G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177480049 | ||||||
| chr2:177480189
|
T | A | 232 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(229): Show | 232 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.1106-1870T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177480189 | ||||||
| chr2:177480426
|
A | G | 15 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(12): Show | 15 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1106-1633A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177480426 | ||||||
| chr2:177480445
|
G | T | 1 | a0001c0001t0006g0047 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1106-1614G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177480445 | ||||||
| chr2:177480459
|
C | T | 1 | a0001c0001t0006g0047 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1106-1600C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177480459 | ||||||
| chr2:177480566
|
T | C | 230 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(227): Show | 230 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.1106-1493T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177480566 | ||||||
| chr2:177480581
|
C | T | 133 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(130): Show | 133 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.1106-1478C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177480581 | ||||||
| chr2:177480609
|
G | A | 15 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(12): Show | 15 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1106-1450G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177480609 | ||||||
| chr2:177480618
|
C | A | 15 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(12): Show | 15 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1106-1441C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177480618 | ||||||
| chr2:177480854
|
G | A | 1 | a0001c0001t0002g0081 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1106-1205G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177480854 | ||||||
| chr2:177480919
|
C | T | 1 | a0001c0001t0009g0091 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1106-1140C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177480919 | ||||||
| chr2:177480921
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1106-1138A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177480921 | ||||||
| chr2:177481124
|
C | T | 3 | a0001c0001t0001g0171a0001c0001t0017g0207a0001c0001t0017g0208 | 3 | HG01074.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1106-935C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177481124 | ||||||
| chr2:177481145
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1106-914G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177481145 | ||||||
| chr2:177481280
|
C | T | 1 | a0001c0001t0013g0188 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1106-779C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177481280 | ||||||
| chr2:177481460
|
G | A | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106-599G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177481460 | ||||||
| chr2:177481638
|
G | GT | 4 | a0001c0001t0002g0072a0001c0001t0002g0078a0001c0001t0005g0104others(1): Show | 4 | HG02027.hp1 HG02486.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106-414dupT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr2 | 177481638 | |||||
| chr2:177481846
|
T | G | 24 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231others(21): Show | 24 | HG00642.hp2 HG01167.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.1106-213T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177481846 | ||||||
| chr2:177481926
|
GCCATTAT others(3): Show |
G | 94 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(91): Show | 94 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1106-129_1106-120d others(12): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr2 | 177481926 | |||||
| chr2:177481964
|
G | C | 1 | a0001c0001t0010g0147 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1106-95G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 10/19 | chr2 | 177481964 | ||||||
| chr2:177482200
|
T | A | 1 | a0001c0001t0032g0210 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1233+14T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177482200 | ||||||
| chr2:177482847
|
A | T | 19 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231others(16): Show | 19 | HG00642.hp2 HG01167.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1233+661A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177482847 | ||||||
| chr2:177482853
|
G | A | 3 | a0001c0001t0011g0246a0001c0001t0011g0247a0001c0001t0011g0248 | 3 | HG02165.hp1 NA18999.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1233+667G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177482853 | ||||||
| chr2:177482861
|
T | A | 6 | a0001c0001t0012g0014a0001c0001t0012g0015a0001c0001t0012g0016others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1233+675T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177482861 | ||||||
| chr2:177482931
|
TC | T | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1233+748delC | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177482931 | |||||
| chr2:177482966
|
G | A | 4 | a0001c0001t0015g0223a0001c0001t0015g0224a0001c0001t0015g0225others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+780G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177482966 | ||||||
| chr2:177483075
|
T | C | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1233+889T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177483075 | ||||||
| chr2:177483324
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1233+1138A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177483324 | ||||||
| chr2:177483394
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1233+1208T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177483394 | ||||||
| chr2:177483716
|
A | T | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.1233+1530A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177483716 | ||||||
| chr2:177483724
|
T | A | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1233+1538T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177483724 | ||||||
| chr2:177483892
|
A | G | 71 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(68): Show | 71 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1233+1706A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177483892 | ||||||
| chr2:177484010
|
GT | G | 149 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(146): Show | 149 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.1233+1839delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177484010 | |||||
| chr2:177484010
|
GTT | G | 86 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(83): Show | 86 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1233+1838_1233+183 others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177484010 | |||||
| chr2:177484230
|
G | A | 1 | a0001c0001t0002g0086 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1233+2044G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177484230 | ||||||
| chr2:177484338
|
G | C | 76 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(73): Show | 76 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.1233+2152G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177484338 | ||||||
| chr2:177484367
|
G | A | 2 | a0001c0002t0004g0004a0001c0002t0004g0007 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1233+2181G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177484367 | ||||||
| chr2:177484638
|
G | T | 1 | a0001c0001t0001g0189 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1233+2452G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177484638 | ||||||
| chr2:177485426
|
G | A | 7 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(4): Show | 7 | HG00735.hp1 HG01891.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1233+3240G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177485426 | ||||||
| chr2:177485456
|
C | T | 1 | a0001c0001t0042g0148 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1233+3270C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177485456 | ||||||
| chr2:177485501
|
A | G | 1 | a0001c0001t0020g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1233+3315A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177485501 | ||||||
| chr2:177485645
|
G | A | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1233+3459G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177485645 | ||||||
| chr2:177485887
|
A | C | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1233+3701A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177485887 | ||||||
| chr2:177485959
|
A | G | 1 | a0001c0001t0043g0143 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1233+3773A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177485959 | ||||||
| chr2:177486015
|
C | T | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1233+3829C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177486015 | ||||||
| chr2:177486186
|
A | G | 2 | a0001c0002t0009g0204a0001c0002t0034g0211 | 2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1233+4000A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177486186 | ||||||
| chr2:177486303
|
G | A | 1 | a0001c0001t0046g0209 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1233+4117G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177486303 | ||||||
| chr2:177486425
|
A | T | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1233+4239A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177486425 | ||||||
| chr2:177486726
|
G | GCTATATG others(335): Show |
2 | a0001c0001t0001g0112a0001c0001t0001g0122 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1233+4552_1233+455 others(346): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(338): Show |
1 | a0001c0001t0010g0170 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1233+4552_1233+455 others(349): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(359): Show |
1 | a0001c0001t0037g0019 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1233+4552_1233+455 others(370): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(335): Show |
1 | a0001c0001t0001g0116 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1233+4552_1233+455 others(346): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(336): Show |
5 | a0001c0001t0001g0110a0001c0001t0001g0133a0001c0001t0001g0136others(2): Show | 5 | HG00544.hp2 HG00642.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233+4552_1233+455 others(347): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(337): Show |
9 | a0001c0001t0001g0108a0001c0001t0001g0120a0001c0001t0001g0129others(6): Show | 9 | HG00558.hp1 HG00639.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.1233+4552_1233+455 others(348): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(338): Show |
3 | a0001c0001t0001g0095a0001c0001t0001g0168a0001c0001t0001g0175 | 3 | HG02559.hp2 NA18947.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.1233+4552_1233+455 others(349): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(340): Show |
2 | a0001c0001t0001g0169a0001c0001t0001g0193 | 2 | NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1233+4552_1233+455 others(351): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(324): Show |
1 | a0001c0001t0001g0190 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1233+4552_1233+455 others(335): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(335): Show |
6 | a0001c0001t0001g0128a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 6 | HG00438.hp2 HG00738.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.1233+4552_1233+455 others(346): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(336): Show |
40 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(37): Show | 40 | HG00597.hp1 HG00609.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.1233+4552_1233+455 others(347): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(337): Show |
15 | a0001c0001t0001g0094a0001c0001t0001g0119a0001c0001t0001g0121others(12): Show | 15 | HG00408.hp2 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.1233+4552_1233+455 others(348): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(338): Show |
3 | a0001c0001t0001g0156a0001c0001t0001g0172a0001c0001t0009g0162 | 3 | HG03927.hp1 HG04184.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1233+4552_1233+455 others(349): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(339): Show |
3 | a0001c0001t0001g0111a0001c0001t0001g0130a0001c0001t0001g0132 | 3 | HG00423.hp2 NA18966.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1233+4552_1233+455 others(350): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(339): Show |
2 | a0001c0002t0009g0204a0001c0002t0034g0211 | 2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1233+4552_1233+455 others(350): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(340): Show |
3 | a0001c0001t0001g0131a0001c0001t0001g0194a0001c0001t0038g0181 | 3 | HG01256.hp1 HG02027.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1233+4552_1233+455 others(351): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(334): Show |
1 | a0001c0001t0013g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1233+4552_1233+455 others(345): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(335): Show |
3 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0001g0100 | 3 | HG01884.hp2 HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1233+4552_1233+455 others(346): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(336): Show |
6 | a0001c0001t0001g0096a0001c0001t0001g0101a0001c0001t0001g0102others(3): Show | 6 | HG01361.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1233+4552_1233+455 others(347): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(337): Show |
1 | a0001c0002t0013g0206 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1233+4552_1233+455 others(348): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(337): Show |
1 | a0001c0001t0001g0103 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1233+4552_1233+455 others(348): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(338): Show |
1 | a0001c0001t0001g0203 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1233+4552_1233+455 others(349): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486726
|
G | GCTATATG others(328): Show |
3 | a0001c0001t0012g0014a0001c0001t0012g0015a0001c0001t0012g0016 | 3 | HG02258.hp2 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1233+4552_1233+455 others(339): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177486726 | |||||
| chr2:177486819
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1233+4633C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177486819 | ||||||
| chr2:177486830
|
C | T | 1 | a0001c0001t0022g0134 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1233+4644C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177486830 | ||||||
| chr2:177486839
|
C | G | 236 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(233): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1233+4653C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177486839 | ||||||
| chr2:177486877
|
G | A | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.1233+4691G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177486877 | ||||||
| chr2:177487102
|
T | G | 1 | a0001c0001t0001g0178 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1233+4916T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177487102 | ||||||
| chr2:177487362
|
A | G | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1233+5176A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177487362 | ||||||
| chr2:177487399
|
T | C | 236 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(233): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1233+5213T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177487399 | ||||||
| chr2:177487463
|
T | A | 70 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(67): Show | 70 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1233+5277T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177487463 | ||||||
| chr2:177487519
|
A | C | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1233+5333A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177487519 | ||||||
| chr2:177487611
|
C | A | 1 | a0001c0001t0001g0203 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1233+5425C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177487611 | ||||||
| chr2:177487623
|
C | A | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1233+5437C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177487623 | ||||||
| chr2:177487699
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0029g0166 | 2 | HG00639.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1234-5449G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177487699 | ||||||
| chr2:177487734
|
C | A | 5 | a0001c0001t0007g0034a0001c0001t0007g0064a0001c0001t0007g0065others(2): Show | 5 | HG00558.hp2 HG00673.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234-5414C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177487734 | ||||||
| chr2:177487956
|
A | G | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.1234-5192A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177487956 | ||||||
| chr2:177487971
|
G | A | 1 | a0001c0001t0013g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1234-5177G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177487971 | ||||||
| chr2:177488018
|
G | A | 134 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(131): Show | 134 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.1234-5130G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177488018 | ||||||
| chr2:177488370
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1234-4778G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177488370 | ||||||
| chr2:177488611
|
G | T | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1234-4537G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177488611 | ||||||
| chr2:177488654
|
A | G | 71 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(68): Show | 71 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1234-4494A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177488654 | ||||||
| chr2:177488928
|
A | G | 1 | a0001c0001t0020g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1234-4220A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177488928 | ||||||
| chr2:177489087
|
C | CT | 139 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(136): Show | 139 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.1234-4046dupT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177489087 | |||||
| chr2:177489227
|
G | A | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1234-3921G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177489227 | ||||||
| chr2:177489279
|
T | G | 1 | a0001c0001t0035g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1234-3869T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177489279 | ||||||
| chr2:177489306
|
G | A | 1 | a0001c0001t0002g0035 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1234-3842G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177489306 | ||||||
| chr2:177489444
|
C | T | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.1234-3704C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177489444 | ||||||
| chr2:177489583
|
G | A | 5 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(2): Show | 5 | HG00735.hp1 HG01891.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1234-3565G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177489583 | ||||||
| chr2:177489627
|
G | A | 1 | a0001c0001t0003g0239 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1234-3521G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177489627 | ||||||
| chr2:177489629
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1234-3519A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177489629 | ||||||
| chr2:177490096
|
C | T | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1234-3052C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177490096 | ||||||
| chr2:177490319
|
A | G | 1 | a0001c0002t0004g0004 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1234-2829A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177490319 | ||||||
| chr2:177490378
|
T | C | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1234-2770T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177490378 | ||||||
| chr2:177490623
|
A | T | 2 | a0001c0001t0002g0089a0001c0001t0045g0038 | 2 | NA18949.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1234-2525A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177490623 | ||||||
| chr2:177490685
|
C | T | 1 | a0001c0001t0013g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1234-2463C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177490685 | ||||||
| chr2:177490806
|
G | T | 73 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1234-2342G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177490806 | ||||||
| chr2:177490846
|
C | CT | 25 | a0001c0001t0001g0122a0001c0001t0001g0137a0001c0001t0001g0142others(22): Show | 25 | HG00639.hp2 HG01169.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.1234-2277dupT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177490846 | |||||
| chr2:177490846
|
C | CTT | 109 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(106): Show | 109 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1234-2278_1234-227 others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177490846 | |||||
| chr2:177490846
|
C | CTTT | 12 | a0001c0001t0001g0125a0001c0001t0001g0145a0001c0001t0001g0163others(9): Show | 12 | HG00609.hp1 HG01243.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.1234-2279_1234-227 others(7): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177490846 | |||||
| chr2:177490846
|
CT | C | 5 | a0001c0001t0002g0068a0001c0001t0003g0230a0001c0001t0003g0243others(2): Show | 5 | HG01167.hp2 HG03225.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234-2277delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177490846 | |||||
| chr2:177490854
|
T | TTTG | 7 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(4): Show | 7 | HG00735.hp1 HG01891.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1234-2292_1234-229 others(7): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177490854 | |||||
| chr2:177490858
|
T | G | 7 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(4): Show | 7 | HG00735.hp1 HG01891.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1234-2290T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177490858 | ||||||
| chr2:177490862
|
T | G | 7 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(4): Show | 7 | HG00735.hp1 HG01891.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1234-2286T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177490862 | ||||||
| chr2:177490871
|
T | A | 67 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(64): Show | 67 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1234-2277T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177490871 | ||||||
| chr2:177490871
|
T | TA | 6 | a0001c0001t0002g0026a0001c0001t0002g0030a0001c0001t0002g0081others(3): Show | 6 | HG03486.hp2 NA18992.hp2 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234-2274dupA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177490871 | |||||
| chr2:177491101
|
G | T | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.1234-2047G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177491101 | ||||||
| chr2:177491122
|
G | A | 1 | a0001c0001t0014g0021 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1234-2026G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177491122 | ||||||
| chr2:177491142
|
C | CCATA | 134 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(131): Show | 134 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.1234-2004_1234-200 others(8): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177491142 | |||||
| chr2:177491269
|
G | T | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.1234-1879G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177491269 | ||||||
| chr2:177491271
|
AT | A | 225 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(222): Show | 225 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.1234-1864delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177491271 | |||||
| chr2:177491402
|
G | T | 1 | a0001c0001t0001g0133 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1234-1746G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177491402 | ||||||
| chr2:177491429
|
C | CT | 45 | a0001c0001t0001g0125a0001c0001t0001g0141a0001c0001t0001g0145others(42): Show | 45 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.1234-1700dupT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177491429 | |||||
| chr2:177491646
|
T | C | 7 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(4): Show | 7 | HG01109.hp1 HG01243.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1234-1502T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177491646 | ||||||
| chr2:177491688
|
T | C | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.1234-1460T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177491688 | ||||||
| chr2:177491723
|
A | G | 1 | a0001c0001t0005g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1234-1425A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177491723 | ||||||
| chr2:177491760
|
T | C | 2 | a0001c0001t0014g0020a0001c0001t0014g0022 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1234-1388T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177491760 | ||||||
| chr2:177491760
|
T | TC | 38 | a0001c0001t0002g0025a0001c0001t0002g0029a0001c0001t0002g0035others(35): Show | 38 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1234-1375dupC | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177491760 | |||||
| chr2:177491760
|
T | TCC | 42 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0026others(39): Show | 42 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1234-1376_1234-137 others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177491760 | |||||
| chr2:177491760
|
TC | T | 96 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(93): Show | 96 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1234-1375delC | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177491760 | |||||
| chr2:177491760
|
TCC | T | 32 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(29): Show | 32 | HG00438.hp2 HG00673.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1234-1376_1234-137 others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177491760 | |||||
| chr2:177491765
|
C | G | 1 | a0001c0001t0001g0138 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1234-1383C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177491765 | ||||||
| chr2:177491772
|
C | A | 1 | a0001c0001t0001g0108 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1234-1376C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177491772 | ||||||
| chr2:177491773
|
CT | C | 6 | a0001c0001t0008g0216a0001c0001t0008g0218a0001c0001t0008g0219others(3): Show | 6 | HG01109.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234-1367delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177491773 | |||||
| chr2:177491774
|
T | C | 5 | a0001c0001t0016g0212a0001c0001t0016g0213a0001c0001t0016g0214others(2): Show | 5 | HG02055.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1234-1374T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177491774 | ||||||
| chr2:177491821
|
T | C | 1 | a0001c0001t0001g0161 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1234-1327T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177491821 | ||||||
| chr2:177491896
|
A | G | 1 | a0001c0001t0021g0027 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1234-1252A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177491896 | ||||||
| chr2:177491943
|
G | A | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1234-1205G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177491943 | ||||||
| chr2:177491996
|
C | G | 236 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(233): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1234-1152C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177491996 | ||||||
| chr2:177492146
|
T | C | 7 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(4): Show | 7 | HG00735.hp1 HG01891.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1234-1002T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177492146 | ||||||
| chr2:177492268
|
A | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1234-880A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177492268 | ||||||
| chr2:177492309
|
A | G | 2 | a0001c0001t0002g0053a0001c0001t0002g0249 | 2 | HG02074.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.1234-839A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177492309 | ||||||
| chr2:177492423
|
T | G | 1 | a0001c0001t0001g0117 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1234-725T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177492423 | ||||||
| chr2:177492551
|
A | G | 1 | a0001c0001t0003g0231 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1234-597A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177492551 | ||||||
| chr2:177492728
|
T | C | 1 | a0001c0001t0007g0034 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1234-420T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177492728 | ||||||
| chr2:177492734
|
TA | T | 3 | a0001c0001t0013g0018a0001c0001t0037g0019a0001c0002t0013g0206 | 3 | HG02109.hp1 HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1234-410delA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | 177492734 | |||||
| chr2:177492845
|
G | A | 2 | a0001c0001t0027g0226a0001c0001t0028g0227 | 2 | HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1234-303G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177492845 | ||||||
| chr2:177492916
|
T | TAAA | 113 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(110): Show | 113 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1234-232_1234-231i others(5): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177492916 | ||||||
| chr2:177492917
|
G | C | 114 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(111): Show | 114 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1234-231G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177492917 | ||||||
| chr2:177492920
|
T | C | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1234-228T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177492920 | ||||||
| chr2:177493109
|
A | G | 12 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1234-39A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 11/19 | chr2 | 177493109 | ||||||
| chr2:177493344
|
C | T | 134 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(131): Show | 134 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.1285+145C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177493344 | ||||||
| chr2:177493406
|
G | A | 2 | a0001c0002t0004g0010a0001c0002t0004g0011 | 2 | HG02698.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1285+207G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177493406 | ||||||
| chr2:177493505
|
G | T | 134 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(131): Show | 134 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.1285+306G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177493505 | ||||||
| chr2:177493529
|
CTCT | C | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1285+340_1285+342d others(5): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr2 | 177493529 | |||||
| chr2:177493553
|
C | T | 92 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(89): Show | 92 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1285+354C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177493553 | ||||||
| chr2:177493614
|
A | G | 2 | a0001c0001t0033g0195a0001c0001t0035g0017 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1285+415A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177493614 | ||||||
| chr2:177493617
|
T | C | 257 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(254): Show | 257 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(254): Show |
intron_variant | MODIFIER | c.1285+418T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177493617 | ||||||
| chr2:177493645
|
G | C | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1285+446G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177493645 | ||||||
| chr2:177493673
|
G | C | 18 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(15): Show | 18 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1285+474G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177493673 | ||||||
| chr2:177493696
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1285+497A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177493696 | ||||||
| chr2:177493924
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1285+725T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177493924 | ||||||
| chr2:177494146
|
G | A | 7 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(4): Show | 7 | HG00735.hp1 HG01891.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1285+947G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177494146 | ||||||
| chr2:177494273
|
A | T | 2 | a0001c0001t0033g0195a0001c0001t0035g0017 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1285+1074A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177494273 | ||||||
| chr2:177494350
|
A | G | 1 | a0001c0001t0020g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1285+1151A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177494350 | ||||||
| chr2:177494472
|
A | G | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.1285+1273A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177494472 | ||||||
| chr2:177494848
|
A | G | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.1285+1649A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177494848 | ||||||
| chr2:177495177
|
G | A | 2 | a0001c0001t0037g0019a0001c0002t0013g0206 | 2 | HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1285+1978G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177495177 | ||||||
| chr2:177495311
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1285+2112A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177495311 | ||||||
| chr2:177495333
|
A | G | 4 | a0001c0001t0002g0030a0001c0001t0002g0058a0001c0001t0002g0060others(1): Show | 4 | NA18950.hp1 NA18981.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1285+2134A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177495333 | ||||||
| chr2:177495347
|
G | A | 18 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231others(15): Show | 18 | HG00642.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.1285+2148G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177495347 | ||||||
| chr2:177495745
|
T | TA | 119 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(116): Show | 119 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.1286-1929dupA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr2 | 177495745 | |||||
| chr2:177495745
|
T | TAA | 98 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(95): Show | 98 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1286-1930_1286-192 others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr2 | 177495745 | |||||
| chr2:177495745
|
T | TAAA | 5 | a0001c0001t0001g0157a0001c0001t0001g0160a0001c0001t0009g0162others(2): Show | 5 | HG01175.hp1 HG02027.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1286-1931_1286-192 others(7): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr2 | 177495745 | |||||
| chr2:177495782
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1286-1907T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177495782 | ||||||
| chr2:177495822
|
G | T | 1 | a0001c0002t0048g0008 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1286-1867G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177495822 | ||||||
| chr2:177495842
|
G | A | 3 | a0001c0001t0002g0030a0001c0001t0002g0058a0001c0001t0002g0060 | 3 | NA18950.hp1 NA18998.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1286-1847G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177495842 | ||||||
| chr2:177495887
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1286-1802C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177495887 | ||||||
| chr2:177495907
|
G | A | 1 | a0001c0002t0048g0008 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1286-1782G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177495907 | ||||||
| chr2:177495911
|
C | T | 2 | a0001c0001t0033g0195a0001c0001t0035g0017 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1286-1778C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177495911 | ||||||
| chr2:177495917
|
CA | C | 8 | a0001c0001t0002g0023a0001c0001t0002g0039a0001c0001t0002g0041others(5): Show | 8 | HG01258.hp2 HG03209.hp2 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.1286-1751delA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr2 | 177495917 | |||||
| chr2:177495917
|
CAA | C | 40 | a0001c0001t0001g0106a0001c0001t0001g0125a0001c0001t0001g0131others(37): Show | 40 | HG00597.hp1 HG00673.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.1286-1752_1286-175 others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr2 | 177495917 | |||||
| chr2:177495917
|
CAAA | C | 182 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(179): Show | 182 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.1286-1753_1286-175 others(7): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr2 | 177495917 | |||||
| chr2:177496406
|
G | A | 4 | a0001c0001t0003g0242a0001c0001t0017g0207a0001c0001t0017g0208others(1): Show | 4 | HG02886.hp2 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1286-1283G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177496406 | ||||||
| chr2:177496541
|
G | A | 2 | a0001c0001t0018g0215a0001c0001t0018g0221 | 2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1286-1148G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177496541 | ||||||
| chr2:177496718
|
A | T | 1 | a0001c0001t0033g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1286-971A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177496718 | ||||||
| chr2:177496918
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1286-771A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177496918 | ||||||
| chr2:177497002
|
A | T | 1 | a0001c0001t0003g0241 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1286-687A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177497002 | ||||||
| chr2:177497167
|
C | T | 2 | a0001c0001t0027g0226a0001c0001t0028g0227 | 2 | HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1286-522C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177497167 | ||||||
| chr2:177497561
|
C | T | 5 | a0001c0001t0002g0036a0001c0001t0002g0067a0001c0001t0002g0068others(2): Show | 5 | NA18943.hp1 NA18944.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.1286-128C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 12/19 | chr2 | 177497561 | ||||||
| chr2:177497844
|
G | A | 236 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(233): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1362+79G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 13/19 | chr2 | 177497844 | ||||||
| chr2:177498084
|
C | T | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1362+319C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 13/19 | chr2 | 177498084 | ||||||
| chr2:177498136
|
G | A | 15 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(12): Show | 15 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1362+371G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 13/19 | chr2 | 177498136 | ||||||
| chr2:177498372
|
G | A | 15 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(12): Show | 15 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1362+607G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 13/19 | chr2 | 177498372 | ||||||
| chr2:177498435
|
A | G | 1 | a0001c0001t0039g0164 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1362+670A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 13/19 | chr2 | 177498435 | ||||||
| chr2:177498539
|
T | C | 1 | a0001c0001t0032g0210 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1362+774T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 13/19 | chr2 | 177498539 | ||||||
| chr2:177498573
|
T | A | 23 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231others(20): Show | 23 | HG00642.hp2 HG01167.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.1362+808T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 13/19 | chr2 | 177498573 | ||||||
| chr2:177498625
|
AT | A | 17 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231others(14): Show | 17 | HG00642.hp2 HG01167.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1362+863delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr2 | 177498625 | |||||
| chr2:177498628
|
T | A | 5 | a0001c0001t0001g0117a0001c0001t0001g0140a0001c0001t0003g0241others(2): Show | 5 | HG00735.hp2 HG00738.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1362+863T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 13/19 | chr2 | 177498628 | ||||||
| chr2:177498628
|
TA | T | 6 | a0001c0001t0002g0060a0001c0001t0011g0245a0001c0001t0011g0246others(3): Show | 6 | HG02132.hp1 HG02165.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.1362+875delA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr2 | 177498628 | |||||
| chr2:177498695
|
T | C | 113 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(110): Show | 113 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1363-923T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 13/19 | chr2 | 177498695 | ||||||
| chr2:177498738
|
C | T | 1 | a0001c0001t0003g0233 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1363-880C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 13/19 | chr2 | 177498738 | ||||||
| chr2:177499223
|
G | A | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1363-395G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 13/19 | chr2 | 177499223 | ||||||
| chr2:177499254
|
C | T | 1 | a0001c0001t0002g0088 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1363-364C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 13/19 | chr2 | 177499254 | ||||||
| chr2:177499273
|
C | G | 7 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(4): Show | 7 | HG01109.hp1 HG01243.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1363-345C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 13/19 | chr2 | 177499273 | ||||||
| chr2:177499600
|
A | T | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1363-18A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 13/19 | chr2 | 177499600 | ||||||
| chr2:177499763
|
G | C | 12 | a0001c0002t0004g0002a0001c0002t0004g0003a0001c0002t0004g0004others(9): Show | 12 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.1475+33G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177499763 | ||||||
| chr2:177500077
|
T | G | 13 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(10): Show | 13 | HG01361.hp1 HG01884.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1475+347T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177500077 | ||||||
| chr2:177500172
|
T | C | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1475+442T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177500172 | ||||||
| chr2:177500554
|
AT | A | 13 | a0001c0001t0004g0093a0001c0002t0004g0002a0001c0002t0004g0003others(10): Show | 13 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.1475+832delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr2 | 177500554 | |||||
| chr2:177500653
|
A | G | 74 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(71): Show | 74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1475+923A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177500653 | ||||||
| chr2:177500974
|
C | T | 15 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(12): Show | 15 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1475+1244C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177500974 | ||||||
| chr2:177501028
|
A | G | 2 | a0001c0001t0025g0253a0001c0001t0025g0254 | 2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1475+1298A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177501028 | ||||||
| chr2:177501093
|
G | T | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1475+1363G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177501093 | ||||||
| chr2:177501244
|
C | T | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1475+1514C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177501244 | ||||||
| chr2:177501252
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1475+1522T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177501252 | ||||||
| chr2:177501522
|
T | G | 1 | a0001c0001t0004g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1475+1792T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177501522 | ||||||
| chr2:177501675
|
G | A | 69 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(66): Show | 69 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1475+1945G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177501675 | ||||||
| chr2:177501690
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1475+1960C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177501690 | ||||||
| chr2:177501717
|
G | C | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1475+1987G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177501717 | ||||||
| chr2:177501825
|
G | A | 1 | a0001c0001t0005g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1475+2095G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177501825 | ||||||
| chr2:177501879
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0153 | 2 | HG01255.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1475+2149G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177501879 | ||||||
| chr2:177501888
|
G | A | 5 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(2): Show | 5 | HG02027.hp1 HG02132.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1475+2158G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177501888 | ||||||
| chr2:177501983
|
A | G | 1 | a0001c0001t0002g0033 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1475+2253A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177501983 | ||||||
| chr2:177502250
|
AT | A | 223 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(220): Show | 223 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.1475+2532delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr2 | 177502250 | |||||
| chr2:177502376
|
CAGATTAC others(2): Show |
C | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1475+2659_1475+266 others(13): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr2 | 177502376 | |||||
| chr2:177502407
|
AT | A | 27 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231others(24): Show | 27 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.1475+2700delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr2 | 177502407 | |||||
| chr2:177502407
|
ATT | A | 8 | a0001c0001t0001g0106a0001c0001t0001g0163a0001c0001t0014g0020others(5): Show | 8 | HG01169.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1475+2699_1475+270 others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr2 | 177502407 | |||||
| chr2:177502407
|
ATTT | A | 59 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(56): Show | 59 | HG00642.hp1 HG01081.hp1 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.1475+2698_1475+270 others(7): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr2 | 177502407 | |||||
| chr2:177502407
|
ATTTT | A | 88 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0115others(85): Show | 88 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1475+2697_1475+270 others(8): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr2 | 177502407 | |||||
| chr2:177502407
|
ATTTTT | A | 64 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0194others(61): Show | 64 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1475+2696_1475+270 others(9): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr2 | 177502407 | |||||
| chr2:177502513
|
C | T | 1 | a0001c0001t0036g0046 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1475+2783C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177502513 | ||||||
| chr2:177502702
|
G | A | 233 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(230): Show | 233 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.1476-2804G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177502702 | ||||||
| chr2:177502880
|
A | AC | 234 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(231): Show | 234 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.1476-2624dupC | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr2 | 177502880 | |||||
| chr2:177503004
|
CATCT | C | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1476-2498_1476-249 others(8): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr2 | 177503004 | |||||
| chr2:177503156
|
A | G | 2 | a0001c0001t0033g0195a0001c0001t0035g0017 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1476-2350A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177503156 | ||||||
| chr2:177503373
|
G | A | 10 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(7): Show | 10 | HG00735.hp1 HG01891.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1476-2133G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177503373 | ||||||
| chr2:177503379
|
G | A | 1 | a0001c0001t0003g0241 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1476-2127G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177503379 | ||||||
| chr2:177503510
|
A | T | 2 | a0001c0002t0004g0003a0001c0002t0004g0005 | 2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1476-1996A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177503510 | ||||||
| chr2:177503524
|
G | A | 1 | a0001c0001t0041g0099 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1476-1982G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177503524 | ||||||
| chr2:177503615
|
G | A | 7 | a0001c0001t0001g0118a0001c0001t0001g0127a0001c0001t0001g0178others(4): Show | 7 | HG00639.hp2 HG01081.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1476-1891G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177503615 | ||||||
| chr2:177503791
|
ACT | A | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1476-1712_1476-171 others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr2 | 177503791 | |||||
| chr2:177503808
|
T | C | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1476-1698T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177503808 | ||||||
| chr2:177504057
|
A | C | 2 | a0001c0001t0025g0253a0001c0001t0025g0254 | 2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1476-1449A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177504057 | ||||||
| chr2:177504269
|
C | A | 229 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(226): Show | 229 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.1476-1237C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177504269 | ||||||
| chr2:177504308
|
G | C | 137 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(134): Show | 137 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.1476-1198G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177504308 | ||||||
| chr2:177504319
|
T | TTA | 229 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(226): Show | 229 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.1476-1187_1476-118 others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177504319 | ||||||
| chr2:177504320
|
G | T | 229 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(226): Show | 229 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.1476-1186G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177504320 | ||||||
| chr2:177504321
|
G | T | 229 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(226): Show | 229 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.1476-1185G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177504321 | ||||||
| chr2:177504322
|
A | T | 229 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(226): Show | 229 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.1476-1184A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177504322 | ||||||
| chr2:177504415
|
G | A | 15 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(12): Show | 15 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1476-1091G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177504415 | ||||||
| chr2:177504515
|
A | C | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1476-991A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177504515 | ||||||
| chr2:177504705
|
T | C | 229 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(226): Show | 229 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.1476-801T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177504705 | ||||||
| chr2:177504873
|
C | A | 1 | a0001c0001t0001g0151 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1476-633C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177504873 | ||||||
| chr2:177504988
|
C | T | 1 | a0001c0001t0002g0086 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1476-518C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177504988 | ||||||
| chr2:177505052
|
G | A | 1 | a0001c0001t0004g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1476-454G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177505052 | ||||||
| chr2:177505083
|
TAAAC | T | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1476-421_1476-418d others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr2 | 177505083 | |||||
| chr2:177505312
|
T | C | 233 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(230): Show | 233 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.1476-194T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177505312 | ||||||
| chr2:177505445
|
A | T | 1 | a0001c0001t0006g0047 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1476-61A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 14/19 | chr2 | 177505445 | ||||||
| chr2:177505652
|
T | A | 24 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(21): Show | 24 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.1545+77T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | chr2 | 177505652 | ||||||
| chr2:177505700
|
C | T | 15 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(12): Show | 15 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1545+125C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | chr2 | 177505700 | ||||||
| chr2:177505792
|
A | G | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1545+217A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | chr2 | 177505792 | ||||||
| chr2:177505897
|
C | T | 255 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(252): Show | 255 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.1545+322C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | chr2 | 177505897 | ||||||
| chr2:177505903
|
A | G | 229 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(226): Show | 229 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.1545+328A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | chr2 | 177505903 | ||||||
| chr2:177506184
|
A | G | 2 | a0001c0001t0002g0056a0001c0001t0003g0240 | 2 | HG04199.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1545+609A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | chr2 | 177506184 | ||||||
| chr2:177506219
|
C | CT | 232 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(229): Show | 232 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.1545+651dupT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr2 | 177506219 | |||||
| chr2:177506393
|
C | T | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1545+818C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | chr2 | 177506393 | ||||||
| chr2:177506420
|
A | G | 2 | a0001c0001t0037g0019a0001c0002t0013g0206 | 2 | HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1545+845A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | chr2 | 177506420 | ||||||
| chr2:177506651
|
C | T | 68 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(65): Show | 68 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1545+1076C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | chr2 | 177506651 | ||||||
| chr2:177506761
|
A | T | 1 | a0001c0001t0022g0134 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1545+1186A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | chr2 | 177506761 | ||||||
| chr2:177506888
|
CT | C | 5 | a0001c0001t0016g0212a0001c0001t0016g0213a0001c0001t0016g0214others(2): Show | 5 | HG02055.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1546-1078delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr2 | 177506888 | |||||
| chr2:177506897
|
A | C | 5 | a0001c0001t0016g0212a0001c0001t0016g0213a0001c0001t0016g0214others(2): Show | 5 | HG02055.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1546-1073A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | chr2 | 177506897 | ||||||
| chr2:177506946
|
A | G | 2 | a0001c0002t0004g0010a0001c0002t0004g0011 | 2 | HG02698.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1546-1024A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | chr2 | 177506946 | ||||||
| chr2:177507011
|
G | T | 112 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(109): Show | 112 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1546-959G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | chr2 | 177507011 | ||||||
| chr2:177507041
|
CT | C | 6 | a0001c0001t0015g0223a0001c0001t0015g0224a0001c0001t0015g0225others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1546-928delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | chr2 | 177507041 | ||||||
| chr2:177507193
|
C | T | 233 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(230): Show | 233 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.1546-777C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | chr2 | 177507193 | ||||||
| chr2:177507216
|
T | C | 15 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(12): Show | 15 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1546-754T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | chr2 | 177507216 | ||||||
| chr2:177507463
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0159 | 2 | HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1546-507G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | chr2 | 177507463 | ||||||
| chr2:177507601
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1546-369C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | chr2 | 177507601 | ||||||
| chr2:177507730
|
C | T | 1 | a0001c0001t0008g0218 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1546-240C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 15/19 | chr2 | 177507730 | ||||||
| chr2:177508096
|
T | C | 5 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(2): Show | 5 | HG02027.hp1 HG02132.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1607+65T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177508096 | ||||||
| chr2:177508202
|
G | A | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1607+171G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177508202 | ||||||
| chr2:177508397
|
C | T | 1 | a0001c0001t0005g0200 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1607+366C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177508397 | ||||||
| chr2:177508434
|
A | G | 2 | a0001c0001t0021g0027a0001c0001t0021g0028 | 2 | HG00438.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1607+403A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177508434 | ||||||
| chr2:177508724
|
C | T | 228 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(225): Show | 228 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.1607+693C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177508724 | ||||||
| chr2:177508924
|
G | T | 137 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(134): Show | 137 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.1607+893G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177508924 | ||||||
| chr2:177509160
|
G | A | 1 | a0001c0003t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1607+1129G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177509160 | ||||||
| chr2:177509384
|
C | T | 228 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(225): Show | 228 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.1607+1353C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177509384 | ||||||
| chr2:177509430
|
G | A | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1607+1399G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177509430 | ||||||
| chr2:177509447
|
A | G | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1607+1416A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177509447 | ||||||
| chr2:177509615
|
G | C | 1 | a0001c0001t0003g0231 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1607+1584G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177509615 | ||||||
| chr2:177509624
|
T | C | 251 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(248): Show | 251 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(248): Show |
intron_variant | MODIFIER | c.1607+1593T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177509624 | ||||||
| chr2:177509653
|
G | A | 69 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(66): Show | 69 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1607+1622G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177509653 | ||||||
| chr2:177509665
|
CA | C | 218 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(215): Show | 218 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.1607+1650delA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr2 | 177509665 | |||||
| chr2:177509903
|
G | A | 1 | a0001c0002t0004g0011 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1607+1872G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177509903 | ||||||
| chr2:177509905
|
A | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1607+1874A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177509905 | ||||||
| chr2:177510036
|
C | A | 2 | a0001c0001t0003g0232a0001c0001t0003g0235 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1607+2005C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177510036 | ||||||
| chr2:177510060
|
G | T | 234 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(231): Show | 234 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.1607+2029G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177510060 | ||||||
| chr2:177510337
|
C | A | 233 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(230): Show | 233 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.1607+2306C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177510337 | ||||||
| chr2:177510368
|
C | T | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1607+2337C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177510368 | ||||||
| chr2:177510394
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1607+2363T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177510394 | ||||||
| chr2:177510907
|
C | T | 7 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(4): Show | 7 | HG01109.hp1 HG01243.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1607+2876C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177510907 | ||||||
| chr2:177511221
|
T | C | 5 | a0001c0001t0002g0023a0001c0001t0002g0039a0001c0001t0002g0041others(2): Show | 5 | NA18963.hp2 NA18965.hp1 NA19087.hp1 others(2): Show |
intron_variant | MODIFIER | c.1608-2598T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177511221 | ||||||
| chr2:177511336
|
G | C | 1 | a0001c0001t0032g0210 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1608-2483G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177511336 | ||||||
| chr2:177511417
|
A | G | 15 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(12): Show | 15 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1608-2402A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177511417 | ||||||
| chr2:177511447
|
A | G | 15 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(12): Show | 15 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1608-2372A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177511447 | ||||||
| chr2:177511547
|
A | T | 3 | a0001c0001t0013g0018a0001c0001t0037g0019a0001c0002t0013g0206 | 3 | HG02109.hp1 HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1608-2272A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177511547 | ||||||
| chr2:177511952
|
G | T | 68 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(65): Show | 68 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1608-1867G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177511952 | ||||||
| chr2:177511955
|
C | T | 68 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(65): Show | 68 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1608-1864C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177511955 | ||||||
| chr2:177511956
|
A | G | 229 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(226): Show | 229 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.1608-1863A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177511956 | ||||||
| chr2:177512224
|
CAT | C | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1608-1592_1608-159 others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr2 | 177512224 | |||||
| chr2:177512405
|
C | G | 229 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(226): Show | 229 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.1608-1414C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177512405 | ||||||
| chr2:177512519
|
A | G | 2 | a0001c0001t0023g0074a0001c0001t0023g0075 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1608-1300A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177512519 | ||||||
| chr2:177512583
|
G | A | 136 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(133): Show | 136 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1608-1236G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177512583 | ||||||
| chr2:177513065
|
A | G | 70 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(67): Show | 70 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1608-754A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177513065 | ||||||
| chr2:177513085
|
CATT | C | 233 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(230): Show | 233 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.1608-715_1608-713d others(5): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr2 | 177513085 | |||||
| chr2:177513165
|
G | C | 1 | a0001c0001t0033g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1608-654G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177513165 | ||||||
| chr2:177513171
|
T | A | 1 | a0001c0001t0004g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1608-648T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177513171 | ||||||
| chr2:177513424
|
G | T | 1 | a0001c0001t0002g0055 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1608-395G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177513424 | ||||||
| chr2:177513447
|
C | A | 234 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(231): Show | 234 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.1608-372C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177513447 | ||||||
| chr2:177513535
|
G | A | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1608-284G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177513535 | ||||||
| chr2:177513576
|
G | A | 1 | a0001c0001t0013g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1608-243G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177513576 | ||||||
| chr2:177513724
|
T | A | 92 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(89): Show | 92 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1608-95T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 16/19 | chr2 | 177513724 | ||||||
| chr2:177514138
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1697+230C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177514138 | ||||||
| chr2:177514522
|
TC | T | 10 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(7): Show | 10 | HG00735.hp1 HG01891.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1697+615delC | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177514522 | ||||||
| chr2:177514666
|
A | G | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1697+758A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177514666 | ||||||
| chr2:177514729
|
A | G | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1697+821A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177514729 | ||||||
| chr2:177514752
|
C | A | 2 | a0001c0001t0033g0195a0001c0001t0035g0017 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1697+844C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177514752 | ||||||
| chr2:177514881
|
G | A | 1 | a0001c0001t0024g0174 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1697+973G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177514881 | ||||||
| chr2:177515055
|
G | C | 229 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(226): Show | 229 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.1697+1147G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177515055 | ||||||
| chr2:177515283
|
A | G | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1697+1375A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177515283 | ||||||
| chr2:177515514
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1697+1606C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177515514 | ||||||
| chr2:177515681
|
A | G | 140 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(137): Show | 140 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.1697+1773A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177515681 | ||||||
| chr2:177515782
|
G | A | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1697+1874G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177515782 | ||||||
| chr2:177515813
|
G | C | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1697+1905G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177515813 | ||||||
| chr2:177515917
|
T | C | 91 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(88): Show | 91 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1697+2009T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177515917 | ||||||
| chr2:177515950
|
TG | T | 230 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(227): Show | 230 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.1697+2044delG | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr2 | 177515950 | |||||
| chr2:177516142
|
G | A | 1 | a0001c0001t0018g0215 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1697+2234G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177516142 | ||||||
| chr2:177516312
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1697+2404C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177516312 | ||||||
| chr2:177516376
|
G | A | 2 | a0001c0001t0021g0027a0001c0001t0021g0028 | 2 | HG00438.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1697+2468G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177516376 | ||||||
| chr2:177516388
|
A | T | 231 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(228): Show | 231 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.1697+2480A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177516388 | ||||||
| chr2:177516395
|
T | A | 15 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(12): Show | 15 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1697+2487T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177516395 | ||||||
| chr2:177516846
|
C | G | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1697+2938C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177516846 | ||||||
| chr2:177516869
|
C | T | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1697+2961C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177516869 | ||||||
| chr2:177517089
|
A | C | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1697+3181A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177517089 | ||||||
| chr2:177517368
|
GCTTA | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1697+3463_1697+346 others(8): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr2 | 177517368 | |||||
| chr2:177517611
|
T | C | 2 | a0001c0001t0005g0250a0001c0001t0005g0251 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1698-3658T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177517611 | ||||||
| chr2:177517697
|
A | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1698-3572A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177517697 | ||||||
| chr2:177517715
|
C | A | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1698-3554C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177517715 | ||||||
| chr2:177517895
|
T | C | 91 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(88): Show | 91 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1698-3374T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177517895 | ||||||
| chr2:177518308
|
C | T | 136 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(133): Show | 136 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1698-2961C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177518308 | ||||||
| chr2:177518364
|
A | G | 74 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(71): Show | 74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1698-2905A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177518364 | ||||||
| chr2:177518424
|
A | G | 233 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(230): Show | 233 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.1698-2845A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177518424 | ||||||
| chr2:177518468
|
G | A | 15 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(12): Show | 15 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1698-2801G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177518468 | ||||||
| chr2:177518489
|
A | G | 2 | a0001c0001t0025g0253a0001c0001t0025g0254 | 2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1698-2780A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177518489 | ||||||
| chr2:177518669
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1698-2600G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177518669 | ||||||
| chr2:177518900
|
A | G | 15 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(12): Show | 15 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1698-2369A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177518900 | ||||||
| chr2:177519361
|
C | A | 1 | a0001c0001t0002g0026 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1698-1908C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177519361 | ||||||
| chr2:177519363
|
T | A | 1 | a0001c0001t0001g0163 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1698-1906T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177519363 | ||||||
| chr2:177519471
|
C | G | 2 | a0001c0002t0009g0204a0001c0002t0034g0211 | 2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1698-1798C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177519471 | ||||||
| chr2:177519523
|
C | G | 1 | a0001c0001t0005g0201 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1698-1746C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177519523 | ||||||
| chr2:177519541
|
T | G | 7 | a0001c0001t0001g0096a0001c0001t0001g0100a0001c0001t0001g0101others(4): Show | 7 | HG01361.hp1 HG01884.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1698-1728T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177519541 | ||||||
| chr2:177519570
|
T | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0159 | 2 | HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1698-1699T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177519570 | ||||||
| chr2:177520085
|
G | A | 2 | a0001c0001t0023g0074a0001c0001t0023g0075 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1698-1184G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177520085 | ||||||
| chr2:177520139
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1698-1130C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177520139 | ||||||
| chr2:177520406
|
G | A | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1698-863G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177520406 | ||||||
| chr2:177520445
|
G | A | 1 | a0001c0001t0020g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1698-824G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177520445 | ||||||
| chr2:177520521
|
C | T | 2 | a0001c0002t0004g0012a0001c0002t0004g0013 | 2 | HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1698-748C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177520521 | ||||||
| chr2:177520524
|
CTGTTTAC others(2): Show |
C | 72 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(69): Show | 72 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1698-742_1698-734d others(11): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr2 | 177520524 | |||||
| chr2:177520755
|
G | A | 1 | a0001c0001t0015g0225 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1698-514G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177520755 | ||||||
| chr2:177520831
|
C | CTA | 5 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(2): Show | 5 | HG02027.hp1 HG02132.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1698-428_1698-427d others(4): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr2 | 177520831 | |||||
| chr2:177520839
|
ATATT | A | 15 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(12): Show | 15 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1698-429_1698-426d others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177520839 | ||||||
| chr2:177521255
|
T | C | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1698-14T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 17/19 | chr2 | 177521255 | ||||||
| chr2:177521432
|
C | G | 3 | a0001c0001t0010g0123a0001c0001t0010g0147a0001c0001t0010g0205 | 3 | HG00544.hp2 HG00597.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1797+64C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 18/19 | chr2 | 177521432 | ||||||
| chr2:177522372
|
A | T | 233 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(230): Show | 233 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.1797+1004A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 18/19 | chr2 | 177522372 | ||||||
| chr2:177522380
|
G | A | 6 | a0001c0001t0012g0014a0001c0001t0012g0015a0001c0001t0012g0016others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1797+1012G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 18/19 | chr2 | 177522380 | ||||||
| chr2:177522404
|
C | A | 1 | a0001c0001t0003g0230 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1797+1036C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 18/19 | chr2 | 177522404 | ||||||
| chr2:177522662
|
C | G | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1798-1086C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 18/19 | chr2 | 177522662 | ||||||
| chr2:177522819
|
C | T | 90 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(87): Show | 90 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1798-929C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 18/19 | chr2 | 177522819 | ||||||
| chr2:177522887
|
G | C | 69 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(66): Show | 69 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1798-861G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 18/19 | chr2 | 177522887 | ||||||
| chr2:177523007
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1798-741A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 18/19 | chr2 | 177523007 | ||||||
| chr2:177523163
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1798-585A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 18/19 | chr2 | 177523163 | ||||||
| chr2:177523436
|
T | G | 70 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(67): Show | 70 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1798-312T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 18/19 | chr2 | 177523436 | ||||||
| chr2:177524207
|
G | A | 1 | a0001c0003t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1855+402G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177524207 | ||||||
| chr2:177524322
|
C | T | 5 | a0001c0001t0002g0050a0001c0001t0002g0053a0001c0001t0002g0057others(2): Show | 5 | HG02074.hp2 NA18941.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.1855+517C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177524322 | ||||||
| chr2:177524414
|
C | A | 1 | a0001c0001t0001g0139 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1855+609C>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177524414 | ||||||
| chr2:177524540
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1855+735T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177524540 | ||||||
| chr2:177524581
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1855+776T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177524581 | ||||||
| chr2:177524632
|
CT | C | 15 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(12): Show | 15 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1855+835delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 177524632 | |||||
| chr2:177524674
|
A | G | 5 | a0001c0001t0016g0212a0001c0001t0016g0213a0001c0001t0016g0214others(2): Show | 5 | HG02055.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1855+869A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177524674 | ||||||
| chr2:177524883
|
T | C | 15 | a0001c0001t0004g0093a0001c0001t0025g0253a0001c0001t0025g0254others(12): Show | 15 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1855+1078T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177524883 | ||||||
| chr2:177525041
|
C | T | 5 | a0001c0001t0016g0212a0001c0001t0016g0213a0001c0001t0016g0214others(2): Show | 5 | HG02055.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1855+1236C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177525041 | ||||||
| chr2:177525103
|
A | G | 2 | a0001c0001t0033g0195a0001c0001t0035g0017 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1855+1298A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177525103 | ||||||
| chr2:177525322
|
T | C | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG00642.hp1 HG01257.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.1855+1517T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177525322 | ||||||
| chr2:177525364
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1855+1559G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177525364 | ||||||
| chr2:177525701
|
G | A | 229 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(226): Show | 229 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.1855+1896G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177525701 | ||||||
| chr2:177525810
|
T | G | 9 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(6): Show | 9 | HG00408.hp1 HG00438.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.1855+2005T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177525810 | ||||||
| chr2:177525815
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1855+2010T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177525815 | ||||||
| chr2:177525880
|
A | G | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1855+2075A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177525880 | ||||||
| chr2:177526009
|
G | A | 1 | a0001c0002t0004g0011 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1855+2204G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177526009 | ||||||
| chr2:177526050
|
T | C | 228 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(225): Show | 228 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.1855+2245T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177526050 | ||||||
| chr2:177526227
|
C | CT | 13 | a0001c0001t0001g0112a0001c0001t0001g0175a0001c0001t0001g0183others(10): Show | 13 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1855+2442dupT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 177526227 | |||||
| chr2:177526227
|
C | CTTT | 8 | a0001c0001t0005g0104a0001c0001t0005g0197a0001c0001t0005g0198others(5): Show | 8 | HG00735.hp1 HG01891.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1855+2440_1855+244 others(7): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 177526227 | |||||
| chr2:177526227
|
CT | C | 73 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1855+2442delT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 177526227 | |||||
| chr2:177526473
|
G | A | 1 | a0001c0001t0033g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1855+2668G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177526473 | ||||||
| chr2:177526619
|
G | A | 3 | a0001c0001t0010g0123a0001c0001t0010g0147a0001c0001t0010g0205 | 3 | HG00544.hp2 HG00597.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1855+2814G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177526619 | ||||||
| chr2:177526631
|
A | G | 4 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0055others(1): Show | 4 | HG00738.hp2 HG01496.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1855+2826A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177526631 | ||||||
| chr2:177526713
|
T | C | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1855+2908T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177526713 | ||||||
| chr2:177526852
|
G | A | 72 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(69): Show | 72 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1855+3047G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177526852 | ||||||
| chr2:177526939
|
A | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1855+3134A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177526939 | ||||||
| chr2:177526978
|
A | G | 1 | a0001c0001t0002g0041 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1855+3173A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177526978 | ||||||
| chr2:177527198
|
C | T | 1 | a0001c0001t0007g0064 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1855+3393C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177527198 | ||||||
| chr2:177527289
|
A | G | 1 | a0001c0001t0004g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1855+3484A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177527289 | ||||||
| chr2:177527351
|
C | G | 1 | a0001c0001t0024g0098 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1855+3546C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177527351 | ||||||
| chr2:177527604
|
A | T | 230 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(227): Show | 230 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.1855+3799A>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177527604 | ||||||
| chr2:177527618
|
A | G | 135 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(132): Show | 135 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.1855+3813A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177527618 | ||||||
| chr2:177527827
|
G | A | 74 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(71): Show | 74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1855+4022G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177527827 | ||||||
| chr2:177528190
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1855+4385C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177528190 | ||||||
| chr2:177528230
|
A | G | 74 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(71): Show | 74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1855+4425A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177528230 | ||||||
| chr2:177528449
|
C | T | 1 | a0001c0001t0015g0225 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1855+4644C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177528449 | ||||||
| chr2:177528596
|
G | A | 72 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(69): Show | 72 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1855+4791G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177528596 | ||||||
| chr2:177528718
|
T | C | 1 | a0001c0001t0009g0091 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1855+4913T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177528718 | ||||||
| chr2:177528849
|
C | CT | 104 | a0001c0001t0001g0094a0001c0001t0001g0105a0001c0001t0001g0106others(101): Show | 104 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1855+5067dupT | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 177528849 | |||||
| chr2:177528849
|
C | CTT | 34 | a0001c0001t0001g0128a0001c0001t0001g0167a0001c0001t0001g0175others(31): Show | 34 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1855+5066_1855+506 others(6): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 177528849 | |||||
| chr2:177528849
|
C | CTTT | 69 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(66): Show | 69 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1855+5065_1855+506 others(7): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 177528849 | |||||
| chr2:177528849
|
C | CTTTT | 14 | a0001c0001t0002g0031a0001c0001t0002g0036a0001c0001t0002g0037others(11): Show | 14 | HG00423.hp1 HG01257.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1855+5064_1855+506 others(8): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 177528849 | |||||
| chr2:177529004
|
C | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0189a0001c0001t0001g0190 | 3 | HG02698.hp1 NA18939.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1855+5199C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177529004 | ||||||
| chr2:177529045
|
C | T | 77 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(74): Show | 77 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1855+5240C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177529045 | ||||||
| chr2:177529152
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1855+5347C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177529152 | ||||||
| chr2:177529277
|
G | A | 10 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0097others(7): Show | 10 | HG01361.hp1 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1855+5472G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177529277 | ||||||
| chr2:177529506
|
T | C | 230 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(227): Show | 230 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.1855+5701T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177529506 | ||||||
| chr2:177529625
|
T | G | 2 | a0001c0001t0033g0195a0001c0001t0035g0017 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1855+5820T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177529625 | ||||||
| chr2:177529626
|
GAGTT | G | 3 | a0001c0002t0004g0002a0001c0002t0004g0004a0001c0002t0004g0007 | 3 | HG02055.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1855+5827_1855+583 others(8): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 177529626 | |||||
| chr2:177530109
|
A | G | 2 | a0001c0002t0009g0204a0001c0002t0034g0211 | 2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1855+6304A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177530109 | ||||||
| chr2:177530129
|
A | G | 1 | a0001c0001t0002g0090 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1855+6324A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177530129 | ||||||
| chr2:177530142
|
A | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1855+6337A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177530142 | ||||||
| chr2:177530199
|
A | G | 6 | a0001c0001t0012g0014a0001c0001t0012g0015a0001c0001t0012g0016others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1855+6394A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177530199 | ||||||
| chr2:177530274
|
G | A | 10 | a0001c0001t0005g0104a0001c0001t0005g0197a0001c0001t0005g0198others(7): Show | 10 | HG00735.hp1 HG01891.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1855+6469G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177530274 | ||||||
| chr2:177530329
|
G | A | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.1855+6524G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177530329 | ||||||
| chr2:177530363
|
G | T | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.1855+6558G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177530363 | ||||||
| chr2:177530700
|
T | C | 2 | a0001c0001t0003g0232a0001c0001t0003g0235 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1855+6895T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177530700 | ||||||
| chr2:177530757
|
A | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1855+6952A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177530757 | ||||||
| chr2:177530964
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0194 | 2 | HG01256.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1856-7110A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177530964 | ||||||
| chr2:177530968
|
T | A | 7 | a0001c0001t0003g0229a0001c0001t0003g0232a0001c0001t0003g0234others(4): Show | 7 | HG00642.hp2 HG01168.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1856-7106T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177530968 | ||||||
| chr2:177531289
|
A | G | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.1856-6785A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177531289 | ||||||
| chr2:177531558
|
G | A | 230 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(227): Show | 230 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.1856-6516G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177531558 | ||||||
| chr2:177531634
|
T | C | 1 | a0001c0001t0033g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1856-6440T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177531634 | ||||||
| chr2:177531753
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1856-6321A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177531753 | ||||||
| chr2:177532177
|
G | C | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1856-5897G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177532177 | ||||||
| chr2:177532743
|
G | A | 230 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(227): Show | 230 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.1856-5331G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177532743 | ||||||
| chr2:177532807
|
A | G | 5 | a0001c0001t0005g0104a0001c0001t0025g0253a0001c0001t0025g0254others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1856-5267A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177532807 | ||||||
| chr2:177532911
|
A | C | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1856-5163A>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177532911 | ||||||
| chr2:177533395
|
C | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1856-4679C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177533395 | ||||||
| chr2:177533653
|
A | G | 1 | a0001c0001t0041g0099 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1856-4421A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177533653 | ||||||
| chr2:177533751
|
A | G | 10 | a0001c0001t0005g0104a0001c0001t0005g0197a0001c0001t0005g0198others(7): Show | 10 | HG00735.hp1 HG01891.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1856-4323A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177533751 | ||||||
| chr2:177533836
|
T | C | 1 | a0001c0001t0024g0174 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1856-4238T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177533836 | ||||||
| chr2:177533878
|
G | C | 2 | a0001c0001t0003g0232a0001c0001t0003g0235 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1856-4196G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177533878 | ||||||
| chr2:177533963
|
T | G | 1 | a0001c0001t0001g0178 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1856-4111T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177533963 | ||||||
| chr2:177534059
|
G | C | 2 | a0001c0001t0017g0207a0001c0001t0017g0208 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1856-4015G>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177534059 | ||||||
| chr2:177534195
|
T | A | 150 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(147): Show | 150 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.1856-3879T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177534195 | ||||||
| chr2:177534224
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1856-3850G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177534224 | ||||||
| chr2:177534243
|
A | G | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1856-3831A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177534243 | ||||||
| chr2:177534381
|
T | A | 1 | a0001c0001t0039g0164 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1856-3693T>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177534381 | ||||||
| chr2:177534513
|
G | A | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1856-3561G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177534513 | ||||||
| chr2:177534546
|
C | T | 12 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1856-3528C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177534546 | ||||||
| chr2:177534552
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | NA18945.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1856-3522G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177534552 | ||||||
| chr2:177534827
|
G | A | 1 | a0001c0001t0003g0239 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1856-3247G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177534827 | ||||||
| chr2:177534833
|
A | G | 228 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(225): Show | 228 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.1856-3241A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177534833 | ||||||
| chr2:177534835
|
ATGATCTT others(2): Show |
A | 228 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(225): Show | 228 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.1856-3238_1856-323 others(13): Show |
AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177534835 | ||||||
| chr2:177534980
|
T | C | 1 | a0001c0004t0031g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1856-3094T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177534980 | ||||||
| chr2:177535023
|
T | C | 2 | a0001c0001t0003g0241a0001c0001t0003g0242 | 2 | HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1856-3051T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177535023 | ||||||
| chr2:177535069
|
G | A | 2 | a0001c0001t0019g0113a0001c0001t0019g0114 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1856-3005G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177535069 | ||||||
| chr2:177535082
|
C | T | 228 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(225): Show | 228 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.1856-2992C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177535082 | ||||||
| chr2:177535203
|
C | T | 3 | a0001c0001t0014g0020a0001c0001t0014g0021a0001c0001t0014g0022 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1856-2871C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177535203 | ||||||
| chr2:177535453
|
GC | G | 126 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(123): Show | 126 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.1856-2618delC | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 177535453 | |||||
| chr2:177535476
|
G | A | 126 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(123): Show | 126 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.1856-2598G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177535476 | ||||||
| chr2:177535667
|
G | A | 1 | a0001c0001t0013g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1856-2407G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177535667 | ||||||
| chr2:177535911
|
T | G | 2 | a0001c0001t0003g0241a0001c0001t0003g0242 | 2 | HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1856-2163T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177535911 | ||||||
| chr2:177536225
|
T | C | 7 | a0001c0001t0008g0216a0001c0001t0008g0217a0001c0001t0008g0218others(4): Show | 7 | HG01109.hp1 HG01243.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1856-1849T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177536225 | ||||||
| chr2:177536290
|
C | T | 5 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(2): Show | 5 | HG02027.hp1 HG02132.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1856-1784C>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177536290 | ||||||
| chr2:177536410
|
T | TA | 78 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(75): Show | 78 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1856-1651dupA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 177536410 | |||||
| chr2:177536466
|
T | G | 2 | a0001c0001t0033g0195a0001c0001t0035g0017 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1856-1608T>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177536466 | ||||||
| chr2:177536560
|
T | C | 151 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(148): Show | 151 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.1856-1514T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177536560 | ||||||
| chr2:177536811
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1856-1263T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177536811 | ||||||
| chr2:177536837
|
A | G | 4 | a0001c0001t0011g0245a0001c0001t0011g0246a0001c0001t0011g0247others(1): Show | 4 | HG02132.hp1 HG02165.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1856-1237A>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177536837 | ||||||
| chr2:177536937
|
G | T | 1 | a0001c0001t0046g0209 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1856-1137G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177536937 | ||||||
| chr2:177537000
|
T | C | 1 | a0001c0001t0024g0174 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1856-1074T>C | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177537000 | ||||||
| chr2:177537359
|
C | CA | 7 | a0001c0001t0001g0118a0001c0001t0001g0127a0001c0001t0001g0178others(4): Show | 7 | HG00639.hp2 HG01081.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1856-708dupA | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 177537359 | |||||
| chr2:177537609
|
C | G | 3 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0046g0209 | 3 | HG02886.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1856-465C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177537609 | ||||||
| chr2:177537657
|
G | T | 1 | a0001c0001t0020g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1856-417G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177537657 | ||||||
| chr2:177537679
|
G | A | 235 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(232): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.1856-395G>A | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177537679 | ||||||
| chr2:177537887
|
C | G | 12 | a0001c0002t0004g0002a0001c0002t0004g0003a0001c0002t0004g0004others(9): Show | 12 | HG02055.hp1 HG02602.hp1 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.1856-187C>G | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177537887 | ||||||
| chr2:177538058
|
G | T | 72 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(69): Show | 72 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1856-16G>T | AGPS | ENSG00000018510.18 | transcript | ENST00000264167.11 | protein_coding | 19/19 | chr2 | 177538058 |