| geneid | 83548 |
|---|---|
| ensemblid | ENSG00000136152.15 |
| hgncid | 18619 |
| symbol | COG3 |
| name | component of oligomeric golgi complex 3 |
| refseq_nuc | NM_031431.4 |
| refseq_prot | NP_113619.3 |
| ensembl_nuc | ENST00000349995.10 |
| ensembl_prot | ENSP00000258654.8 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 45464939 |
| end | 45536701 |
| strand | + |
| ver | v1.2 |
| region | chr13:45464939-45536701 |
| region5000 | chr13:45459939-45541701 |
| regionname0 | COG3_chr13_45464939_45536701 |
| regionname5000 | COG3_chr13_45459939_45541701 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 828 | 210 | 37 | 47 | 100 | 4 | 21 | 79 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0002 | 0/0 | 828 | 118 | 41 | 19 | 42 | 4 | 12 | 26 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0003 | 0/0 | 828 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0004 | 0/0 | 828 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0005 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0006 | 0/0 | 828 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0007 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0008 | 1/0 | 828 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2487 | 104 | 9 | 20 | 59 | 2 | 14 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| c0002 | 0/1 | 2487 | 100 | 27 | 26 | 40 | 2 | 4 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| c0003 | 0/0 | 2487 | 64 | 21 | 10 | 24 | 2 | 7 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| c0004 | 0/0 | 2487 | 29 | 2 | 5 | 16 | 2 | 4 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| c0005 | 0/0 | 2487 | 16 | 10 | 3 | 2 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| c0006 | 0/0 | 2487 | 8 | 8 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| c0007 | 0/0 | 2487 | 7 | 6 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| c0008 | 0/0 | 2487 | 2 | 0 | 1 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| c0009 | 0/0 | 2487 | 2 | 2 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| c0010 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| c0011 | 0/0 | 2487 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| c0012 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| c0013 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| c0014 | 0/0 | 2487 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| c0015 | 1/0 | 2487 | 1 | 0 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| c0016 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| c0017 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| c0018 | 0/0 | 2487 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| c0019 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2069 | 239 | 40 | 49 | 115 | 6 | 27 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| t0002 | 0/0 | 2069 | 71 | 27 | 11 | 24 | 2 | 7 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| t0003 | 0/0 | 2067 | 12 | 8 | 2 | 2 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| t0004 | 0/0 | 2069 | 8 | 8 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| t0005 | 0/0 | 2069 | 2 | 0 | 2 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| t0006 | 0/0 | 2069 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| t0007 | 0/0 | 2069 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| t0008 | 0/0 | 2069 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| t0009 | 0/0 | 2069 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| t0010 | 0/0 | 2069 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| t0011 | 0/0 | 2069 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| t0012 | 0/0 | 2069 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| t0013 | 0/0 | 2067 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| t0014 | 0/0 | 2069 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| t0015 | 0/0 | 2069 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0300 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2487 | 104 | 9 | 20 | 59 | 2 | 14 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0001c0002 | 0/1 | 2487 | 100 | 27 | 26 | 40 | 2 | 4 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0001c0008 | 0/0 | 2487 | 2 | 0 | 1 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0001c0010 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0001c0011 | 0/0 | 2487 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0001c0013 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0001c0014 | 0/0 | 2487 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0002c0003 | 0/0 | 2487 | 64 | 21 | 10 | 24 | 2 | 7 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0002c0004 | 0/0 | 2487 | 29 | 2 | 5 | 16 | 2 | 4 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0002c0005 | 0/0 | 2487 | 16 | 10 | 3 | 2 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0002c0007 | 0/0 | 2487 | 7 | 6 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0002c0012 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0002c0016 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0003c0006 | 0/0 | 2487 | 8 | 8 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0004c0009 | 0/0 | 2487 | 2 | 2 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0005c0019 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0006c0018 | 0/0 | 2487 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0007c0017 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0008c0015 | 1/0 | 2487 | 1 | 0 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4555 | 100 | 9 | 18 | 57 | 2 | 14 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0001c0001t0005 | 0/0 | 4555 | 2 | 0 | 2 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0001c0001t0006 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0001c0001t0008 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0001c0002t0001 | 0/1 | 4555 | 98 | 26 | 25 | 40 | 2 | 4 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0001c0002t0007 | 0/0 | 4555 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0001c0002t0009 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0001c0008t0001 | 0/0 | 4555 | 2 | 0 | 1 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0001c0010t0001 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0001c0011t0001 | 0/0 | 4555 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0001c0013t0004 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0001c0014t0001 | 0/0 | 4555 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0002c0003t0002 | 0/0 | 4555 | 64 | 21 | 10 | 24 | 2 | 7 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0002c0004t0001 | 0/0 | 4555 | 28 | 2 | 5 | 15 | 2 | 4 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0002c0004t0010 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0002c0005t0001 | 0/0 | 4555 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0002c0005t0003 | 0/0 | 4553 | 11 | 7 | 2 | 2 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0002c0005t0011 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0002c0005t0012 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0002c0005t0013 | 0/0 | 4553 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0002c0005t0014 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0002c0007t0002 | 0/0 | 4555 | 7 | 6 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0002c0012t0001 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0002c0016t0003 | 0/0 | 4553 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0003c0006t0004 | 0/0 | 4555 | 7 | 7 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0003c0006t0015 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0004c0009t0001 | 0/0 | 4555 | 2 | 2 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0005c0019t0001 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0006c0018t0001 | 0/0 | 4555 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0007c0017t0001 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| a0008c0015t0001 | 1/0 | 4555 | 1 | 0 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | copy fasta | chr13 | 45459939 | 45541701 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0001t0008g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0300 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0007g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0002t0009g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0008t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0008t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0010t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0011t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0013t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0001c0014t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0003t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0004t0010g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0005t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0005t0003g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0005t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0005t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0005t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0005t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0005t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0005t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0005t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0005t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0005t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0005t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0005t0012g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0005t0013g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0005t0014g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0007t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0007t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0007t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0007t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0007t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0007t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0007t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0012t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0002c0016t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0003c0006t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0003c0006t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0003c0006t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0003c0006t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0003c0006t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0003c0006t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0003c0006t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0003c0006t0015g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0004c0009t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0004c0009t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0005c0019t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0006c0018t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0007c0017t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| a0008c0015t0001g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | GBR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0301 | EUR | GBR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00280 | hp1 | a0002 | c0004 | t0001 | g0028 | EUR | FIN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00280 | hp2 | a0002 | c0003 | t0002 | g0172 | EUR | FIN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | FIN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00323 | hp2 | a0002 | c0003 | t0002 | g0144 | EUR | FIN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00408 | hp1 | a0002 | c0005 | t0003 | g0158 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00423 | hp1 | a0002 | c0003 | t0002 | g0162 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0284 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0307 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0317 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00597 | hp1 | a0002 | c0004 | t0010 | g0025 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00597 | hp2 | a0002 | c0003 | t0002 | g0190 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00609 | hp1 | a0002 | c0003 | t0002 | g0174 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00621 | hp1 | a0002 | c0003 | t0002 | g0170 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00639 | hp1 | a0002 | c0005 | t0003 | g0004 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00642 | hp1 | a0002 | c0004 | t0001 | g0018 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0293 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0299 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00738 | hp1 | a0001 | c0002 | t0007 | g0305 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00738 | hp2 | a0001 | c0008 | t0001 | g0121 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0304 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01069 | hp1 | a0002 | c0003 | t0002 | g0007 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0248 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0243 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01070 | hp2 | a0002 | c0003 | t0002 | g0179 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01071 | hp1 | a0002 | c0003 | t0002 | g0007 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0241 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01074 | hp2 | a0002 | c0003 | t0002 | g0235 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0247 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0298 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01109 | hp1 | a0002 | c0003 | t0002 | g0207 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01109 | hp2 | a0002 | c0003 | t0002 | g0208 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0252 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0328 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0310 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0326 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01192 | hp1 | a0002 | c0007 | t0002 | g0224 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0315 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01243 | hp1 | a0002 | c0005 | t0003 | g0004 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01256 | hp1 | a0002 | c0004 | t0001 | g0019 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0329 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01257 | hp1 | a0002 | c0004 | t0001 | g0030 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0061 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01258 | hp1 | a0002 | c0004 | t0001 | g0020 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0060 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01261 | hp1 | a0002 | c0004 | t0001 | g0034 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0316 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01361 | hp2 | a0002 | c0003 | t0002 | g0218 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0251 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01496 | hp1 | a0002 | c0003 | t0002 | g0187 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01496 | hp2 | a0002 | c0003 | t0002 | g0216 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01516 | hp1 | a0002 | c0004 | t0001 | g0014 | EUR | IBS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0242 | EUR | IBS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0264 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01891 | hp2 | a0002 | c0003 | t0002 | g0165 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0294 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0308 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01934 | hp2 | a0002 | c0003 | t0002 | g0217 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0249 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01975 | hp1 | a0002 | c0005 | t0013 | g0154 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0319 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0318 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0311 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02015 | hp1 | a0002 | c0005 | t0003 | g0159 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02015 | hp2 | a0002 | c0004 | t0001 | g0012 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02040 | hp1 | a0002 | c0003 | t0002 | g0005 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0262 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02055 | hp2 | a0002 | c0003 | t0002 | g0161 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02056 | hp2 | a0002 | c0003 | t0002 | g0181 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0291 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02074 | hp1 | a0002 | c0004 | t0001 | g0024 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0331 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02129 | hp1 | a0005 | c0019 | t0001 | g0070 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02129 | hp2 | a0002 | c0004 | t0001 | g0026 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02132 | hp1 | a0002 | c0003 | t0002 | g0167 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0265 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02145 | hp1 | a0002 | c0003 | t0002 | g0211 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0312 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02165 | hp1 | a0002 | c0004 | t0001 | g0023 | EAS | CDX | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CDX | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02257 | hp1 | a0002 | c0007 | t0002 | g0226 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02280 | hp1 | a0002 | c0003 | t0002 | g0164 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02280 | hp2 | a0002 | c0003 | t0002 | g0214 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0146 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02523 | hp1 | a0002 | c0003 | t0002 | g0186 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02572 | hp1 | a0002 | c0005 | t0003 | g0153 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02572 | hp2 | a0002 | c0007 | t0002 | g0223 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02602 | hp1 | a0002 | c0003 | t0002 | g0188 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02615 | hp1 | a0002 | c0005 | t0003 | g0152 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02615 | hp2 | a0004 | c0009 | t0001 | g0021 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02622 | hp1 | a0002 | c0003 | t0002 | g0234 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0245 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02630 | hp2 | a0003 | c0006 | t0015 | g0200 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02647 | hp1 | a0002 | c0003 | t0002 | g0231 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02647 | hp2 | a0002 | c0003 | t0002 | g0212 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0288 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02683 | hp2 | a0002 | c0003 | t0002 | g0177 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02698 | hp2 | a0002 | c0005 | t0001 | g0313 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02717 | hp1 | a0003 | c0006 | t0004 | g0197 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02717 | hp2 | a0002 | c0003 | t0002 | g0215 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02723 | hp1 | a0002 | c0005 | t0003 | g0192 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0269 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0254 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02818 | hp1 | a0002 | c0004 | t0001 | g0013 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02895 | hp2 | a0003 | c0006 | t0004 | g0196 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02896 | hp2 | a0002 | c0007 | t0002 | g0228 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02897 | hp1 | a0003 | c0006 | t0004 | g0195 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02922 | hp1 | a0002 | c0016 | t0003 | g0156 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0230 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0322 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02965 | hp2 | a0002 | c0005 | t0003 | g0155 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0147 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0229 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02976 | hp2 | a0002 | c0003 | t0002 | g0219 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03041 | hp1 | a0002 | c0007 | t0002 | g0232 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03041 | hp2 | a0002 | c0003 | t0002 | g0233 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03098 | hp1 | a0003 | c0006 | t0004 | g0198 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03098 | hp2 | a0002 | c0005 | t0003 | g0157 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03139 | hp1 | a0002 | c0005 | t0012 | g0148 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03139 | hp2 | a0001 | c0013 | t0004 | g0194 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0268 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03209 | hp2 | a0002 | c0003 | t0002 | g0222 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03225 | hp1 | a0002 | c0005 | t0014 | g0206 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03225 | hp2 | a0002 | c0007 | t0002 | g0227 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03239 | hp1 | a0001 | c0008 | t0001 | g0042 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03453 | hp1 | a0002 | c0007 | t0002 | g0225 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03453 | hp2 | a0002 | c0003 | t0002 | g0210 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03486 | hp1 | a0002 | c0003 | t0002 | g0209 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03486 | hp2 | a0003 | c0006 | t0004 | g0193 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0244 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03491 | hp1 | a0002 | c0003 | t0002 | g0175 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03492 | hp1 | a0002 | c0003 | t0002 | g0176 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03516 | hp1 | a0002 | c0004 | t0001 | g0038 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0290 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03540 | hp1 | a0002 | c0003 | t0002 | g0202 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0263 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0273 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03654 | hp1 | a0002 | c0003 | t0002 | g0236 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03669 | hp1 | a0002 | c0004 | t0001 | g0011 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03831 | hp1 | a0002 | c0003 | t0002 | g0238 | SAS | BEB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03942 | hp2 | a0002 | c0004 | t0001 | g0031 | SAS | BEB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG04184 | hp2 | a0006 | c0018 | t0001 | g0309 | SAS | BEB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG04199 | hp1 | a0002 | c0004 | t0001 | g0015 | SAS | STU | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0203 | SAS | STU | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG04204 | hp2 | a0001 | c0014 | t0001 | g0261 | SAS | STU | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG04228 | hp1 | a0001 | c0011 | t0001 | g0246 | SAS | STU | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG04228 | hp2 | a0002 | c0004 | t0001 | g0029 | SAS | STU | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0267 | AFR | YRI | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18522 | hp2 | a0002 | c0005 | t0011 | g0150 | AFR | YRI | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18612 | hp1 | a0002 | c0003 | t0002 | g0173 | EAS | CHB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18906 | hp1 | a0002 | c0003 | t0002 | g0237 | AFR | YRI | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0266 | AFR | YRI | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18939 | hp2 | a0002 | c0003 | t0002 | g0184 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18945 | hp1 | a0001 | c0010 | t0001 | g0128 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18945 | hp2 | a0002 | c0003 | t0002 | g0178 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18949 | hp1 | a0002 | c0003 | t0002 | g0166 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18950 | hp1 | a0002 | c0004 | t0001 | g0027 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18962 | hp2 | a0002 | c0003 | t0002 | g0160 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18964 | hp1 | a0002 | c0004 | t0001 | g0002 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0292 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18969 | hp2 | a0002 | c0004 | t0001 | g0002 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18971 | hp1 | a0002 | c0004 | t0001 | g0002 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18974 | hp2 | a0001 | c0001 | t0006 | g0064 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18979 | hp1 | a0002 | c0004 | t0001 | g0033 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18982 | hp2 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18984 | hp1 | a0007 | c0017 | t0001 | g0285 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18991 | hp2 | a0002 | c0003 | t0002 | g0005 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18994 | hp1 | a0002 | c0003 | t0002 | g0182 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18997 | hp2 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18998 | hp1 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18999 | hp1 | a0002 | c0004 | t0001 | g0032 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19001 | hp1 | a0001 | c0001 | t0008 | g0051 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19002 | hp2 | a0002 | c0003 | t0002 | g0006 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19010 | hp2 | a0002 | c0004 | t0001 | g0016 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19011 | hp2 | a0002 | c0003 | t0002 | g0189 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19012 | hp2 | a0002 | c0003 | t0002 | g0180 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0324 | AFR | LWK | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | LWK | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0289 | AFR | LWK | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19043 | hp2 | a0002 | c0003 | t0002 | g0240 | AFR | LWK | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0330 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19066 | hp2 | a0002 | c0003 | t0002 | g0183 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19077 | hp1 | a0002 | c0003 | t0002 | g0006 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19082 | hp1 | a0002 | c0003 | t0002 | g0171 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19085 | hp2 | a0002 | c0003 | t0002 | g0185 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19087 | hp1 | a0002 | c0004 | t0001 | g0017 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19089 | hp2 | a0002 | c0003 | t0002 | g0191 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0274 | AFR | YRI | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA19240 | hp2 | a0002 | c0003 | t0002 | g0213 | AFR | YRI | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA20129 | hp1 | a0002 | c0003 | t0002 | g0163 | AFR | ASW | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA20905 | hp1 | a0002 | c0003 | t0002 | g0168 | SAS | GIH | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | GIH | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0320 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02109 | hp1 | a0004 | c0009 | t0001 | g0022 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0277 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0321 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0302 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG02559 | hp2 | a0003 | c0006 | t0004 | g0199 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03471 | hp1 | a0001 | c0002 | t0009 | g0279 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG03471 | hp2 | a0002 | c0005 | t0003 | g0010 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG06807 | hp1 | a0002 | c0003 | t0002 | g0221 | AFR | USA | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| HG06807 | hp2 | a0002 | c0012 | t0001 | g0103 | AFR | USA | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18955 | hp1 | a0002 | c0003 | t0002 | g0169 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA20300 | hp1 | a0002 | c0005 | t0003 | g0151 | AFR | USA | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0327 | AFR | USA | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA21309 | hp1 | a0003 | c0006 | t0004 | g0201 | AFR | LWK | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| NA21309 | hp2 | a0002 | c0003 | t0002 | g0220 | AFR | LWK | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0300 | REF | REF | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| homoSapiens_grch38 | hp1 | a0008 | c0015 | t0001 | g0039 | REF | REF | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:45465143
|
C | G | 1 | a0005 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.107C>G | p.Thr36Ser | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/23 | 205/4555 | 107/2487 | 36/828 | chr13 | 45465143 | ||
| chr13:45476207
|
A | T | 1 | a0006 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.181A>T | p.Ile61Phe | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/23 | 279/4555 | 181/2487 | 61/828 | chr13 | 45476207 | ||
| chr13:45480223
|
A | G | 1 | a0004 | 2 | HG02109.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.482A>G | p.Gln161Arg | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 4/23 | 580/4555 | 482/2487 | 161/828 | chr13 | 45480223 | ||
| chr13:45486564
|
C | G | 1 | a0007 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.913C>G | p.Pro305Ala | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/23 | 1011/4555 | 913/2487 | 305/828 | chr13 | 45486564 | ||
| chr13:45529800
|
A | G | 5 | a0001a0003a0005others(2): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
missense_variant | MODERATE | c.2240A>G | p.Asn747Ser | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/23 | 2338/4555 | 2240/2487 | 747/828 | chr13 | 45529800 | ||
| chr13:45534718
|
T | C | 7 | a0001a0002a0003others(4): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
missense_variant | MODERATE | c.2474T>C | p.Leu825Ser | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 2572/4555 | 2474/2487 | 825/828 | chr13 | 45534718 | ||
| chr13:45534721
|
T | C | 1 | a0003 | 8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
missense_variant | MODERATE | c.2477T>C | p.Val826Ala | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 2575/4555 | 2477/2487 | 826/828 | chr13 | 45534721 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:45481232
|
G | A | 1 | a0001c0010 | 1 | NA18945.hp1 | splice_region_variant&synonymous_variant | LOW | c.552G>A | p.Ser184Ser | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 5/23 | 650/4555 | 552/2487 | 184/828 | chr13 | 45481232 | ||
| chr13:45493417
|
T | C | 1 | a0001c0011 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.1258T>C | p.Leu420Leu | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/23 | 1356/4555 | 1258/2487 | 420/828 | chr13 | 45493417 | ||
| chr13:45493458
|
G | A | 5 | a0001c0001a0001c0008a0001c0010others(2): Show | 109 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(106): Show |
synonymous_variant | LOW | c.1299G>A | p.Glu433Glu | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/23 | 1397/4555 | 1299/2487 | 433/828 | chr13 | 45493458 | ||
| chr13:45496234
|
C | T | 1 | a0002c0016 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.1410C>T | p.Ile470Ile | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/23 | 1508/4555 | 1410/2487 | 470/828 | chr13 | 45496234 | ||
| chr13:45503246
|
G | A | 16 | a0001c0001a0001c0002a0001c0008others(13): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(307): Show |
splice_region_variant&synonymous_variant | LOW | c.1491G>A | p.Gln497Gln | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/23 | 1589/4555 | 1491/2487 | 497/828 | chr13 | 45503246 | ||
| chr13:45529891
|
C | T | 1 | a0001c0014 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.2331C>T | p.Thr777Thr | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/23 | 2429/4555 | 2331/2487 | 777/828 | chr13 | 45529891 | ||
| chr13:45530714
|
C | T | 2 | a0001c0008a0002c0007 | 9 | HG00738.hp2 HG01192.hp1 HG02257.hp1 others(6): Show |
synonymous_variant | LOW | c.2391C>T | p.His797His | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/23 | 2489/4555 | 2391/2487 | 797/828 | chr13 | 45530714 | ||
| chr13:45534719
|
G | A | 11 | a0001c0001a0001c0002a0001c0008others(8): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
synonymous_variant | LOW | c.2475G>A | p.Leu825Leu | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 2573/4555 | 2475/2487 | 825/828 | chr13 | 45534719 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:45464993
|
T | C | 1 | a0001c0001t0006 | 1 | NA18974.hp2 | 5_prime_UTR_variant | MODIFIER | c.-44T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/23 | 44 | chr13 | 45464993 | |||||
| chr13:45534829
|
G | A | 1 | a0001c0002t0007 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*98G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 98 | chr13 | 45534829 | |||||
| chr13:45534891
|
T | A | 2 | a0002c0003t0002a0002c0007t0002 | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*160T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 160 | chr13 | 45534891 | |||||
| chr13:45534899
|
G | T | 1 | a0003c0006t0015 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*168G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 168 | chr13 | 45534899 | |||||
| chr13:45535057
|
T | G | 1 | a0001c0001t0005 | 2 | HG01257.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*326T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 326 | chr13 | 45535057 | |||||
| chr13:45535237
|
T | C | 1 | a0001c0001t0008 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*506T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 506 | chr13 | 45535237 | |||||
| chr13:45535308
|
T | C | 1 | a0001c0002t0009 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*577T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 577 | chr13 | 45535308 | |||||
| chr13:45535532
|
G | A | 1 | a0002c0004t0010 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*801G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 801 | chr13 | 45535532 | |||||
| chr13:45535546
|
T | C | 2 | a0002c0005t0011a0002c0005t0012 | 2 | HG03139.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*815T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 815 | chr13 | 45535546 | |||||
| chr13:45536023
|
C | A | 1 | a0002c0005t0013 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1292C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 1292 | chr13 | 45536023 | |||||
| chr13:45536105
|
ACT | A | 3 | a0002c0005t0003a0002c0005t0013a0002c0016t0003 | 13 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1379_*1380delCT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 1379 | INFO_REALIGN_3_PRIME | chr13 | 45536105 | ||||
| chr13:45536241
|
G | T | 1 | a0002c0005t0012 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1510G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 1510 | chr13 | 45536241 | |||||
| chr13:45536249
|
T | C | 3 | a0001c0013t0004a0003c0006t0004a0003c0006t0015 | 9 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1518T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 1518 | chr13 | 45536249 | |||||
| chr13:45536487
|
A | T | 1 | a0002c0005t0014 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1756A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 1756 | chr13 | 45536487 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:45465272
|
G | T | 93 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0241others(90): Show | 95 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.174+62G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45465272 | ||||||
| chr13:45465363
|
C | T | 1 | a0002c0003t0002g0240 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.174+153C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45465363 | ||||||
| chr13:45465412
|
C | A | 1 | a0002c0005t0003g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.174+202C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45465412 | ||||||
| chr13:45465651
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.174+441C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45465651 | ||||||
| chr13:45465674
|
G | T | 1 | a0002c0003t0002g0238 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.174+464G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45465674 | ||||||
| chr13:45465726
|
G | C | 30 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037others(27): Show | 34 | HG00280.hp1 HG00597.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.174+516G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45465726 | ||||||
| chr13:45465814
|
A | G | 34 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(31): Show | 35 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.174+604A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45465814 | ||||||
| chr13:45466024
|
C | A | 1 | a0001c0002t0001g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.174+814C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45466024 | ||||||
| chr13:45466072
|
C | G | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.174+862C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45466072 | ||||||
| chr13:45466109
|
C | T | 1 | a0001c0002t0001g0205 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.174+899C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45466109 | ||||||
| chr13:45466222
|
A | G | 6 | a0002c0003t0002g0233a0002c0003t0002g0234a0002c0003t0002g0235others(3): Show | 6 | HG01074.hp2 HG02622.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.174+1012A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45466222 | ||||||
| chr13:45466256
|
C | T | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.174+1046C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45466256 | ||||||
| chr13:45466328
|
C | T | 1 | a0001c0002t0001g0331 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.174+1118C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45466328 | ||||||
| chr13:45466528
|
G | T | 1 | a0002c0007t0002g0232 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.174+1318G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45466528 | ||||||
| chr13:45466687
|
A | G | 95 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(92): Show | 97 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.174+1477A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45466687 | ||||||
| chr13:45466760
|
C | T | 1 | a0002c0003t0002g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.174+1550C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45466760 | ||||||
| chr13:45467160
|
C | T | 219 | a0001c0001t0001g0149a0001c0002t0001g0008a0001c0002t0001g0009others(216): Show | 229 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.174+1950C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467160 | ||||||
| chr13:45467217
|
G | A | 1 | a0002c0004t0001g0011 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.174+2007G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467217 | ||||||
| chr13:45467221
|
A | G | 219 | a0001c0001t0001g0149a0001c0002t0001g0008a0001c0002t0001g0009others(216): Show | 229 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.174+2011A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467221 | ||||||
| chr13:45467267
|
C | T | 36 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(33): Show | 37 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.174+2057C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467267 | ||||||
| chr13:45467362
|
C | A | 50 | a0001c0001t0001g0149a0002c0003t0002g0005a0002c0003t0002g0006others(47): Show | 53 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.174+2152C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467362 | ||||||
| chr13:45467366
|
A | C | 39 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037others(36): Show | 40 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.174+2156A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467366 | ||||||
| chr13:45467516
|
C | T | 221 | a0001c0001t0001g0149a0001c0002t0001g0008a0001c0002t0001g0009others(218): Show | 231 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.174+2306C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467516 | ||||||
| chr13:45467517
|
A | G | 221 | a0001c0001t0001g0149a0001c0002t0001g0008a0001c0002t0001g0009others(218): Show | 231 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.174+2307A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467517 | ||||||
| chr13:45467519
|
A | G | 221 | a0001c0001t0001g0149a0001c0002t0001g0008a0001c0002t0001g0009others(218): Show | 231 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.174+2309A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467519 | ||||||
| chr13:45467556
|
C | T | 2 | a0002c0005t0003g0010a0002c0005t0003g0192 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.174+2346C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467556 | ||||||
| chr13:45467597
|
A | AAAAAG | 36 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(33): Show | 37 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.174+2389_174+2390i others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45467597 | |||||
| chr13:45467647
|
A | G | 50 | a0001c0001t0001g0149a0002c0003t0002g0005a0002c0003t0002g0006others(47): Show | 53 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.174+2437A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467647 | ||||||
| chr13:45467755
|
C | T | 30 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037others(27): Show | 34 | HG00280.hp1 HG00597.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.174+2545C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467755 | ||||||
| chr13:45468071
|
G | T | 43 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0160others(40): Show | 46 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.174+2861G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45468071 | ||||||
| chr13:45468349
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.174+3139C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45468349 | ||||||
| chr13:45468686
|
GA | G | 30 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037others(27): Show | 34 | HG00280.hp1 HG00597.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.174+3478delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45468686 | |||||
| chr13:45468863
|
C | T | 50 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(47): Show | 53 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.174+3653C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45468863 | ||||||
| chr13:45468894
|
A | G | 1 | a0002c0003t0002g0237 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.174+3684A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45468894 | ||||||
| chr13:45469004
|
T | C | 3 | a0001c0002t0001g0008a0001c0002t0001g0242a0001c0002t0001g0243 | 4 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+3794T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45469004 | ||||||
| chr13:45469232
|
C | G | 2 | a0001c0002t0001g0146a0001c0002t0001g0147 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.174+4022C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45469232 | ||||||
| chr13:45469245
|
CAT | C | 3 | a0001c0002t0001g0204a0001c0002t0001g0329a0001c0002t0001g0330 | 3 | HG01256.hp2 NA19064.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.174+4038_174+4039d others(4): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45469245 | |||||
| chr13:45469250
|
C | T | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG02071.hp1 NA18977.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+4040C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45469250 | ||||||
| chr13:45469332
|
G | A | 2 | a0001c0002t0001g0035a0001c0002t0001g0036 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.174+4122G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45469332 | ||||||
| chr13:45469372
|
T | C | 2 | a0002c0005t0003g0010a0002c0005t0003g0192 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.174+4162T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45469372 | ||||||
| chr13:45469459
|
A | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.174+4249A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45469459 | ||||||
| chr13:45469961
|
T | C | 1 | a0001c0002t0001g0244 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.174+4751T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45469961 | ||||||
| chr13:45470067
|
C | G | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.174+4857C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45470067 | ||||||
| chr13:45470215
|
A | G | 1 | a0002c0005t0013g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.174+5005A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45470215 | ||||||
| chr13:45470703
|
A | G | 2 | a0002c0005t0003g0010a0002c0005t0003g0192 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.174+5493A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45470703 | ||||||
| chr13:45470739
|
G | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(107): Show | 111 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.175-5462G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45470739 | ||||||
| chr13:45470817
|
T | G | 1 | a0001c0002t0001g0035 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.175-5384T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45470817 | ||||||
| chr13:45470869
|
A | G | 1 | a0001c0001t0001g0239 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175-5332A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45470869 | ||||||
| chr13:45470926
|
C | T | 300 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(297): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.175-5275C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45470926 | ||||||
| chr13:45470952
|
C | T | 36 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(33): Show | 38 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.175-5249C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45470952 | ||||||
| chr13:45470996
|
A | T | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.175-5205A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45470996 | ||||||
| chr13:45471123
|
G | T | 2 | a0001c0002t0001g0327a0001c0002t0001g0328 | 2 | HG01169.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.175-5078G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45471123 | ||||||
| chr13:45471242
|
GA | G | 215 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.175-4949delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45471242 | |||||
| chr13:45471246
|
A | T | 40 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(37): Show | 42 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.175-4955A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45471246 | ||||||
| chr13:45471683
|
T | A | 111 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(108): Show | 112 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.175-4518T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45471683 | ||||||
| chr13:45471687
|
TGTA | T | 3 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0231 | 3 | HG02647.hp1 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.175-4510_175-4508d others(5): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45471687 | |||||
| chr13:45471720
|
A | G | 2 | a0001c0002t0001g0035a0001c0002t0001g0036 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.175-4481A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45471720 | ||||||
| chr13:45471727
|
G | GT | 188 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0044others(185): Show | 193 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.175-4464dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45471727 | |||||
| chr13:45471754
|
C | T | 1 | a0002c0005t0003g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.175-4447C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45471754 | ||||||
| chr13:45471881
|
C | T | 7 | a0002c0007t0002g0223a0002c0007t0002g0224a0002c0007t0002g0225others(4): Show | 7 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.175-4320C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45471881 | ||||||
| chr13:45471930
|
G | A | 215 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.175-4271G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45471930 | ||||||
| chr13:45471946
|
T | G | 1 | a0001c0002t0001g0245 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.175-4255T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45471946 | ||||||
| chr13:45471991
|
C | T | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.175-4210C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45471991 | ||||||
| chr13:45472105
|
T | C | 1 | a0001c0002t0001g0331 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.175-4096T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45472105 | ||||||
| chr13:45472106
|
G | T | 1 | a0001c0002t0001g0331 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.175-4095G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45472106 | ||||||
| chr13:45472107
|
A | T | 1 | a0001c0002t0001g0331 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.175-4094A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45472107 | ||||||
| chr13:45472148
|
A | G | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.175-4053A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45472148 | ||||||
| chr13:45472498
|
A | G | 1 | a0002c0003t0002g0191 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.175-3703A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45472498 | ||||||
| chr13:45472705
|
C | T | 3 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007 | 4 | HG01069.hp1 HG01071.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-3496C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45472705 | ||||||
| chr13:45472746
|
C | T | 30 | a0002c0003t0002g0202a0002c0003t0002g0208a0002c0003t0002g0209others(27): Show | 30 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.175-3455C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45472746 | ||||||
| chr13:45472893
|
G | A | 1 | a0001c0011t0001g0246 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.175-3308G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45472893 | ||||||
| chr13:45473015
|
G | A | 5 | a0001c0002t0001g0247a0001c0002t0001g0248a0001c0002t0001g0249others(2): Show | 5 | HG01069.hp2 HG01081.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.175-3186G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45473015 | ||||||
| chr13:45473026
|
C | T | 50 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(47): Show | 53 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.175-3175C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45473026 | ||||||
| chr13:45473114
|
C | T | 1 | a0002c0003t0002g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.175-3087C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45473114 | ||||||
| chr13:45473314
|
A | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01243.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.175-2887A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45473314 | ||||||
| chr13:45473364
|
A | G | 300 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(297): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.175-2837A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45473364 | ||||||
| chr13:45473408
|
C | T | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.175-2793C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45473408 | ||||||
| chr13:45473949
|
G | T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.175-2252G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45473949 | ||||||
| chr13:45473965
|
A | G | 1 | a0002c0003t0002g0207 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.175-2236A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45473965 | ||||||
| chr13:45474151
|
C | CT | 9 | a0002c0003t0002g0233a0002c0004t0001g0032a0002c0004t0001g0033others(6): Show | 9 | HG01261.hp1 HG02257.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.175-2026dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45474151 | |||||
| chr13:45474151
|
C | CTCT | 9 | a0002c0003t0002g0208a0002c0003t0002g0209a0002c0003t0002g0210others(6): Show | 9 | HG01109.hp2 HG02145.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.175-2049_175-2048i others(5): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45474151 | |||||
| chr13:45474151
|
C | CTT | 8 | a0001c0002t0001g0229a0002c0003t0002g0163a0002c0003t0002g0164others(5): Show | 8 | HG01074.hp2 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.175-2027_175-2026d others(4): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45474151 | |||||
| chr13:45474151
|
C | CTTT | 51 | a0001c0002t0001g0230a0002c0003t0002g0005a0002c0003t0002g0006others(48): Show | 54 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.175-2028_175-2026d others(5): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45474151 | |||||
| chr13:45474151
|
CTTTTT | C | 208 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(205): Show | 212 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.175-2030_175-2026d others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45474151 | |||||
| chr13:45474151
|
CTTTTTT | C | 6 | a0001c0002t0001g0252a0001c0002t0001g0253a0001c0002t0001g0254others(3): Show | 6 | HG01167.hp1 HG01256.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-2031_175-2026d others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45474151 | |||||
| chr13:45474188
|
C | T | 2 | a0002c0004t0001g0031a0002c0004t0001g0034 | 2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.175-2013C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474188 | ||||||
| chr13:45474220
|
C | T | 5 | a0001c0002t0001g0324a0002c0005t0003g0157a0002c0005t0003g0158others(2): Show | 5 | HG00408.hp1 HG02015.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.175-1981C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474220 | ||||||
| chr13:45474286
|
T | G | 1 | a0001c0002t0001g0256 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.175-1915T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474286 | ||||||
| chr13:45474332
|
T | G | 7 | a0001c0001t0001g0043a0001c0002t0001g0205a0001c0002t0001g0257others(4): Show | 7 | NA18906.hp1 NA18942.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.175-1869T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474332 | ||||||
| chr13:45474361
|
A | G | 2 | a0002c0005t0003g0158a0002c0005t0003g0159 | 2 | HG00408.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.175-1840A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474361 | ||||||
| chr13:45474414
|
A | G | 301 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(298): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.175-1787A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474414 | ||||||
| chr13:45474433
|
A | T | 1 | a0001c0002t0001g0245 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.175-1768A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474433 | ||||||
| chr13:45474437
|
C | T | 1 | a0002c0004t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.175-1764C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474437 | ||||||
| chr13:45474478
|
A | G | 50 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(47): Show | 53 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.175-1723A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474478 | ||||||
| chr13:45474484
|
A | G | 300 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(297): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.175-1717A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474484 | ||||||
| chr13:45474576
|
A | G | 2 | a0002c0003t0002g0189a0002c0003t0002g0190 | 2 | HG00597.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.175-1625A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474576 | ||||||
| chr13:45474784
|
A | AC | 34 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(31): Show | 35 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.175-1416dupC | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45474784 | |||||
| chr13:45474825
|
T | A | 4 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(1): Show | 5 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.175-1376T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474825 | ||||||
| chr13:45474864
|
T | G | 206 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(203): Show | 209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.175-1337T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474864 | ||||||
| chr13:45474946
|
A | AGTCT | 300 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(297): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.175-1252_175-1249d others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45474946 | |||||
| chr13:45475003
|
G | A | 4 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-1198G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45475003 | ||||||
| chr13:45475232
|
C | T | 215 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.175-969C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45475232 | ||||||
| chr13:45475280
|
C | T | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.175-921C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45475280 | ||||||
| chr13:45475402
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.175-799C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45475402 | ||||||
| chr13:45475483
|
C | T | 1 | a0001c0002t0001g0323 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.175-718C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45475483 | ||||||
| chr13:45475492
|
C | T | 1 | a0001c0002t0001g0326 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.175-709C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45475492 | ||||||
| chr13:45475505
|
T | C | 1 | a0002c0003t0002g0208 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.175-696T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45475505 | ||||||
| chr13:45475575
|
A | G | 1 | a0002c0003t0002g0240 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.175-626A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45475575 | ||||||
| chr13:45475964
|
CA | C | 50 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(47): Show | 53 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.175-222delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45475964 | |||||
| chr13:45476384
|
T | C | 111 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(108): Show | 112 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.321+37T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45476384 | ||||||
| chr13:45476523
|
A | G | 46 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(43): Show | 49 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.321+176A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45476523 | ||||||
| chr13:45476610
|
T | C | 40 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(37): Show | 42 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.321+263T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45476610 | ||||||
| chr13:45476711
|
T | TA | 219 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.321+370dupA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 45476711 | |||||
| chr13:45476712
|
A | T | 2 | a0002c0005t0003g0010a0002c0005t0003g0192 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.321+365A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45476712 | ||||||
| chr13:45476748
|
A | G | 1 | a0001c0002t0001g0322 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.321+401A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45476748 | ||||||
| chr13:45476916
|
G | A | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.321+569G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45476916 | ||||||
| chr13:45477144
|
C | T | 2 | a0002c0003t0002g0006a0002c0003t0002g0162 | 3 | HG00423.hp1 NA19002.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.321+797C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477144 | ||||||
| chr13:45477152
|
C | T | 2 | a0001c0002t0001g0146a0001c0002t0001g0147 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.321+805C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477152 | ||||||
| chr13:45477238
|
T | C | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.321+891T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477238 | ||||||
| chr13:45477259
|
G | C | 1 | a0001c0002t0001g0322 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.321+912G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477259 | ||||||
| chr13:45477453
|
T | C | 1 | a0001c0013t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.321+1106T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477453 | ||||||
| chr13:45477619
|
A | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG00558.hp1 NA18949.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.321+1272A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477619 | ||||||
| chr13:45477631
|
C | CT | 84 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0005others(81): Show | 88 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.321+1298dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 45477631 | |||||
| chr13:45477632
|
T | A | 1 | a0001c0014t0001g0261 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.321+1285T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477632 | ||||||
| chr13:45477906
|
G | A | 1 | a0001c0002t0001g0331 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.322-1099G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477906 | ||||||
| chr13:45477916
|
A | G | 215 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.322-1089A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477916 | ||||||
| chr13:45477955
|
A | C | 4 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(1): Show | 5 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-1050A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477955 | ||||||
| chr13:45477999
|
G | A | 215 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.322-1006G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477999 | ||||||
| chr13:45478196
|
CT | C | 215 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.322-796delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 45478196 | |||||
| chr13:45478214
|
C | T | 215 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.322-791C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478214 | ||||||
| chr13:45478261
|
G | A | 21 | a0002c0003t0002g0208a0002c0003t0002g0209a0002c0003t0002g0210others(18): Show | 21 | HG01074.hp2 HG01109.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.322-744G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478261 | ||||||
| chr13:45478303
|
C | T | 7 | a0002c0007t0002g0223a0002c0007t0002g0224a0002c0007t0002g0225others(4): Show | 7 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.322-702C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478303 | ||||||
| chr13:45478402
|
A | G | 2 | a0002c0005t0003g0004a0002c0005t0003g0155 | 3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.322-603A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478402 | ||||||
| chr13:45478470
|
C | T | 1 | a0002c0003t0002g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.322-535C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478470 | ||||||
| chr13:45478479
|
T | A | 1 | a0001c0001t0001g0139 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.322-526T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478479 | ||||||
| chr13:45478546
|
C | T | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.322-459C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478546 | ||||||
| chr13:45478551
|
T | G | 1 | a0001c0002t0001g0262 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.322-454T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478551 | ||||||
| chr13:45478592
|
A | G | 300 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(297): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.322-413A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478592 | ||||||
| chr13:45478645
|
C | T | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.322-360C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478645 | ||||||
| chr13:45478649
|
T | C | 300 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(297): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.322-356T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478649 | ||||||
| chr13:45478732
|
G | A | 1 | a0002c0003t0002g0207 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.322-273G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478732 | ||||||
| chr13:45478749
|
A | G | 1 | a0002c0004t0001g0029 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.322-256A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478749 | ||||||
| chr13:45478797
|
G | A | 21 | a0002c0003t0002g0208a0002c0003t0002g0209a0002c0003t0002g0210others(18): Show | 21 | HG01074.hp2 HG01109.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.322-208G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478797 | ||||||
| chr13:45479385
|
A | AGGAGAAA others(25): Show |
1 | a0001c0002t0001g0321 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.383+320_383+351dup others(32): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr13 | 45479385 | |||||
| chr13:45479409
|
T | G | 50 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(47): Show | 53 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.383+343T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 3/22 | chr13 | 45479409 | ||||||
| chr13:45479414
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.383+348A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 3/22 | chr13 | 45479414 | ||||||
| chr13:45479458
|
C | T | 300 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(297): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.383+392C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 3/22 | chr13 | 45479458 | ||||||
| chr13:45479603
|
G | A | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.384-522G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 3/22 | chr13 | 45479603 | ||||||
| chr13:45480489
|
G | A | 1 | a0002c0004t0001g0030 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.549+199G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 4/22 | chr13 | 45480489 | ||||||
| chr13:45480534
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.549+244A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 4/22 | chr13 | 45480534 | ||||||
| chr13:45480668
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0145 | 2 | HG02165.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.549+378C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 4/22 | chr13 | 45480668 | ||||||
| chr13:45480765
|
C | T | 3 | a0001c0002t0001g0318a0001c0002t0001g0319a0001c0002t0001g0320 | 3 | HG01123.hp2 HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.550-465C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 4/22 | chr13 | 45480765 | ||||||
| chr13:45480918
|
A | C | 1 | a0001c0010t0001g0128 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.550-312A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 4/22 | chr13 | 45480918 | ||||||
| chr13:45481068
|
T | A | 1 | a0001c0001t0001g0044 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.550-162T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 4/22 | chr13 | 45481068 | ||||||
| chr13:45481090
|
G | A | 9 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(6): Show | 9 | HG00544.hp2 HG00621.hp2 NA18970.hp2 others(6): Show |
intron_variant | MODIFIER | c.550-140G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 4/22 | chr13 | 45481090 | ||||||
| chr13:45481342
|
T | A | 2 | a0002c0005t0011g0150a0002c0005t0012g0148 | 2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.624+38T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 5/22 | chr13 | 45481342 | ||||||
| chr13:45481660
|
T | C | 44 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(41): Show | 47 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.624+356T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 5/22 | chr13 | 45481660 | ||||||
| chr13:45481798
|
A | G | 1 | a0001c0002t0001g0317 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.624+494A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 5/22 | chr13 | 45481798 | ||||||
| chr13:45481837
|
AG | A | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.624+534delG | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 5/22 | chr13 | 45481837 | ||||||
| chr13:45482125
|
A | G | 1 | a0001c0002t0001g0251 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.625-256A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 5/22 | chr13 | 45482125 | ||||||
| chr13:45482213
|
C | T | 111 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(108): Show | 112 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.625-168C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 5/22 | chr13 | 45482213 | ||||||
| chr13:45482245
|
A | G | 1 | a0002c0003t0002g0215 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.625-136A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 5/22 | chr13 | 45482245 | ||||||
| chr13:45482348
|
A | G | 4 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(1): Show | 5 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.625-33A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 5/22 | chr13 | 45482348 | ||||||
| chr13:45482674
|
T | A | 1 | a0001c0002t0001g0245 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.717+201T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 6/22 | chr13 | 45482674 | ||||||
| chr13:45482778
|
C | T | 50 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(47): Show | 53 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.717+305C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 6/22 | chr13 | 45482778 | ||||||
| chr13:45482816
|
T | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(107): Show | 111 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.717+343T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 6/22 | chr13 | 45482816 | ||||||
| chr13:45482852
|
A | G | 3 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007 | 4 | HG01069.hp1 HG01071.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.718-378A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 6/22 | chr13 | 45482852 | ||||||
| chr13:45483020
|
G | T | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.718-210G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 6/22 | chr13 | 45483020 | ||||||
| chr13:45483071
|
T | C | 1 | a0001c0002t0001g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.718-159T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 6/22 | chr13 | 45483071 | ||||||
| chr13:45483151
|
G | A | 50 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(47): Show | 53 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.718-79G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 6/22 | chr13 | 45483151 | ||||||
| chr13:45483374
|
A | G | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.843+19A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45483374 | ||||||
| chr13:45483422
|
A | C | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.843+67A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45483422 | ||||||
| chr13:45483522
|
A | G | 6 | a0002c0003t0002g0233a0002c0003t0002g0234a0002c0003t0002g0235others(3): Show | 6 | HG01074.hp2 HG02622.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.843+167A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45483522 | ||||||
| chr13:45483584
|
C | T | 53 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044others(50): Show | 53 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.843+229C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45483584 | ||||||
| chr13:45483633
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.843+278A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45483633 | ||||||
| chr13:45483637
|
C | T | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.843+282C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45483637 | ||||||
| chr13:45483876
|
A | C | 8 | a0003c0006t0004g0193a0003c0006t0004g0195a0003c0006t0004g0196others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.843+521A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45483876 | ||||||
| chr13:45484176
|
T | G | 34 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(31): Show | 35 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.843+821T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45484176 | ||||||
| chr13:45484234
|
T | A | 9 | a0001c0002t0001g0264a0002c0003t0002g0216a0002c0007t0002g0223others(6): Show | 9 | HG01192.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.843+879T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45484234 | ||||||
| chr13:45484371
|
GAGGGATG others(7): Show |
G | 109 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(106): Show | 110 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.843+1017_843+1030d others(16): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45484371 | ||||||
| chr13:45484460
|
A | G | 1 | a0001c0002t0001g0147 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.843+1105A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45484460 | ||||||
| chr13:45484513
|
A | G | 1 | a0002c0003t0002g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.843+1158A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45484513 | ||||||
| chr13:45484574
|
TTGCTTAT others(3): Show |
T | 34 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(31): Show | 35 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.843+1221_843+1230d others(12): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45484574 | |||||
| chr13:45484577
|
CTTAT | C | 18 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0140others(15): Show | 19 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.843+1257_843+1260d others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45484577 | |||||
| chr13:45484577
|
CTTATTTA others(1): Show |
C | 213 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(210): Show | 216 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.843+1253_843+1260d others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45484577 | |||||
| chr13:45484608
|
A | T | 1 | a0002c0004t0001g0028 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.843+1253A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45484608 | ||||||
| chr13:45484683
|
G | A | 40 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(37): Show | 42 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.843+1328G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45484683 | ||||||
| chr13:45484807
|
C | G | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.843+1452C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45484807 | ||||||
| chr13:45484856
|
C | A | 95 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(92): Show | 97 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.843+1501C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45484856 | ||||||
| chr13:45484873
|
C | T | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.843+1518C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45484873 | ||||||
| chr13:45485001
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.844-1494C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485001 | ||||||
| chr13:45485005
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.844-1490C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485005 | ||||||
| chr13:45485013
|
C | T | 2 | a0002c0005t0011g0150a0002c0005t0012g0148 | 2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.844-1482C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485013 | ||||||
| chr13:45485076
|
T | C | 265 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(262): Show | 271 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.844-1419T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485076 | ||||||
| chr13:45485158
|
C | T | 2 | a0002c0005t0003g0158a0002c0005t0003g0159 | 2 | HG00408.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.844-1337C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485158 | ||||||
| chr13:45485176
|
G | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | NA18984.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.844-1319G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485176 | ||||||
| chr13:45485178
|
C | T | 214 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(211): Show | 217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.844-1317C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485178 | ||||||
| chr13:45485191
|
C | T | 215 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.844-1304C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485191 | ||||||
| chr13:45485224
|
A | C | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.844-1271A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485224 | ||||||
| chr13:45485224
|
A | G | 34 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(31): Show | 35 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.844-1271A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485224 | ||||||
| chr13:45485228
|
G | A | 2 | a0001c0002t0001g0146a0001c0002t0001g0147 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.844-1267G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485228 | ||||||
| chr13:45485242
|
C | G | 47 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(44): Show | 50 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.844-1253C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485242 | ||||||
| chr13:45485257
|
T | C | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-1238T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485257 | ||||||
| chr13:45485270
|
C | T | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.844-1225C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485270 | ||||||
| chr13:45485284
|
A | AC | 33 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(30): Show | 34 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.844-1211_844-1210i others(3): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485284 | ||||||
| chr13:45485285
|
A | C | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-1210A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485285 | ||||||
| chr13:45485307
|
A | G | 300 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(297): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.844-1188A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485307 | ||||||
| chr13:45485311
|
C | T | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.844-1184C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485311 | ||||||
| chr13:45485312
|
A | G | 300 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(297): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.844-1183A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485312 | ||||||
| chr13:45485319
|
T | C | 146 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(143): Show | 148 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.844-1176T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485319 | ||||||
| chr13:45485381
|
G | A | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-1114G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485381 | ||||||
| chr13:45485384
|
C | CGGGGCGG others(772): Show |
1 | a0002c0004t0001g0033 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(781): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485384 | |||||
| chr13:45485384
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.844-1111C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485384 | ||||||
| chr13:45485389
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.844-1106C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485389 | ||||||
| chr13:45485401
|
C | G | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-1094C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485401 | ||||||
| chr13:45485402
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.844-1093G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485402 | ||||||
| chr13:45485402
|
G | GGAGGGCT others(365): Show |
1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.844-1092_844-1091i others(374): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | |||||
| chr13:45485402
|
G | GGAGGGCT others(365): Show |
1 | a0002c0003t0002g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.844-1092_844-1091i others(374): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | |||||
| chr13:45485402
|
G | GGAGGGCT others(365): Show |
24 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(21): Show | 25 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.844-1092_844-1091i others(374): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | |||||
| chr13:45485402
|
G | GGAGGGCT others(365): Show |
3 | a0002c0003t0002g0218a0002c0003t0002g0219a0002c0003t0002g0220 | 3 | HG01361.hp2 HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.844-1092_844-1091i others(374): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | |||||
| chr13:45485402
|
G | GGAGGGCT others(316): Show |
2 | a0002c0003t0002g0213a0002c0003t0002g0214 | 2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.844-1092_844-1091i others(325): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | |||||
| chr13:45485402
|
G | GGAGGGCT others(366): Show |
1 | a0002c0003t0002g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.844-1092_844-1091i others(375): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | |||||
| chr13:45485402
|
G | GGAGGGCT others(368): Show |
1 | a0002c0003t0002g0208 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.844-1092_844-1091i others(377): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | |||||
| chr13:45485402
|
G | GGAGGGCT others(368): Show |
1 | a0002c0007t0002g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.844-1092_844-1091i others(377): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | |||||
| chr13:45485402
|
G | GGAGGGCT others(369): Show |
1 | a0002c0003t0002g0238 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.844-1092_844-1091i others(378): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | |||||
| chr13:45485402
|
G | GGGGGGGC others(770): Show |
2 | a0001c0002t0001g0035a0001c0002t0001g0036 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(779): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | |||||
| chr13:45485402
|
G | GGGGGGGC others(770): Show |
1 | a0002c0004t0001g0029 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(779): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | |||||
| chr13:45485402
|
G | GGGGGGGC others(770): Show |
20 | a0002c0004t0001g0001a0002c0004t0001g0002a0002c0004t0001g0011others(17): Show | 24 | HG00280.hp1 HG00642.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.844-1056_844-1055i others(779): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | |||||
| chr13:45485402
|
G | GGGGGGGC others(770): Show |
1 | a0001c0002t0001g0037 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(779): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | |||||
| chr13:45485402
|
G | GGGGGGGC others(771): Show |
1 | a0002c0004t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(780): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | |||||
| chr13:45485402
|
G | GGGGGGGC others(771): Show |
1 | a0002c0004t0001g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(780): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | |||||
| chr13:45485402
|
G | GGGGGGGC others(771): Show |
1 | a0002c0004t0001g0024 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.844-1075_844-1074i others(780): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | |||||
| chr13:45485402
|
G | GGGGGGGG others(772): Show |
1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.844-1087_844-1086i others(781): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | |||||
| chr13:45485402
|
G | GGGGGGGG others(826): Show |
1 | a0001c0002t0001g0315 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.844-1087_844-1086i others(835): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | |||||
| chr13:45485402
|
G | GGGGGGGG others(776): Show |
1 | a0002c0004t0010g0025 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.844-1087_844-1086i others(785): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | |||||
| chr13:45485403
|
G | T | 1 | a0001c0002t0001g0316 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.844-1092G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485403 | ||||||
| chr13:45485412
|
A | AC | 14 | a0001c0001t0001g0086a0001c0002t0001g0229a0001c0002t0001g0230others(11): Show | 15 | HG01069.hp1 HG01071.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.844-1075dupC | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACACCCCC others(593): Show |
1 | a0001c0001t0001g0126 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.844-1082_844-1081i others(602): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACC | 17 | a0002c0003t0002g0210a0002c0003t0002g0211a0002c0003t0002g0212others(14): Show | 17 | HG01074.hp2 HG01361.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.844-1076_844-1075d others(4): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(773): Show |
1 | a0002c0004t0001g0034 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(821): Show |
1 | a0002c0003t0002g0167 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(821): Show |
1 | a0002c0005t0003g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(821): Show |
2 | a0002c0005t0003g0158a0002c0005t0003g0159 | 2 | HG00408.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(821): Show |
2 | a0002c0005t0003g0157a0002c0016t0003g0156 | 2 | HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(821): Show |
21 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(18): Show | 23 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(20): Show |
intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(821): Show |
1 | a0002c0003t0002g0207 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(822): Show |
1 | a0002c0003t0002g0189 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(826): Show |
1 | a0002c0003t0002g0190 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(835): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(771): Show |
4 | a0002c0005t0003g0151a0002c0005t0003g0152a0002c0005t0003g0153others(1): Show | 4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.844-1056_844-1055i others(780): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(821): Show |
1 | a0002c0005t0003g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(822): Show |
2 | a0002c0003t0002g0180a0002c0003t0002g0181 | 2 | HG02056.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(821): Show |
1 | a0002c0003t0002g0182 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(821): Show |
1 | a0002c0003t0002g0183 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(822): Show |
1 | a0002c0003t0002g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(821): Show |
9 | a0001c0013t0004g0194a0003c0006t0004g0193a0003c0006t0004g0195others(6): Show | 9 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(821): Show |
1 | a0002c0003t0002g0184 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(822): Show |
1 | a0002c0003t0002g0185 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(823): Show |
1 | a0002c0003t0002g0186 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(832): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(822): Show |
2 | a0002c0003t0002g0187a0002c0003t0002g0191 | 2 | HG01496.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(823): Show |
1 | a0002c0003t0002g0188 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(832): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(772): Show |
1 | a0001c0001t0001g0092 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(781): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(772): Show |
4 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(1): Show | 4 | NA18944.hp2 NA18969.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.844-1056_844-1055i others(781): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(674): Show |
1 | a0001c0001t0001g0054 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(683): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(821): Show |
3 | a0001c0002t0001g0266a0001c0002t0001g0267a0001c0002t0001g0322 | 3 | HG02965.hp1 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(772): Show |
1 | a0001c0001t0001g0055 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(781): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(821): Show |
73 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0204others(70): Show | 75 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(822): Show |
2 | a0001c0002t0001g0265a0001c0002t0001g0306 | 2 | HG02074.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(822): Show |
1 | a0001c0002t0001g0203 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(873): Show |
1 | a0001c0002t0001g0307 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(882): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(822): Show |
1 | a0001c0002t0001g0308 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(772): Show |
65 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0043others(62): Show | 66 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.844-1056_844-1055i others(781): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(773): Show |
5 | a0001c0001t0001g0053a0001c0001t0001g0076a0001c0001t0001g0077others(2): Show | 5 | HG02622.hp2 HG03831.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(773): Show |
1 | a0001c0001t0001g0139 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(773): Show |
1 | a0001c0001t0001g0041 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(773): Show |
1 | a0001c0001t0001g0078 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(772): Show |
1 | a0001c0001t0001g0079 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(781): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(773): Show |
1 | a0001c0001t0001g0117 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(773): Show |
1 | a0001c0001t0001g0135 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(772): Show |
1 | a0001c0001t0001g0118 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(781): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(823): Show |
1 | a0001c0002t0001g0260 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(832): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(826): Show |
1 | a0006c0018t0001g0309 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(835): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(773): Show |
1 | a0001c0001t0001g0119 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(775): Show |
1 | a0001c0001t0001g0080 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(784): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(822): Show |
1 | a0001c0002t0001g0251 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(822): Show |
3 | a0001c0002t0001g0262a0001c0002t0001g0310a0001c0002t0001g0311 | 3 | HG01175.hp1 HG01993.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(773): Show |
1 | a0001c0001t0001g0239 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(824): Show |
1 | a0001c0002t0001g0255 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(833): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(774): Show |
1 | a0001c0001t0001g0130 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(783): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(774): Show |
1 | a0001c0001t0001g0120 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(783): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(674): Show |
1 | a0001c0008t0001g0042 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(683): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(675): Show |
1 | a0001c0008t0001g0121 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(684): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(698): Show |
1 | a0001c0014t0001g0261 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(707): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(822): Show |
1 | a0001c0002t0001g0312 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(773): Show |
2 | a0001c0001t0001g0044a0001c0001t0001g0122 | 2 | HG01099.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(774): Show |
1 | a0001c0001t0001g0123 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(783): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(774): Show |
1 | a0001c0001t0001g0132 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(783): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(774): Show |
1 | a0001c0001t0001g0081 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(783): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(821): Show |
2 | a0001c0002t0001g0327a0001c0002t0001g0328 | 2 | HG01169.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(822): Show |
2 | a0001c0002t0001g0245a0002c0005t0001g0313 | 2 | HG02630.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(773): Show |
1 | a0001c0001t0001g0143 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(774): Show |
1 | a0001c0001t0001g0083 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(783): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(774): Show |
1 | a0001c0001t0001g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(783): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(822): Show |
2 | a0001c0002t0001g0146a0001c0002t0001g0147 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.844-1075_844-1074i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(773): Show |
2 | a0001c0001t0001g0084a0001c0001t0001g0124 | 2 | HG04204.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.844-1075_844-1074i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(774): Show |
1 | a0001c0001t0001g0085 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.844-1075_844-1074i others(783): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(823): Show |
1 | a0001c0002t0001g0314 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.844-1075_844-1074i others(832): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(778): Show |
1 | a0001c0001t0001g0125 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.844-1075_844-1074i others(787): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485412
|
A | ACCCCCCC others(780): Show |
1 | a0001c0001t0001g0091 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.844-1075_844-1074i others(789): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | |||||
| chr13:45485414
|
C | CCCCCCCA others(822): Show |
2 | a0002c0005t0003g0004a0002c0005t0003g0155 | 3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485414 | |||||
| chr13:45485414
|
C | CCCCCCCA others(816): Show |
1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(825): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485414 | |||||
| chr13:45485414
|
C | CCCCCCCA others(820): Show |
1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(829): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485414 | |||||
| chr13:45485435
|
C | CGGGGCGG others(773): Show |
1 | a0001c0001t0001g0082 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485435 | |||||
| chr13:45485439
|
G | GCGGCTGG others(773): Show |
1 | a0001c0001t0001g0075 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485439 | ||||||
| chr13:45485440
|
T | G | 1 | a0001c0001t0001g0075 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.844-1055T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485440 | ||||||
| chr13:45485457
|
C | T | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-1038C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485457 | ||||||
| chr13:45485516
|
G | A | 8 | a0002c0005t0014g0206a0002c0007t0002g0223a0002c0007t0002g0224others(5): Show | 8 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.844-979G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485516 | ||||||
| chr13:45485527
|
C | T | 1 | a0001c0002t0001g0315 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.844-968C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485527 | ||||||
| chr13:45485586
|
C | T | 1 | a0002c0003t0002g0207 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.844-909C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485586 | ||||||
| chr13:45485614
|
C | T | 1 | a0002c0003t0002g0237 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.844-881C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485614 | ||||||
| chr13:45485632
|
C | T | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.844-863C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485632 | ||||||
| chr13:45485636
|
G | A | 96 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(93): Show | 98 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.844-859G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485636 | ||||||
| chr13:45485648
|
CAGA | C | 9 | a0001c0013t0004g0194a0003c0006t0004g0193a0003c0006t0004g0195others(6): Show | 9 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-846_844-844del others(3): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485648 | ||||||
| chr13:45485654
|
C | T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.844-841C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485654 | ||||||
| chr13:45485729
|
ACGCTCCT others(33): Show |
A | 2 | a0002c0005t0011g0150a0002c0005t0012g0148 | 2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.844-745_844-706del others(40): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485729 | |||||
| chr13:45485818
|
A | T | 110 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(107): Show | 111 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.844-677A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485818 | ||||||
| chr13:45485851
|
C | T | 30 | a0002c0003t0002g0202a0002c0003t0002g0208a0002c0003t0002g0209others(27): Show | 30 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.844-644C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485851 | ||||||
| chr13:45485865
|
T | C | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-630T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485865 | ||||||
| chr13:45485894
|
A | G | 1 | a0001c0002t0001g0255 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.844-601A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485894 | ||||||
| chr13:45485904
|
C | CG | 8 | a0001c0001t0001g0056a0001c0001t0001g0076a0001c0001t0001g0126others(5): Show | 8 | HG01099.hp1 HG01192.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.844-587dupG | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485904 | |||||
| chr13:45485982
|
G | T | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-513G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485982 | ||||||
| chr13:45485989
|
G | A | 2 | a0001c0002t0001g0327a0001c0002t0001g0328 | 2 | HG01169.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.844-506G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485989 | ||||||
| chr13:45486060
|
G | A | 23 | a0002c0003t0002g0202a0002c0003t0002g0208a0002c0003t0002g0209others(20): Show | 23 | HG01074.hp2 HG01109.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.844-435G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486060 | ||||||
| chr13:45486067
|
C | A | 1 | a0001c0002t0001g0306 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.844-428C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486067 | ||||||
| chr13:45486068
|
G | C | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.844-427G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486068 | ||||||
| chr13:45486084
|
C | T | 50 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(47): Show | 53 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.844-411C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486084 | ||||||
| chr13:45486093
|
C | T | 9 | a0002c0005t0012g0148a0003c0006t0004g0193a0003c0006t0004g0195others(6): Show | 9 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-402C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486093 | ||||||
| chr13:45486106
|
T | C | 1 | a0002c0003t0002g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.844-389T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486106 | ||||||
| chr13:45486133
|
A | G | 48 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(45): Show | 51 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.844-362A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486133 | ||||||
| chr13:45486138
|
C | T | 215 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.844-357C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486138 | ||||||
| chr13:45486161
|
C | T | 1 | a0001c0002t0001g0147 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.844-334C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486161 | ||||||
| chr13:45486238
|
C | T | 4 | a0001c0002t0001g0203a0001c0002t0001g0331a0001c0011t0001g0246others(1): Show | 4 | HG02080.hp2 HG02698.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.844-257C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486238 | ||||||
| chr13:45486265
|
C | A | 96 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(93): Show | 98 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.844-230C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486265 | ||||||
| chr13:45486265
|
C | T | 1 | a0002c0003t0002g0189 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.844-230C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486265 | ||||||
| chr13:45486271
|
G | C | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-224G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486271 | ||||||
| chr13:45486289
|
T | TCGGGAGA | 5 | a0002c0004t0001g0011a0002c0004t0001g0029a0002c0004t0001g0030others(2): Show | 5 | HG01257.hp1 HG01261.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.844-156_844-150dup others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486289 | |||||
| chr13:45486289
|
T | TCGGGAGA others(14): Show |
1 | a0002c0004t0001g0012 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.844-170_844-150dup others(21): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486289 | |||||
| chr13:45486289
|
TCGGGAGA | T | 10 | a0001c0001t0005g0060a0001c0001t0005g0061a0002c0004t0001g0018others(7): Show | 10 | HG00597.hp1 HG00642.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.844-156_844-150del others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486289 | |||||
| chr13:45486289
|
TCGGGAGA others(7): Show |
T | 27 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0054others(24): Show | 28 | HG00639.hp1 HG01099.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.844-163_844-150del others(14): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486289 | |||||
| chr13:45486289
|
TCGGGAGA others(14): Show |
T | 52 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037others(49): Show | 54 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.844-170_844-150del others(21): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486289 | |||||
| chr13:45486290
|
C | G | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-205C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486290 | ||||||
| chr13:45486297
|
CG | C | 12 | a0002c0003t0002g0233a0002c0003t0002g0234a0002c0003t0002g0235others(9): Show | 12 | HG01074.hp2 HG01192.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.844-195delG | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486297 | |||||
| chr13:45486297
|
CGGGAGAC others(1): Show |
C | 17 | a0002c0003t0002g0202a0002c0003t0002g0208a0002c0003t0002g0209others(14): Show | 17 | HG01109.hp2 HG01361.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.844-195_844-188del others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486297 | |||||
| chr13:45486297
|
CGGGAGAC others(8): Show |
C | 5 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.844-195_844-181del others(15): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486297 | |||||
| chr13:45486297
|
CGGGAGAC others(15): Show |
C | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.844-195_844-174del others(22): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486297 | |||||
| chr13:45486303
|
AC | A | 12 | a0002c0003t0002g0233a0002c0003t0002g0234a0002c0003t0002g0235others(9): Show | 12 | HG01074.hp2 HG01192.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.844-191delC | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486303 | ||||||
| chr13:45486308
|
A | G | 7 | a0002c0007t0002g0223a0002c0007t0002g0224a0002c0007t0002g0225others(4): Show | 7 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.844-187A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486308 | ||||||
| chr13:45486310
|
AC | A | 29 | a0002c0003t0002g0202a0002c0003t0002g0208a0002c0003t0002g0209others(26): Show | 29 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.844-184delC | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486310 | ||||||
| chr13:45486315
|
A | G | 13 | a0002c0003t0002g0233a0002c0003t0002g0234a0002c0003t0002g0235others(10): Show | 13 | HG01074.hp2 HG01192.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.844-180A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486315 | ||||||
| chr13:45486317
|
AC | A | 33 | a0001c0001t0001g0076a0001c0002t0001g0229a0001c0002t0001g0230others(30): Show | 34 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.844-177delC | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486317 | ||||||
| chr13:45486318
|
C | G | 2 | a0002c0007t0002g0224a0002c0007t0002g0232 | 2 | HG01192.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.844-177C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486318 | ||||||
| chr13:45486318
|
C | T | 1 | a0001c0013t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.844-177C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486318 | ||||||
| chr13:45486322
|
A | G | 29 | a0002c0003t0002g0202a0002c0003t0002g0208a0002c0003t0002g0209others(26): Show | 29 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.844-173A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486322 | ||||||
| chr13:45486323
|
G | A | 2 | a0002c0007t0002g0224a0002c0007t0002g0232 | 2 | HG01192.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.844-172G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486323 | ||||||
| chr13:45486324
|
A | G | 2 | a0002c0007t0002g0224a0002c0007t0002g0232 | 2 | HG01192.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.844-171A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486324 | ||||||
| chr13:45486324
|
AC | A | 34 | a0001c0001t0001g0076a0001c0001t0001g0115a0001c0002t0001g0229others(31): Show | 35 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.844-170delC | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486324 | ||||||
| chr13:45486325
|
C | CGGGAGAC others(6): Show |
1 | a0002c0004t0001g0028 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.844-169_844-157dup others(13): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486325 | |||||
| chr13:45486325
|
C | G | 3 | a0002c0003t0002g0208a0002c0007t0002g0224a0002c0007t0002g0232 | 3 | HG01109.hp2 HG01192.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.844-170C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486325 | ||||||
| chr13:45486325
|
CGGGAGAC others(1): Show |
C | 3 | a0001c0002t0001g0264a0001c0002t0001g0268a0001c0014t0001g0261 | 3 | HG01891.hp1 HG03209.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.844-167_844-160del others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486325 | |||||
| chr13:45486329
|
A | G | 33 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(30): Show | 34 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.844-166A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486329 | ||||||
| chr13:45486331
|
A | G | 2 | a0002c0007t0002g0224a0002c0007t0002g0232 | 2 | HG01192.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.844-164A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486331 | ||||||
| chr13:45486331
|
AC | A | 34 | a0001c0001t0001g0076a0001c0001t0001g0115a0001c0002t0001g0229others(31): Show | 35 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.844-163delC | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486331 | ||||||
| chr13:45486332
|
C | G | 3 | a0002c0007t0002g0223a0002c0007t0002g0224a0002c0007t0002g0232 | 3 | HG01192.hp1 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.844-163C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486332 | ||||||
| chr13:45486332
|
CG | C | 63 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(60): Show | 65 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.844-160delG | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486332 | |||||
| chr13:45486332
|
CGGGAGAC others(6): Show |
C | 5 | a0003c0006t0004g0195a0003c0006t0004g0196a0003c0006t0004g0197others(2): Show | 5 | HG02559.hp2 HG02717.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.844-156_844-144del others(13): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486332 | |||||
| chr13:45486336
|
A | G | 35 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(32): Show | 36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-159A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486336 | ||||||
| chr13:45486337
|
G | A | 1 | a0002c0007t0002g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.844-158G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486337 | ||||||
| chr13:45486338
|
A | AGGGAG | 9 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0056others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.844-157_844-156ins others(5): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486338 | ||||||
| chr13:45486338
|
A | AGGGAGAG others(4): Show |
28 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0048others(25): Show | 29 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.844-157_844-156ins others(11): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486338 | ||||||
| chr13:45486338
|
A | AGGGAGAG others(10): Show |
14 | a0001c0001t0001g0052a0001c0001t0001g0069a0001c0001t0001g0075others(11): Show | 14 | HG00099.hp1 HG01981.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.844-157_844-156ins others(17): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486338 | ||||||
| chr13:45486338
|
A | AGGGAGAG others(16): Show |
7 | a0001c0001t0001g0076a0001c0001t0001g0091a0001c0001t0001g0107others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.844-157_844-156ins others(23): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486338 | ||||||
| chr13:45486338
|
A | AGGGAGAG others(22): Show |
9 | a0001c0001t0001g0041a0001c0001t0001g0071a0001c0001t0001g0072others(6): Show | 9 | HG00438.hp1 HG01106.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-157_844-156ins others(29): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486338 | ||||||
| chr13:45486338
|
A | AGGGAGAG others(28): Show |
3 | a0001c0001t0001g0111a0001c0001t0001g0126a0001c0001t0001g0134 | 3 | HG00558.hp1 NA18964.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.844-157_844-156ins others(35): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486338 | ||||||
| chr13:45486338
|
A | AGGGAGAG others(34): Show |
2 | a0001c0001t0001g0112a0001c0001t0001g0115 | 2 | NA18939.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.844-157_844-156ins others(41): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486338 | ||||||
| chr13:45486338
|
A | G | 3 | a0002c0007t0002g0223a0002c0007t0002g0224a0002c0007t0002g0232 | 3 | HG01192.hp1 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.844-157A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486338 | ||||||
| chr13:45486338
|
AC | A | 110 | a0001c0001t0001g0059a0001c0001t0001g0062a0001c0001t0001g0063others(107): Show | 113 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.844-156delC | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486338 | ||||||
| chr13:45486339
|
C | A | 74 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0045others(71): Show | 75 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.844-156C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486339 | ||||||
| chr13:45486339
|
C | CGGAGA | 16 | a0001c0002t0001g0241a0001c0002t0001g0256a0001c0002t0001g0262others(13): Show | 16 | HG00642.hp2 HG01074.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.844-154_844-153ins others(5): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486339 | |||||
| chr13:45486339
|
C | CGGGAGA | 38 | a0001c0001t0001g0054a0001c0001t0001g0057a0002c0003t0002g0005others(35): Show | 40 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.844-131_844-126dup others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486339 | |||||
| chr13:45486339
|
C | CGGGAGAC others(5): Show |
9 | a0001c0002t0001g0253a0001c0002t0001g0254a0001c0002t0001g0255others(6): Show | 9 | HG00099.hp2 HG00733.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.844-150_844-149ins others(12): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486339 | |||||
| chr13:45486339
|
C | CGGGAGAC others(12): Show |
2 | a0001c0002t0001g0302a0001c0002t0001g0317 | 2 | HG00558.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.844-150_844-149ins others(19): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486339 | |||||
| chr13:45486339
|
C | CGGGAGAG others(5): Show |
9 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0013t0004g0194others(6): Show | 9 | HG01891.hp2 HG01943.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-137_844-126dup others(12): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486339 | |||||
| chr13:45486339
|
C | CGGGAGAG others(11): Show |
9 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0058others(6): Show | 9 | HG01123.hp1 HG02071.hp1 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.844-143_844-126dup others(18): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486339 | |||||
| chr13:45486339
|
C | CGGGAGAG others(17): Show |
9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG01167.hp2 HG01169.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-149_844-126dup others(24): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486339 | |||||
| chr13:45486339
|
C | CGGGAGAG others(23): Show |
3 | a0001c0001t0001g0044a0001c0001t0001g0096a0001c0001t0001g0130 | 3 | HG01099.hp2 HG01261.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.844-155_844-126dup others(30): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486339 | |||||
| chr13:45486339
|
C | CGGGAGAG others(29): Show |
2 | a0001c0001t0001g0090a0001c0001t0001g0239 | 2 | HG03491.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.844-126_844-125ins others(36): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486339 | |||||
| chr13:45486339
|
C | CGGGAGAG others(41): Show |
2 | a0001c0001t0001g0125a0001c0001t0001g0138 | 2 | HG02056.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.844-126_844-125ins others(48): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486339 | |||||
| chr13:45486339
|
C | G | 1 | a0002c0007t0002g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.844-156C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486339 | ||||||
| chr13:45486343
|
A | G | 34 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(31): Show | 35 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.844-152A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486343 | ||||||
| chr13:45486344
|
G | C | 1 | a0001c0001t0001g0059 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.844-151G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486344 | ||||||
| chr13:45486345
|
A | G | 1 | a0002c0007t0002g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.844-150A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486345 | ||||||
| chr13:45486349
|
A | G | 34 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(31): Show | 35 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.844-146A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486349 | ||||||
| chr13:45486355
|
A | G | 28 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(25): Show | 29 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.844-140A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486355 | ||||||
| chr13:45486361
|
A | G | 21 | a0002c0003t0002g0208a0002c0003t0002g0209a0002c0003t0002g0210others(18): Show | 21 | HG01074.hp2 HG01109.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.844-134A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486361 | ||||||
| chr13:45486950
|
A | T | 96 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(93): Show | 98 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.924+375A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45486950 | ||||||
| chr13:45486964
|
A | C | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.924+389A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45486964 | ||||||
| chr13:45486979
|
T | C | 215 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.924+404T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45486979 | ||||||
| chr13:45487021
|
A | G | 96 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(93): Show | 98 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.924+446A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45487021 | ||||||
| chr13:45487258
|
A | T | 215 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.924+683A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45487258 | ||||||
| chr13:45487412
|
T | G | 300 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(297): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.924+837T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45487412 | ||||||
| chr13:45487695
|
C | T | 3 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0231 | 3 | HG02647.hp1 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.924+1120C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45487695 | ||||||
| chr13:45487756
|
C | G | 300 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(297): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.924+1181C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45487756 | ||||||
| chr13:45487861
|
C | T | 296 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(293): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.924+1286C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45487861 | ||||||
| chr13:45487949
|
G | A | 1 | a0002c0003t0002g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.924+1374G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45487949 | ||||||
| chr13:45488024
|
A | T | 50 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(47): Show | 53 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.924+1449A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488024 | ||||||
| chr13:45488034
|
A | G | 14 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0109others(11): Show | 14 | HG00558.hp1 HG02080.hp1 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.924+1459A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488034 | ||||||
| chr13:45488155
|
G | A | 109 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037others(106): Show | 116 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.924+1580G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488155 | ||||||
| chr13:45488255
|
G | C | 8 | a0003c0006t0004g0193a0003c0006t0004g0195a0003c0006t0004g0196others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.924+1680G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488255 | ||||||
| chr13:45488306
|
AG | A | 17 | a0002c0003t0002g0208a0002c0003t0002g0209a0002c0003t0002g0210others(14): Show | 17 | HG01109.hp2 HG01361.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.924+1732delG | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488306 | ||||||
| chr13:45488334
|
C | T | 1 | a0001c0013t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.924+1759C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488334 | ||||||
| chr13:45488359
|
C | T | 1 | a0002c0003t0002g0006 | 2 | NA19002.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.924+1784C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488359 | ||||||
| chr13:45488370
|
G | T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.924+1795G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488370 | ||||||
| chr13:45488394
|
G | T | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.924+1819G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488394 | ||||||
| chr13:45488428
|
A | C | 49 | a0001c0013t0004g0194a0002c0003t0002g0005a0002c0003t0002g0006others(46): Show | 52 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.924+1853A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488428 | ||||||
| chr13:45488460
|
C | T | 25 | a0002c0004t0001g0001a0002c0004t0001g0002a0002c0004t0001g0011others(22): Show | 29 | HG00280.hp1 HG00597.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.924+1885C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488460 | ||||||
| chr13:45488734
|
G | C | 48 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(45): Show | 51 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.924+2159G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488734 | ||||||
| chr13:45488981
|
A | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0081 | 2 | HG01943.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.925-1934A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488981 | ||||||
| chr13:45488982
|
G | A | 5 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0085others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.925-1933G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488982 | ||||||
| chr13:45489009
|
G | A | 1 | a0002c0005t0001g0313 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.925-1906G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45489009 | ||||||
| chr13:45489055
|
G | C | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.925-1860G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45489055 | ||||||
| chr13:45489100
|
C | T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.925-1815C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45489100 | ||||||
| chr13:45489140
|
T | C | 2 | a0001c0002t0001g0229a0001c0002t0001g0230 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.925-1775T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45489140 | ||||||
| chr13:45489186
|
C | CAA | 6 | a0001c0001t0001g0122a0003c0006t0004g0193a0003c0006t0004g0195others(3): Show | 6 | HG01981.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.925-1704_925-1703d others(4): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489186 | |||||
| chr13:45489186
|
CA | C | 118 | a0001c0001t0001g0043a0001c0001t0001g0071a0001c0001t0001g0072others(115): Show | 120 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.925-1703delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489186 | |||||
| chr13:45489186
|
CAA | C | 6 | a0001c0001t0001g0073a0001c0002t0001g0244a0001c0002t0001g0256others(3): Show | 6 | HG01074.hp2 HG02040.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.925-1704_925-1703d others(4): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489186 | |||||
| chr13:45489186
|
CAAAAAA | C | 70 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(67): Show | 77 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.925-1708_925-1703d others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489186 | |||||
| chr13:45489186
|
CAAAAAAA | C | 9 | a0002c0003t0002g0168a0002c0005t0003g0004a0002c0005t0003g0010others(6): Show | 10 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.925-1709_925-1703d others(9): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489186 | |||||
| chr13:45489213
|
G | C | 8 | a0002c0005t0003g0004a0002c0005t0003g0010a0002c0005t0003g0155others(5): Show | 9 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.925-1702G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45489213 | ||||||
| chr13:45489223
|
G | A | 50 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0204others(47): Show | 52 | HG00099.hp2 HG00544.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.925-1692G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45489223 | ||||||
| chr13:45489262
|
C | CAAA | 33 | a0002c0004t0001g0001a0002c0004t0001g0002a0002c0004t0001g0011others(30): Show | 38 | HG00280.hp1 HG00597.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.925-1637_925-1635d others(5): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489262 | |||||
| chr13:45489262
|
C | CAAAA | 7 | a0002c0005t0003g0010a0002c0005t0003g0157a0002c0005t0003g0158others(4): Show | 7 | HG00408.hp1 HG02015.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.925-1638_925-1635d others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489262 | |||||
| chr13:45489262
|
C | CAAAAA | 36 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(33): Show | 38 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.925-1639_925-1635d others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489262 | |||||
| chr13:45489262
|
C | CAAAAAA | 20 | a0002c0003t0002g0007a0002c0003t0002g0166a0002c0003t0002g0180others(17): Show | 21 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.925-1640_925-1635d others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489262 | |||||
| chr13:45489262
|
C | CAAAAAAA | 12 | a0002c0003t0002g0202a0002c0003t0002g0208a0002c0003t0002g0209others(9): Show | 12 | HG01109.hp2 HG01192.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.925-1641_925-1635d others(9): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489262 | |||||
| chr13:45489262
|
C | CAAAAAAA others(2): Show |
11 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0072others(8): Show | 11 | HG00099.hp1 HG01167.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.925-1643_925-1635d others(11): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489262 | |||||
| chr13:45489262
|
C | CAAAAAAA others(3): Show |
132 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(129): Show | 133 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.925-1644_925-1635d others(12): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489262 | |||||
| chr13:45489262
|
C | CAAAAAAA others(4): Show |
51 | a0001c0001t0001g0047a0001c0001t0001g0055a0001c0001t0001g0067others(48): Show | 52 | HG00544.hp1 HG00642.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.925-1645_925-1635d others(13): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489262 | |||||
| chr13:45489262
|
C | CAAAAAAA others(5): Show |
19 | a0001c0002t0001g0008a0001c0002t0001g0242a0001c0002t0001g0254others(16): Show | 20 | HG00099.hp2 HG00733.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.925-1646_925-1635d others(14): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489262 | |||||
| chr13:45489262
|
C | CAAAAAAA others(6): Show |
2 | a0001c0002t0001g0298a0001c0002t0001g0321 | 2 | HG01106.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.925-1647_925-1635d others(15): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489262 | |||||
| chr13:45489362
|
A | G | 7 | a0002c0007t0002g0223a0002c0007t0002g0224a0002c0007t0002g0225others(4): Show | 7 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.925-1553A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45489362 | ||||||
| chr13:45489819
|
A | AT | 40 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(37): Show | 42 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.925-1080dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489819 | |||||
| chr13:45489819
|
AT | A | 11 | a0002c0003t0002g0208a0002c0003t0002g0209a0002c0003t0002g0211others(8): Show | 11 | HG01074.hp2 HG01109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.925-1080delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489819 | |||||
| chr13:45489819
|
ATT | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0120others(14): Show | 18 | HG01975.hp1 HG01978.hp1 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.925-1081_925-1080d others(4): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489819 | |||||
| chr13:45489819
|
ATTT | A | 208 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0043others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.925-1082_925-1080d others(5): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489819 | |||||
| chr13:45489819
|
ATTTT | A | 8 | a0002c0005t0003g0004a0002c0005t0003g0010a0002c0005t0003g0155others(5): Show | 9 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.925-1083_925-1080d others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489819 | |||||
| chr13:45489852
|
G | T | 330 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(327): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.925-1063G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45489852 | ||||||
| chr13:45489882
|
A | G | 2 | a0002c0005t0003g0010a0002c0005t0003g0192 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.925-1033A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45489882 | ||||||
| chr13:45489947
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.925-968G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45489947 | ||||||
| chr13:45490053
|
A | G | 4 | a0002c0005t0003g0151a0002c0005t0003g0152a0002c0005t0003g0153others(1): Show | 4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.925-862A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45490053 | ||||||
| chr13:45490209
|
G | A | 1 | a0001c0008t0001g0042 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.925-706G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45490209 | ||||||
| chr13:45490337
|
A | G | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.925-578A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45490337 | ||||||
| chr13:45490357
|
A | G | 2 | a0001c0002t0001g0286a0001c0002t0001g0287 | 2 | NA18951.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.925-558A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45490357 | ||||||
| chr13:45490540
|
A | T | 36 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(33): Show | 38 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.925-375A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45490540 | ||||||
| chr13:45490655
|
AAAC | A | 4 | a0002c0005t0003g0151a0002c0005t0003g0152a0002c0005t0003g0153others(1): Show | 4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.925-258_925-256del others(3): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45490655 | |||||
| chr13:45490689
|
A | G | 71 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0005others(68): Show | 74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.925-226A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45490689 | ||||||
| chr13:45490750
|
TA | T | 71 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0005others(68): Show | 74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.925-164delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45490750 | ||||||
| chr13:45491061
|
G | C | 2 | a0001c0002t0001g0146a0001c0002t0001g0147 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.968+103G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 9/22 | chr13 | 45491061 | ||||||
| chr13:45491100
|
G | A | 71 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0005others(68): Show | 74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.968+142G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 9/22 | chr13 | 45491100 | ||||||
| chr13:45491108
|
C | G | 30 | a0002c0003t0002g0202a0002c0003t0002g0208a0002c0003t0002g0209others(27): Show | 30 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.968+150C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 9/22 | chr13 | 45491108 | ||||||
| chr13:45491132
|
T | G | 3 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007 | 4 | HG01069.hp1 HG01071.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.968+174T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 9/22 | chr13 | 45491132 | ||||||
| chr13:45491169
|
A | T | 1 | a0005c0019t0001g0070 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.968+211A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 9/22 | chr13 | 45491169 | ||||||
| chr13:45491583
|
A | G | 7 | a0002c0007t0002g0223a0002c0007t0002g0224a0002c0007t0002g0225others(4): Show | 7 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1095+45A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 10/22 | chr13 | 45491583 | ||||||
| chr13:45491699
|
C | G | 1 | a0002c0004t0001g0015 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1095+161C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 10/22 | chr13 | 45491699 | ||||||
| chr13:45491878
|
TA | T | 14 | a0002c0005t0003g0004a0002c0005t0003g0010a0002c0005t0003g0151others(11): Show | 15 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1096-275delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr13 | 45491878 | |||||
| chr13:45492028
|
T | C | 218 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1096-131T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 10/22 | chr13 | 45492028 | ||||||
| chr13:45492057
|
G | A | 71 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0005others(68): Show | 74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1096-102G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 10/22 | chr13 | 45492057 | ||||||
| chr13:45492414
|
AGTTATTT others(8): Show |
A | 4 | a0002c0005t0003g0157a0002c0005t0003g0158a0002c0005t0003g0159others(1): Show | 4 | HG00408.hp1 HG02015.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1187+167_1187+181d others(17): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 45492414 | |||||
| chr13:45492438
|
TA | T | 71 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0005others(68): Show | 74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1187+190delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 45492438 | |||||
| chr13:45492464
|
G | T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1187+214G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45492464 | ||||||
| chr13:45492601
|
G | T | 1 | a0001c0002t0001g0325 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1187+351G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45492601 | ||||||
| chr13:45492691
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1187+441A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45492691 | ||||||
| chr13:45492707
|
A | G | 2 | a0001c0008t0001g0042a0001c0008t0001g0121 | 2 | HG00738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1187+457A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45492707 | ||||||
| chr13:45492719
|
A | T | 95 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(92): Show | 97 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1187+469A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45492719 | ||||||
| chr13:45492964
|
G | T | 7 | a0002c0007t0002g0223a0002c0007t0002g0224a0002c0007t0002g0225others(4): Show | 7 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1188-383G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45492964 | ||||||
| chr13:45492987
|
G | A | 1 | a0001c0013t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1188-360G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45492987 | ||||||
| chr13:45493051
|
G | A | 2 | a0002c0005t0003g0004a0002c0005t0003g0155 | 3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1188-296G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45493051 | ||||||
| chr13:45493054
|
A | G | 1 | a0002c0005t0003g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1188-293A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45493054 | ||||||
| chr13:45493067
|
T | C | 2 | a0002c0005t0011g0150a0002c0005t0012g0148 | 2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1188-280T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45493067 | ||||||
| chr13:45493147
|
G | A | 2 | a0001c0002t0001g0229a0001c0002t0001g0230 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1188-200G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45493147 | ||||||
| chr13:45493192
|
G | A | 1 | a0001c0002t0001g0247 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1188-155G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45493192 | ||||||
| chr13:45493569
|
C | CAGGGAA | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1327+83_1327+84ins others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45493569 | ||||||
| chr13:45493570
|
C | T | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1327+84C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45493570 | ||||||
| chr13:45493572
|
C | T | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1327+86C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45493572 | ||||||
| chr13:45493866
|
G | GT | 303 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(300): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.1327+384dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr13 | 45493866 | |||||
| chr13:45493875
|
A | G | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1327+389A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45493875 | ||||||
| chr13:45493909
|
A | G | 4 | a0002c0005t0003g0157a0002c0005t0003g0158a0002c0005t0003g0159others(1): Show | 4 | HG00408.hp1 HG02015.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1327+423A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45493909 | ||||||
| chr13:45493961
|
C | G | 1 | a0002c0003t0002g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1327+475C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45493961 | ||||||
| chr13:45494018
|
A | G | 4 | a0001c0002t0001g0254a0001c0002t0001g0298a0001c0002t0001g0300others(1): Show | 4 | HG00099.hp2 HG01106.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1327+532A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494018 | ||||||
| chr13:45494036
|
C | G | 1 | a0002c0004t0001g0012 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1327+550C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494036 | ||||||
| chr13:45494215
|
C | T | 2 | a0001c0002t0001g0296a0007c0017t0001g0285 | 2 | NA18973.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1327+729C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494215 | ||||||
| chr13:45494268
|
T | C | 3 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007 | 4 | HG01069.hp1 HG01071.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1327+782T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494268 | ||||||
| chr13:45494281
|
C | T | 37 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(34): Show | 39 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.1327+795C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494281 | ||||||
| chr13:45494325
|
T | TA | 17 | a0001c0001t0001g0067a0001c0001t0001g0081a0001c0001t0001g0085others(14): Show | 17 | HG00738.hp2 HG01978.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.1327+858dupA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr13 | 45494325 | |||||
| chr13:45494325
|
TA | T | 16 | a0001c0001t0001g0068a0002c0003t0002g0219a0002c0003t0002g0231others(13): Show | 17 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1327+858delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr13 | 45494325 | |||||
| chr13:45494341
|
A | C | 1 | a0002c0003t0002g0179 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1327+855A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494341 | ||||||
| chr13:45494348
|
C | A | 37 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(34): Show | 39 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.1327+862C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494348 | ||||||
| chr13:45494462
|
C | T | 1 | a0001c0002t0001g0146 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1327+976C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494462 | ||||||
| chr13:45494616
|
C | G | 4 | a0002c0005t0003g0151a0002c0005t0003g0152a0002c0005t0003g0153others(1): Show | 4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1327+1130C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494616 | ||||||
| chr13:45494765
|
G | C | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1327+1279G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494765 | ||||||
| chr13:45494864
|
C | CT | 208 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(205): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1328-1274dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr13 | 45494864 | |||||
| chr13:45494864
|
CT | C | 71 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0005others(68): Show | 74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1328-1274delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr13 | 45494864 | |||||
| chr13:45494871
|
T | C | 1 | a0001c0013t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1328-1281T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494871 | ||||||
| chr13:45494914
|
C | T | 4 | a0002c0005t0003g0157a0002c0005t0003g0158a0002c0005t0003g0159others(1): Show | 4 | HG00408.hp1 HG02015.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1328-1238C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494914 | ||||||
| chr13:45494915
|
G | A | 1 | a0002c0003t0002g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1328-1237G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494915 | ||||||
| chr13:45494980
|
G | A | 1 | a0002c0003t0002g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1328-1172G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494980 | ||||||
| chr13:45494997
|
C | T | 1 | a0001c0002t0001g0324 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1328-1155C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494997 | ||||||
| chr13:45495063
|
C | G | 71 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0005others(68): Show | 74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1328-1089C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45495063 | ||||||
| chr13:45495068
|
T | C | 36 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(33): Show | 38 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.1328-1084T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45495068 | ||||||
| chr13:45495122
|
C | G | 303 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(300): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.1328-1030C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45495122 | ||||||
| chr13:45495145
|
CT | C | 288 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(285): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.1328-986delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr13 | 45495145 | |||||
| chr13:45495145
|
CTTTTTTT others(4): Show |
C | 1 | a0002c0005t0003g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1328-996_1328-986d others(13): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr13 | 45495145 | |||||
| chr13:45495180
|
G | A | 1 | a0002c0003t0002g0215 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1328-972G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45495180 | ||||||
| chr13:45495241
|
G | A | 2 | a0002c0003t0002g0184a0002c0003t0002g0185 | 2 | NA18939.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1328-911G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45495241 | ||||||
| chr13:45495256
|
G | A | 5 | a0003c0006t0004g0195a0003c0006t0004g0196a0003c0006t0004g0197others(2): Show | 5 | HG02559.hp2 HG02717.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1328-896G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45495256 | ||||||
| chr13:45495660
|
G | A | 4 | a0002c0005t0003g0151a0002c0005t0003g0152a0002c0005t0003g0153others(1): Show | 4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1328-492G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45495660 | ||||||
| chr13:45495769
|
C | T | 303 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(300): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.1328-383C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45495769 | ||||||
| chr13:45495786
|
A | T | 8 | a0002c0005t0003g0004a0002c0005t0003g0010a0002c0005t0003g0155others(5): Show | 9 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1328-366A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45495786 | ||||||
| chr13:45496354
|
C | T | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1488+42C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496354 | ||||||
| chr13:45496374
|
T | C | 5 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1488+62T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496374 | ||||||
| chr13:45496375
|
A | AT | 4 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(1): Show | 5 | HG01069.hp1 HG01071.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1488+70dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45496375 | |||||
| chr13:45496404
|
G | A | 3 | a0001c0002t0001g0204a0001c0002t0001g0329a0001c0002t0001g0330 | 3 | HG01256.hp2 NA19064.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1488+92G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496404 | ||||||
| chr13:45496653
|
T | G | 1 | a0002c0004t0001g0030 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1488+341T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496653 | ||||||
| chr13:45496773
|
G | A | 4 | a0002c0005t0003g0157a0002c0005t0003g0158a0002c0005t0003g0159others(1): Show | 4 | HG00408.hp1 HG02015.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1488+461G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496773 | ||||||
| chr13:45496775
|
G | A | 1 | a0001c0013t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1488+463G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496775 | ||||||
| chr13:45496796
|
C | T | 2 | a0002c0003t0002g0184a0002c0003t0002g0185 | 2 | NA18939.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1488+484C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496796 | ||||||
| chr13:45496814
|
C | T | 2 | a0002c0005t0003g0004a0002c0005t0003g0155 | 3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1488+502C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496814 | ||||||
| chr13:45496915
|
C | T | 218 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1488+603C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496915 | ||||||
| chr13:45496920
|
G | A | 1 | a0001c0013t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1488+608G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496920 | ||||||
| chr13:45496920
|
G | C | 1 | a0002c0004t0001g0029 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1488+608G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496920 | ||||||
| chr13:45496921
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1488+609C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496921 | ||||||
| chr13:45497034
|
G | A | 230 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(227): Show | 234 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.1488+722G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45497034 | ||||||
| chr13:45497041
|
A | G | 1 | a0002c0003t0002g0240 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1488+729A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45497041 | ||||||
| chr13:45497079
|
T | C | 8 | a0002c0005t0003g0004a0002c0005t0003g0010a0002c0005t0003g0155others(5): Show | 9 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1488+767T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45497079 | ||||||
| chr13:45497085
|
T | C | 218 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1488+773T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45497085 | ||||||
| chr13:45497191
|
C | T | 1 | a0002c0004t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1488+879C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45497191 | ||||||
| chr13:45497192
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1488+880G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45497192 | ||||||
| chr13:45497479
|
G | A | 1 | a0001c0002t0001g0315 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1488+1167G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45497479 | ||||||
| chr13:45497591
|
C | G | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1488+1279C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45497591 | ||||||
| chr13:45497764
|
T | C | 303 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(300): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.1488+1452T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45497764 | ||||||
| chr13:45497784
|
T | TCAA | 8 | a0003c0006t0004g0193a0003c0006t0004g0195a0003c0006t0004g0196others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1488+1506_1488+150 others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45497784 | |||||
| chr13:45497784
|
T | TCAACAA | 5 | a0001c0001t0001g0043a0001c0001t0001g0074a0001c0001t0001g0081others(2): Show | 5 | HG01943.hp2 HG03225.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1488+1503_1488+150 others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45497784 | |||||
| chr13:45497784
|
T | TCAACAAC others(2): Show |
117 | a0001c0001t0001g0003a0001c0001t0001g0044a0001c0001t0001g0045others(114): Show | 119 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1488+1500_1488+150 others(13): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45497784 | |||||
| chr13:45497784
|
T | TCAACAAC others(5): Show |
119 | a0001c0001t0001g0041a0001c0001t0001g0073a0001c0001t0001g0076others(116): Show | 121 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1488+1497_1488+150 others(16): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45497784 | |||||
| chr13:45497784
|
T | TCAACAAC others(8): Show |
27 | a0001c0001t0001g0040a0001c0002t0001g0260a0001c0002t0001g0275others(24): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1488+1494_1488+150 others(19): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45497784 | |||||
| chr13:45497784
|
T | TCAACAAC others(11): Show |
9 | a0002c0003t0002g0005a0002c0003t0002g0160a0002c0003t0002g0166others(6): Show | 10 | HG02040.hp1 HG02132.hp1 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.1488+1491_1488+150 others(22): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45497784 | |||||
| chr13:45497784
|
T | TCAACAAC others(14): Show |
1 | a0002c0003t0002g0186 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1488+1488_1488+150 others(25): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45497784 | |||||
| chr13:45497784
|
T | TCAACAAC others(17): Show |
1 | a0002c0003t0002g0162 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1488+1485_1488+150 others(28): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45497784 | |||||
| chr13:45497812
|
CAACAACA | C | 10 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0005t0003g0004others(7): Show | 11 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1488+1503_1488+150 others(11): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45497812 | |||||
| chr13:45497815
|
CAACA | C | 4 | a0002c0005t0003g0151a0002c0005t0003g0152a0002c0005t0003g0153others(1): Show | 4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1488+1506_1488+150 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45497815 | |||||
| chr13:45497845
|
G | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(106): Show | 110 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1488+1533G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45497845 | ||||||
| chr13:45498191
|
A | G | 1 | a0002c0007t0002g0228 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1488+1879A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498191 | ||||||
| chr13:45498228
|
C | T | 7 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037others(4): Show | 7 | HG02257.hp2 HG02451.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1488+1916C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498228 | ||||||
| chr13:45498234
|
A | G | 218 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1488+1922A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498234 | ||||||
| chr13:45498251
|
A | C | 2 | a0002c0005t0003g0004a0002c0005t0003g0155 | 3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1488+1939A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498251 | ||||||
| chr13:45498298
|
C | T | 95 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(92): Show | 97 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1488+1986C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498298 | ||||||
| chr13:45498356
|
C | CT | 86 | a0001c0001t0001g0076a0001c0002t0001g0008a0001c0002t0001g0009others(83): Show | 88 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1488+2064dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45498356 | |||||
| chr13:45498356
|
C | CTT | 10 | a0001c0002t0001g0262a0001c0002t0001g0284a0001c0002t0001g0292others(7): Show | 10 | HG00438.hp2 HG00642.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.1488+2063_1488+206 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45498356 | |||||
| chr13:45498356
|
CT | C | 53 | a0001c0001t0001g0048a0001c0001t0001g0059a0001c0001t0001g0098others(50): Show | 56 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.1488+2064delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45498356 | |||||
| chr13:45498356
|
CTT | C | 32 | a0001c0002t0001g0230a0002c0003t0002g0007a0002c0003t0002g0167others(29): Show | 33 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1488+2063_1488+206 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45498356 | |||||
| chr13:45498356
|
CTTT | C | 7 | a0001c0002t0001g0229a0002c0003t0002g0233a0002c0003t0002g0234others(4): Show | 7 | HG01074.hp2 HG02622.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1488+2062_1488+206 others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45498356 | |||||
| chr13:45498385
|
G | GTT | 3 | a0002c0004t0001g0018a0002c0004t0001g0028a0002c0004t0001g0030 | 3 | HG00280.hp1 HG00642.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.1488+2075_1488+207 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45498385 | |||||
| chr13:45498420
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1488+2108C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498420 | ||||||
| chr13:45498431
|
C | G | 36 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(33): Show | 38 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.1488+2119C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498431 | ||||||
| chr13:45498464
|
A | C | 8 | a0002c0005t0003g0004a0002c0005t0003g0010a0002c0005t0003g0155others(5): Show | 9 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1488+2152A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498464 | ||||||
| chr13:45498711
|
G | C | 4 | a0002c0005t0003g0151a0002c0005t0003g0152a0002c0005t0003g0153others(1): Show | 4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1488+2399G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498711 | ||||||
| chr13:45498717
|
G | A | 1 | a0002c0005t0013g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1488+2405G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498717 | ||||||
| chr13:45498798
|
T | TTCC | 7 | a0002c0007t0002g0223a0002c0007t0002g0224a0002c0007t0002g0225others(4): Show | 7 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1488+2486_1488+248 others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498798 | ||||||
| chr13:45498798
|
T | TTTC | 59 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0005others(56): Show | 62 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1488+2486_1488+248 others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498798 | ||||||
| chr13:45498814
|
A | G | 24 | a0002c0003t0002g0007a0002c0003t0002g0202a0002c0003t0002g0208others(21): Show | 25 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1488+2502A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498814 | ||||||
| chr13:45499214
|
A | G | 1 | a0002c0003t0002g0170 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1488+2902A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45499214 | ||||||
| chr13:45499325
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1488+3013C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45499325 | ||||||
| chr13:45499402
|
G | A | 71 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0005others(68): Show | 74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1488+3090G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45499402 | ||||||
| chr13:45499666
|
A | G | 1 | a0002c0003t0002g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1488+3354A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45499666 | ||||||
| chr13:45499759
|
C | T | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1488+3447C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45499759 | ||||||
| chr13:45499760
|
G | A | 1 | a0002c0005t0013g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1488+3448G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45499760 | ||||||
| chr13:45499851
|
A | G | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1489-3393A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45499851 | ||||||
| chr13:45499885
|
G | C | 1 | a0001c0001t0001g0084 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1489-3359G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45499885 | ||||||
| chr13:45500017
|
TAA | T | 10 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(7): Show | 11 | HG00621.hp1 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1489-3219_1489-321 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500017 | |||||
| chr13:45500023
|
AAAATAT | A | 14 | a0002c0003t0002g0208a0002c0003t0002g0210a0002c0003t0002g0213others(11): Show | 14 | HG01074.hp2 HG01109.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1489-3219_1489-321 others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500023 | |||||
| chr13:45500025
|
A | T | 276 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(273): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.1489-3219A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500025 | ||||||
| chr13:45500027
|
T | C | 4 | a0002c0005t0003g0151a0002c0005t0003g0152a0002c0005t0003g0153others(1): Show | 4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1489-3217T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500027 | ||||||
| chr13:45500034
|
ATATGTAT others(1): Show |
A | 25 | a0002c0003t0002g0144a0002c0003t0002g0160a0002c0003t0002g0161others(22): Show | 25 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.1489-3208_1489-320 others(12): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500034 | |||||
| chr13:45500036
|
A | G | 22 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0163others(19): Show | 24 | HG00280.hp2 HG00597.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1489-3208A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500036 | ||||||
| chr13:45500038
|
G | A | 14 | a0002c0003t0002g0208a0002c0003t0002g0210a0002c0003t0002g0213others(11): Show | 14 | HG01074.hp2 HG01109.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1489-3206G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500038 | ||||||
| chr13:45500038
|
GTA | G | 4 | a0002c0003t0002g0209a0002c0003t0002g0211a0002c0003t0002g0212others(1): Show | 4 | HG02145.hp1 HG02647.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1489-3204_1489-320 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500038 | |||||
| chr13:45500040
|
A | G | 29 | a0001c0002t0001g0229a0001c0002t0001g0230a0001c0002t0001g0272others(26): Show | 32 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1489-3204A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500040 | ||||||
| chr13:45500040
|
ATGTG | A | 4 | a0002c0004t0001g0017a0002c0004t0001g0033a0002c0005t0011g0150others(1): Show | 4 | HG03139.hp1 NA18522.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1489-3181_1489-317 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500040 | |||||
| chr13:45500055
|
T | A | 1 | a0001c0002t0001g0203 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1489-3189T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500055 | ||||||
| chr13:45500057
|
T | A | 218 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1489-3187T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500057 | ||||||
| chr13:45500059
|
T | A | 11 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0163others(8): Show | 13 | HG00280.hp2 HG00597.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1489-3185T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500059 | ||||||
| chr13:45500061
|
T | A | 14 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0007others(11): Show | 15 | HG00621.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1489-3183T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500061 | ||||||
| chr13:45500061
|
TGTGTGA | T | 4 | a0002c0005t0003g0151a0002c0005t0003g0152a0002c0005t0003g0153others(1): Show | 4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1489-3177_1489-317 others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500061 | |||||
| chr13:45500063
|
T | A | 5 | a0002c0003t0002g0217a0002c0005t0003g0004a0002c0005t0003g0010others(2): Show | 6 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1489-3181T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500063 | ||||||
| chr13:45500065
|
T | A | 5 | a0002c0003t0002g0202a0002c0005t0003g0157a0002c0005t0003g0158others(2): Show | 5 | HG00408.hp1 HG02015.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489-3179T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500065 | ||||||
| chr13:45500065
|
TGA | T | 3 | a0001c0002t0001g0263a0002c0005t0003g0010a0002c0005t0003g0192 | 3 | HG02723.hp1 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1489-3177_1489-317 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500065 | |||||
| chr13:45500067
|
A | T | 252 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(249): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.1489-3177A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500067 | ||||||
| chr13:45500069
|
T | A | 5 | a0002c0004t0001g0030a0002c0005t0003g0151a0002c0005t0003g0152others(2): Show | 5 | HG01257.hp1 HG01975.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489-3175T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500069 | ||||||
| chr13:45500086
|
GTGTGTGT others(5): Show |
G | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1489-3156_1489-314 others(16): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500086 | |||||
| chr13:45500088
|
GTGTGTGT others(11): Show |
G | 1 | a0001c0001t0001g0138 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1489-3154_1489-313 others(22): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500088 | |||||
| chr13:45500088
|
GTGTGTGT others(13): Show |
G | 1 | a0001c0001t0001g0124 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1489-3154_1489-313 others(24): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500088 | |||||
| chr13:45500090
|
GTGTGTAT others(11): Show |
G | 2 | a0001c0001t0001g0137a0002c0012t0001g0103 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1489-3152_1489-313 others(22): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500090 | |||||
| chr13:45500092
|
G | A | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1489-3152G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500092 | ||||||
| chr13:45500092
|
GTGTATAT others(9): Show |
G | 81 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0043others(78): Show | 82 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1489-3150_1489-313 others(20): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500092 | |||||
| chr13:45500092
|
GTGTATAT others(11): Show |
G | 1 | a0001c0002t0001g0203 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1489-3150_1489-313 others(22): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500092 | |||||
| chr13:45500094
|
G | A | 5 | a0002c0005t0003g0151a0002c0005t0003g0152a0002c0005t0003g0153others(2): Show | 5 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489-3150G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500094 | ||||||
| chr13:45500094
|
G | GTGTGTGT others(3): Show |
2 | a0002c0005t0003g0004a0002c0005t0003g0155 | 3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1489-3149_1489-314 others(14): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500094 | |||||
| chr13:45500094
|
GTA | G | 26 | a0002c0003t0002g0240a0002c0004t0001g0001a0002c0004t0001g0002others(23): Show | 30 | HG00280.hp1 HG00597.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1489-3129_1489-312 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500094 | |||||
| chr13:45500094
|
GTATA | G | 3 | a0002c0003t0002g0236a0002c0003t0002g0238a0002c0005t0012g0148 | 3 | HG03139.hp1 HG03654.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1489-3131_1489-312 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500094 | |||||
| chr13:45500094
|
GTATATA | G | 15 | a0001c0001t0001g0082a0001c0002t0001g0205a0001c0002t0001g0288others(12): Show | 17 | HG00408.hp1 HG00597.hp2 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.1489-3133_1489-312 others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500094 | |||||
| chr13:45500094
|
GTATATAT others(1): Show |
G | 28 | a0001c0002t0001g0244a0001c0002t0001g0254a0001c0002t0001g0264others(25): Show | 28 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1489-3135_1489-312 others(12): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500094 | |||||
| chr13:45500094
|
GTATATAT others(3): Show |
G | 53 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0035others(50): Show | 55 | HG00280.hp2 HG00544.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1489-3137_1489-312 others(14): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500094 | |||||
| chr13:45500094
|
GTATATAT others(5): Show |
G | 24 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(21): Show | 24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.1489-3139_1489-312 others(16): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500094 | |||||
| chr13:45500094
|
GTATATAT others(7): Show |
G | 17 | a0001c0001t0001g0040a0001c0001t0001g0047a0001c0001t0001g0054others(14): Show | 17 | HG00408.hp2 HG00733.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.1489-3141_1489-312 others(18): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500094 | |||||
| chr13:45500094
|
GTATATAT others(9): Show |
G | 18 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0002t0001g0253others(15): Show | 18 | HG01106.hp1 HG02040.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1489-3143_1489-312 others(20): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500094 | |||||
| chr13:45500096
|
A | G | 48 | a0001c0002t0001g0263a0002c0003t0002g0144a0002c0003t0002g0160others(45): Show | 48 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.1489-3148A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500096 | ||||||
| chr13:45500098
|
A | G | 49 | a0001c0002t0001g0263a0002c0003t0002g0144a0002c0003t0002g0160others(46): Show | 49 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1489-3146A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500098 | ||||||
| chr13:45500100
|
A | G | 50 | a0001c0002t0001g0263a0002c0003t0002g0144a0002c0003t0002g0160others(47): Show | 50 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1489-3144A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500100 | ||||||
| chr13:45500102
|
A | G | 59 | a0001c0001t0001g0082a0001c0002t0001g0205a0001c0002t0001g0263others(56): Show | 61 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.1489-3142A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500102 | ||||||
| chr13:45500104
|
A | G | 67 | a0001c0001t0001g0082a0001c0002t0001g0205a0001c0002t0001g0244others(64): Show | 69 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.1489-3140A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500104 | ||||||
| chr13:45500106
|
A | G | 76 | a0001c0001t0001g0082a0001c0002t0001g0008a0001c0002t0001g0009others(73): Show | 78 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1489-3138A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500106 | ||||||
| chr13:45500108
|
A | G | 97 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(94): Show | 99 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1489-3136A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500108 | ||||||
| chr13:45500110
|
A | G | 84 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0035others(81): Show | 86 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1489-3134A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500110 | ||||||
| chr13:45500112
|
A | G | 3 | a0001c0002t0001g0286a0001c0002t0001g0287a0001c0002t0001g0324 | 3 | NA18951.hp1 NA18962.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1489-3132A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500112 | ||||||
| chr13:45500117
|
A | T | 2 | a0002c0005t0013g0154a0002c0005t0014g0206 | 2 | HG01975.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1489-3127A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500117 | ||||||
| chr13:45500306
|
A | G | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1489-2938A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500306 | ||||||
| chr13:45500697
|
G | A | 16 | a0001c0002t0001g0253a0001c0002t0001g0255a0001c0002t0001g0256others(13): Show | 16 | HG02040.hp2 HG02071.hp2 NA18943.hp2 others(13): Show |
intron_variant | MODIFIER | c.1489-2547G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500697 | ||||||
| chr13:45500822
|
G | C | 1 | a0001c0002t0001g0281 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1489-2422G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500822 | ||||||
| chr13:45500864
|
C | T | 14 | a0002c0005t0003g0004a0002c0005t0003g0010a0002c0005t0003g0151others(11): Show | 15 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1489-2380C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500864 | ||||||
| chr13:45500933
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1489-2311C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500933 | ||||||
| chr13:45501158
|
A | G | 111 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(108): Show | 112 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1489-2086A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45501158 | ||||||
| chr13:45501245
|
G | A | 289 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1489-1999G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45501245 | ||||||
| chr13:45501252
|
C | T | 1 | a0002c0005t0013g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1489-1992C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45501252 | ||||||
| chr13:45501289
|
C | G | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1489-1955C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45501289 | ||||||
| chr13:45501292
|
G | A | 289 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1489-1952G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45501292 | ||||||
| chr13:45501389
|
G | A | 36 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(33): Show | 38 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.1489-1855G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45501389 | ||||||
| chr13:45501390
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0065 | 2 | HG02523.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1489-1854G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45501390 | ||||||
| chr13:45501493
|
A | G | 71 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0005others(68): Show | 74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1489-1751A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45501493 | ||||||
| chr13:45501529
|
T | C | 303 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(300): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.1489-1715T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45501529 | ||||||
| chr13:45501603
|
C | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(106): Show | 110 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1489-1641C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45501603 | ||||||
| chr13:45502467
|
A | T | 303 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(300): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.1489-777A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45502467 | ||||||
| chr13:45502523
|
G | C | 1 | a0001c0001t0001g0124 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1489-721G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45502523 | ||||||
| chr13:45502960
|
C | A | 2 | a0002c0003t0002g0166a0002c0003t0002g0173 | 2 | NA18612.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.1489-284C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45502960 | ||||||
| chr13:45503165
|
T | C | 1 | a0002c0004t0001g0026 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1489-79T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45503165 | ||||||
| chr13:45503166
|
G | A | 289 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1489-78G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45503166 | ||||||
| chr13:45503621
|
G | A | 2 | a0002c0005t0003g0004a0002c0005t0003g0155 | 3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1594+272G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45503621 | ||||||
| chr13:45503958
|
A | G | 2 | a0004c0009t0001g0021a0004c0009t0001g0022 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1594+609A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45503958 | ||||||
| chr13:45503986
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1594+637T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45503986 | ||||||
| chr13:45504106
|
G | A | 1 | a0002c0004t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1594+757G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504106 | ||||||
| chr13:45504124
|
A | G | 7 | a0002c0007t0002g0223a0002c0007t0002g0224a0002c0007t0002g0225others(4): Show | 7 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1594+775A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504124 | ||||||
| chr13:45504175
|
C | T | 1 | a0001c0002t0001g0320 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1594+826C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504175 | ||||||
| chr13:45504252
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1594+903T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504252 | ||||||
| chr13:45504285
|
G | C | 218 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1594+936G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504285 | ||||||
| chr13:45504357
|
C | A | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1594+1008C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504357 | ||||||
| chr13:45504408
|
C | T | 2 | a0002c0005t0003g0004a0002c0005t0003g0155 | 3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1594+1059C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504408 | ||||||
| chr13:45504419
|
C | T | 4 | a0001c0002t0001g0009a0001c0002t0001g0276a0001c0002t0001g0314others(1): Show | 5 | HG01978.hp1 NA18971.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.1594+1070C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504419 | ||||||
| chr13:45504565
|
T | C | 21 | a0002c0003t0002g0208a0002c0003t0002g0209a0002c0003t0002g0210others(18): Show | 21 | HG01074.hp2 HG01109.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.1594+1216T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504565 | ||||||
| chr13:45504642
|
G | T | 7 | a0002c0007t0002g0223a0002c0007t0002g0224a0002c0007t0002g0225others(4): Show | 7 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1594+1293G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504642 | ||||||
| chr13:45504788
|
G | A | 1 | a0002c0004t0001g0028 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1594+1439G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504788 | ||||||
| chr13:45504861
|
C | T | 1 | a0002c0003t0002g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1594+1512C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504861 | ||||||
| chr13:45505167
|
A | G | 2 | a0002c0005t0003g0158a0002c0005t0003g0159 | 2 | HG00408.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1594+1818A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505167 | ||||||
| chr13:45505206
|
G | A | 2 | a0001c0002t0001g0229a0001c0002t0001g0230 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1594+1857G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505206 | ||||||
| chr13:45505305
|
C | CT | 218 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1594+1968dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45505305 | |||||
| chr13:45505309
|
T | G | 1 | a0002c0003t0002g0240 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1594+1960T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505309 | ||||||
| chr13:45505394
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0118 | 2 | NA18966.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1594+2045C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505394 | ||||||
| chr13:45505403
|
G | A | 2 | a0002c0003t0002g0189a0002c0003t0002g0190 | 2 | HG00597.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1594+2054G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505403 | ||||||
| chr13:45505459
|
G | A | 71 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0005others(68): Show | 74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1594+2110G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505459 | ||||||
| chr13:45505493
|
G | A | 1 | a0002c0004t0001g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1594+2144G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505493 | ||||||
| chr13:45505589
|
G | GCCACTGC others(7): Show |
2 | a0002c0005t0003g0004a0002c0005t0003g0155 | 3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1594+2242_1594+225 others(18): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45505589 | |||||
| chr13:45505601
|
G | A | 68 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(65): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1594+2252G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505601 | ||||||
| chr13:45505656
|
G | A | 1 | a0002c0003t0002g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1594+2307G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505656 | ||||||
| chr13:45505689
|
G | A | 4 | a0002c0005t0003g0151a0002c0005t0003g0152a0002c0005t0003g0153others(1): Show | 4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1594+2340G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505689 | ||||||
| chr13:45505784
|
G | A | 1 | a0002c0003t0002g0007 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1594+2435G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505784 | ||||||
| chr13:45505790
|
C | T | 3 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0005t0014g0206 | 3 | HG02922.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1594+2441C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505790 | ||||||
| chr13:45505800
|
C | T | 2 | a0001c0002t0001g0229a0001c0002t0001g0230 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1594+2451C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505800 | ||||||
| chr13:45505942
|
A | T | 1 | a0001c0001t0001g0123 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1594+2593A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505942 | ||||||
| chr13:45506014
|
A | G | 71 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0005others(68): Show | 74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1594+2665A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506014 | ||||||
| chr13:45506072
|
CT | C | 289 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1594+2729delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45506072 | |||||
| chr13:45506152
|
G | A | 218 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1594+2803G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506152 | ||||||
| chr13:45506285
|
C | T | 1 | a0002c0005t0003g0157 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1594+2936C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506285 | ||||||
| chr13:45506314
|
A | G | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1594+2965A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506314 | ||||||
| chr13:45506317
|
C | G | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1594+2968C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506317 | ||||||
| chr13:45506370
|
G | A | 68 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(65): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1594+3021G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506370 | ||||||
| chr13:45506374
|
T | C | 68 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(65): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1594+3025T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506374 | ||||||
| chr13:45506489
|
A | T | 1 | a0002c0004t0001g0016 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1594+3140A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506489 | ||||||
| chr13:45506497
|
C | T | 286 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(283): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.1594+3148C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506497 | ||||||
| chr13:45506510
|
G | A | 1 | a0002c0003t0002g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1594+3161G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506510 | ||||||
| chr13:45506540
|
C | T | 1 | a0002c0003t0002g0216 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1595-3152C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506540 | ||||||
| chr13:45506544
|
T | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0116 | 2 | HG00438.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1595-3148T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506544 | ||||||
| chr13:45506549
|
G | A | 289 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1595-3143G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506549 | ||||||
| chr13:45506728
|
A | G | 36 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(33): Show | 38 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.1595-2964A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506728 | ||||||
| chr13:45506763
|
C | T | 2 | a0002c0005t0003g0010a0002c0005t0003g0192 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1595-2929C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506763 | ||||||
| chr13:45506931
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1595-2761G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506931 | ||||||
| chr13:45506959
|
G | T | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1595-2733G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506959 | ||||||
| chr13:45506973
|
C | T | 4 | a0002c0005t0003g0151a0002c0005t0003g0152a0002c0005t0003g0153others(1): Show | 4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1595-2719C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506973 | ||||||
| chr13:45507081
|
G | T | 303 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(300): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.1595-2611G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507081 | ||||||
| chr13:45507091
|
C | T | 4 | a0002c0005t0003g0151a0002c0005t0003g0152a0002c0005t0003g0153others(1): Show | 4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1595-2601C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507091 | ||||||
| chr13:45507092
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1595-2600G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507092 | ||||||
| chr13:45507237
|
C | T | 1 | a0002c0003t0002g0240 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1595-2455C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507237 | ||||||
| chr13:45507272
|
A | G | 218 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1595-2420A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507272 | ||||||
| chr13:45507402
|
T | TGA | 3 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0005t0014g0206 | 3 | HG02922.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1595-2279_1595-227 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45507402 | |||||
| chr13:45507493
|
G | A | 1 | a0002c0005t0003g0158 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1595-2199G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507493 | ||||||
| chr13:45507497
|
G | A | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1595-2195G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507497 | ||||||
| chr13:45507644
|
A | C | 31 | a0002c0003t0002g0007a0002c0003t0002g0202a0002c0003t0002g0208others(28): Show | 32 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1595-2048A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507644 | ||||||
| chr13:45507658
|
G | A | 1 | a0002c0004t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1595-2034G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507658 | ||||||
| chr13:45507756
|
C | G | 3 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0005t0014g0206 | 3 | HG02922.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1595-1936C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507756 | ||||||
| chr13:45507774
|
G | GA | 66 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(63): Show | 68 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.1595-1905dupA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45507774 | |||||
| chr13:45507774
|
GA | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.1595-1905delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45507774 | |||||
| chr13:45507799
|
G | A | 3 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0005t0014g0206 | 3 | HG02922.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1595-1893G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507799 | ||||||
| chr13:45507954
|
A | T | 1 | a0002c0003t0002g0006 | 2 | NA19002.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1595-1738A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507954 | ||||||
| chr13:45507994
|
A | G | 4 | a0002c0005t0003g0151a0002c0005t0003g0152a0002c0005t0003g0153others(1): Show | 4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1595-1698A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507994 | ||||||
| chr13:45508023
|
T | C | 295 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(292): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.1595-1669T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508023 | ||||||
| chr13:45508028
|
C | T | 1 | a0002c0004t0001g0002 | 3 | NA18964.hp1 NA18969.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1595-1664C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508028 | ||||||
| chr13:45508033
|
C | T | 2 | a0001c0002t0001g0146a0001c0002t0001g0147 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1595-1659C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508033 | ||||||
| chr13:45508068
|
T | TA | 20 | a0001c0001t0001g0080a0001c0001t0001g0106a0001c0001t0001g0118others(17): Show | 21 | HG00642.hp1 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1595-1593dupA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | |||||
| chr13:45508068
|
T | TAA | 50 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0045others(47): Show | 53 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1595-1594_1595-159 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | |||||
| chr13:45508068
|
T | TAAA | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044others(29): Show | 32 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.1595-1595_1595-159 others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | |||||
| chr13:45508068
|
T | TAAAA | 8 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0117others(5): Show | 8 | HG00738.hp2 HG02165.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1595-1596_1595-159 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | |||||
| chr13:45508068
|
T | TAAAAA | 9 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0094others(6): Show | 9 | HG01106.hp1 HG01167.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1595-1597_1595-159 others(9): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | |||||
| chr13:45508068
|
T | TAAAAAA | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0099others(6): Show | 10 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1595-1598_1595-159 others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | |||||
| chr13:45508068
|
T | TAAAAAAA others(6): Show |
1 | a0001c0013t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1595-1605_1595-159 others(17): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | |||||
| chr13:45508068
|
T | TAAAAAAA others(11): Show |
1 | a0003c0006t0004g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1595-1610_1595-159 others(22): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | |||||
| chr13:45508068
|
T | TAAAAAAA others(12): Show |
3 | a0003c0006t0004g0193a0003c0006t0004g0199a0003c0006t0015g0200 | 3 | HG02559.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1595-1611_1595-159 others(23): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | |||||
| chr13:45508068
|
T | TAAAAAAA others(13): Show |
2 | a0003c0006t0004g0195a0003c0006t0004g0196 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1595-1612_1595-159 others(24): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | |||||
| chr13:45508068
|
T | TAAAAAAA others(14): Show |
1 | a0003c0006t0004g0197 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1595-1613_1595-159 others(25): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | |||||
| chr13:45508068
|
T | TAAAAAAA others(37): Show |
1 | a0001c0002t0001g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1595-1593_1595-159 others(48): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | |||||
| chr13:45508068
|
TA | T | 87 | a0001c0001t0001g0114a0001c0002t0001g0008a0001c0002t0001g0037others(84): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1595-1593delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | |||||
| chr13:45508068
|
TAA | T | 18 | a0001c0002t0001g0241a0002c0003t0002g0166a0002c0003t0002g0173others(15): Show | 18 | HG01074.hp1 HG01109.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.1595-1594_1595-159 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | |||||
| chr13:45508068
|
TAAAAAAA others(3): Show |
T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1595-1602_1595-159 others(14): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | |||||
| chr13:45508068
|
TAAAAAAA others(5): Show |
T | 1 | a0001c0002t0001g0283 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1595-1604_1595-159 others(16): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | |||||
| chr13:45508068
|
TAAAAAAA others(6): Show |
T | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1595-1605_1595-159 others(17): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | |||||
| chr13:45508281
|
G | C | 6 | a0002c0003t0002g0233a0002c0003t0002g0234a0002c0003t0002g0235others(3): Show | 6 | HG01074.hp2 HG02622.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1595-1411G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508281 | ||||||
| chr13:45508333
|
C | G | 9 | a0001c0013t0004g0194a0003c0006t0004g0193a0003c0006t0004g0195others(6): Show | 9 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1595-1359C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508333 | ||||||
| chr13:45508382
|
ATT | A | 93 | a0001c0001t0001g0114a0001c0002t0001g0008a0001c0002t0001g0009others(90): Show | 95 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1595-1306_1595-130 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508382 | |||||
| chr13:45508384
|
T | TTA | 83 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(80): Show | 84 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1595-1307_1595-130 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508384 | |||||
| chr13:45508384
|
T | TTATA | 4 | a0001c0001t0001g0084a0001c0001t0001g0087a0001c0008t0001g0042others(1): Show | 4 | HG00738.hp2 HG03239.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595-1307_1595-130 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508384 | |||||
| chr13:45508384
|
TTTTA | T | 44 | a0001c0002t0001g0265a0001c0002t0001g0308a0002c0003t0002g0005others(41): Show | 46 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.1595-1306_1595-130 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508384 | |||||
| chr13:45508386
|
T | A | 117 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(114): Show | 118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1595-1306T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508386 | ||||||
| chr13:45508399
|
TATATACA others(5): Show |
T | 31 | a0002c0003t0002g0007a0002c0003t0002g0202a0002c0003t0002g0208others(28): Show | 32 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1595-1291_1595-128 others(16): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508399 | |||||
| chr13:45508401
|
T | TACACAC | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1595-1290_1595-128 others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508401 | |||||
| chr13:45508403
|
T | C | 4 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1595-1289T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508403 | ||||||
| chr13:45508403
|
T | TAC | 4 | a0001c0001t0001g0056a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG00741.hp2 HG01099.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1595-1267_1595-126 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508403 | |||||
| chr13:45508403
|
T | TATATACA others(3): Show |
1 | a0001c0001t0001g0104 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1595-1288_1595-128 others(14): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508403 | |||||
| chr13:45508403
|
TAC | T | 3 | a0002c0004t0001g0012a0002c0004t0010g0025a0002c0005t0011g0150 | 3 | HG00597.hp1 HG02015.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1595-1267_1595-126 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508403 | |||||
| chr13:45508405
|
C | T | 29 | a0001c0001t0001g0045a0001c0001t0001g0057a0001c0001t0001g0069others(26): Show | 29 | HG00408.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.1595-1287C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508405 | ||||||
| chr13:45508407
|
C | T | 7 | a0002c0005t0003g0010a0002c0005t0003g0151a0002c0005t0003g0152others(4): Show | 7 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1595-1285C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508407 | ||||||
| chr13:45508409
|
C | T | 2 | a0002c0005t0003g0010a0002c0005t0003g0153 | 2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1595-1283C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508409 | ||||||
| chr13:45508419
|
C | CACACATA others(61): Show |
1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1595-1268_1595-126 others(72): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508419 | |||||
| chr13:45508419
|
CACACACA others(1): Show |
C | 36 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0160others(33): Show | 39 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1595-1267_1595-126 others(12): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508419 | |||||
| chr13:45508421
|
CACACAT | C | 6 | a0001c0013t0004g0194a0002c0003t0002g0144a0002c0003t0002g0207others(3): Show | 6 | HG00323.hp2 HG01109.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1595-1263_1595-125 others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508421 | |||||
| chr13:45508423
|
CACAT | C | 15 | a0001c0002t0001g0310a0002c0005t0003g0153a0002c0005t0003g0157others(12): Show | 15 | HG00408.hp1 HG01175.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595-1265_1595-126 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508423 | |||||
| chr13:45508425
|
CAT | C | 95 | a0001c0001t0001g0114a0001c0002t0001g0008a0001c0002t0001g0009others(92): Show | 97 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1595-1265_1595-126 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508425 | |||||
| chr13:45508427
|
T | C | 148 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 150 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1595-1265T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508427 | ||||||
| chr13:45508429
|
C | T | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1595-1263C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508429 | ||||||
| chr13:45508431
|
C | T | 2 | a0001c0002t0001g0205a0002c0005t0012g0148 | 2 | HG03139.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.1595-1261C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508431 | ||||||
| chr13:45508433
|
T | C | 5 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1595-1259T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508433 | ||||||
| chr13:45508439
|
T | C | 3 | a0002c0005t0003g0151a0002c0005t0003g0152a0002c0005t0003g0153 | 3 | HG02572.hp1 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1595-1253T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508439 | ||||||
| chr13:45508500
|
T | C | 69 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(66): Show | 72 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.1595-1192T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508500 | ||||||
| chr13:45508760
|
T | A | 1 | a0001c0001t0001g0075 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1595-932T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508760 | ||||||
| chr13:45508822
|
A | T | 211 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(208): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1595-870A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508822 | ||||||
| chr13:45509042
|
C | CT | 18 | a0001c0001t0001g0094a0001c0001t0001g0110a0001c0002t0001g0253others(15): Show | 18 | HG02040.hp2 HG02071.hp2 NA18943.hp1 others(15): Show |
intron_variant | MODIFIER | c.1595-635dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45509042 | |||||
| chr13:45509042
|
CT | C | 63 | a0001c0001t0001g0071a0002c0003t0002g0005a0002c0003t0002g0006others(60): Show | 66 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1595-635delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45509042 | |||||
| chr13:45509042
|
CTTT | C | 6 | a0002c0003t0002g0144a0002c0003t0002g0168a0002c0003t0002g0172others(3): Show | 6 | HG00280.hp2 HG00323.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.1595-637_1595-635d others(5): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45509042 | |||||
| chr13:45509337
|
C | T | 1 | a0002c0003t0002g0183 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1595-355C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45509337 | ||||||
| chr13:45509412
|
C | T | 1 | a0002c0003t0002g0006 | 2 | NA19002.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1595-280C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45509412 | ||||||
| chr13:45509495
|
G | C | 289 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1595-197G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45509495 | ||||||
| chr13:45509837
|
A | T | 1 | a0001c0002t0001g0294 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1719+21A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45509837 | ||||||
| chr13:45509990
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | NA18986.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1719+174G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45509990 | ||||||
| chr13:45510148
|
AGATG | A | 68 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(65): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1719+333_1719+336d others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45510148 | ||||||
| chr13:45510419
|
G | A | 2 | a0002c0005t0003g0010a0002c0005t0003g0192 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1719+603G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45510419 | ||||||
| chr13:45510601
|
A | G | 68 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(65): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1719+785A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45510601 | ||||||
| chr13:45510972
|
G | A | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | NA18984.hp2 NA18999.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1720-793G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45510972 | ||||||
| chr13:45511045
|
T | G | 303 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(300): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.1720-720T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45511045 | ||||||
| chr13:45511158
|
G | GT | 23 | a0002c0003t0002g0208a0002c0003t0002g0209a0002c0003t0002g0210others(20): Show | 23 | HG00408.hp1 HG01074.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1720-593dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr13 | 45511158 | |||||
| chr13:45511158
|
GT | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.1720-593delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr13 | 45511158 | |||||
| chr13:45511234
|
A | G | 36 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(33): Show | 38 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.1720-531A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45511234 | ||||||
| chr13:45511266
|
G | T | 1 | a0002c0003t0002g0181 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1720-499G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45511266 | ||||||
| chr13:45511305
|
G | A | 2 | a0002c0005t0003g0004a0002c0005t0003g0155 | 3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1720-460G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45511305 | ||||||
| chr13:45511458
|
G | A | 7 | a0002c0007t0002g0223a0002c0007t0002g0224a0002c0007t0002g0225others(4): Show | 7 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1720-307G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45511458 | ||||||
| chr13:45511564
|
G | A | 303 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(300): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.1720-201G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45511564 | ||||||
| chr13:45511611
|
T | C | 68 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(65): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1720-154T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45511611 | ||||||
| chr13:45511729
|
A | G | 289 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1720-36A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45511729 | ||||||
| chr13:45511879
|
C | G | 1 | a0002c0003t0002g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1809+25C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45511879 | ||||||
| chr13:45511920
|
A | G | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1809+66A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45511920 | ||||||
| chr13:45512004
|
T | C | 1 | a0002c0003t0002g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1809+150T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512004 | ||||||
| chr13:45512050
|
A | T | 1 | a0002c0007t0002g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1809+196A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512050 | ||||||
| chr13:45512064
|
C | T | 6 | a0002c0004t0001g0014a0002c0004t0001g0015a0002c0004t0001g0019others(3): Show | 6 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.1809+210C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512064 | ||||||
| chr13:45512108
|
CTTG | C | 4 | a0001c0001t0001g0113a0001c0001t0001g0124a0001c0001t0001g0131others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1809+259_1809+261d others(5): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45512108 | |||||
| chr13:45512146
|
T | A | 220 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1809+292T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512146 | ||||||
| chr13:45512171
|
T | C | 220 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1809+317T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512171 | ||||||
| chr13:45512330
|
C | A | 1 | a0001c0008t0001g0121 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1809+476C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512330 | ||||||
| chr13:45512452
|
C | A | 1 | a0001c0001t0001g0085 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1809+598C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512452 | ||||||
| chr13:45512494
|
T | G | 289 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1809+640T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512494 | ||||||
| chr13:45512628
|
T | C | 219 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.1809+774T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512628 | ||||||
| chr13:45512785
|
T | G | 12 | a0002c0005t0003g0004a0002c0005t0003g0010a0002c0005t0003g0151others(9): Show | 13 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1809+931T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512785 | ||||||
| chr13:45512848
|
C | T | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1809+994C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512848 | ||||||
| chr13:45512913
|
C | T | 1 | a0002c0007t0002g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1809+1059C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512913 | ||||||
| chr13:45512988
|
A | AT | 285 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(282): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.1809+1146dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45512988 | |||||
| chr13:45513006
|
G | C | 1 | a0001c0002t0001g0326 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1809+1152G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513006 | ||||||
| chr13:45513183
|
TTA | T | 21 | a0002c0003t0002g0208a0002c0003t0002g0209a0002c0003t0002g0210others(18): Show | 21 | HG01074.hp2 HG01109.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.1809+1344_1809+134 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513183 | |||||
| chr13:45513185
|
A | ATATATAT others(23): Show |
1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1809+1344_1809+137 others(34): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513185 | |||||
| chr13:45513215
|
TTA | T | 14 | a0001c0002t0001g0229a0001c0002t0001g0230a0001c0002t0001g0257others(11): Show | 14 | HG00280.hp1 HG00642.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1809+1372_1809+137 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513215 | |||||
| chr13:45513217
|
A | ATACATAT others(17): Show |
204 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(201): Show | 207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1809+1365_1809+136 others(28): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513217 | |||||
| chr13:45513217
|
A | ATACATAT others(43): Show |
3 | a0001c0002t0001g0146a0001c0002t0001g0147a0001c0002t0001g0244 | 3 | HG02451.hp2 HG02970.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1809+1365_1809+136 others(54): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513217 | |||||
| chr13:45513217
|
A | ATATATAT others(23): Show |
1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1809+1373_1809+137 others(34): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513217 | |||||
| chr13:45513217
|
ATATATAT others(45): Show |
A | 2 | a0002c0005t0003g0158a0002c0005t0003g0159 | 2 | HG00408.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1809+1372_1809+142 others(56): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513217 | |||||
| chr13:45513220
|
T | C | 4 | a0002c0005t0003g0010a0002c0005t0003g0157a0002c0005t0003g0192others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1809+1366T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513220 | ||||||
| chr13:45513222
|
T | C | 210 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(207): Show | 213 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.1809+1368T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513222 | ||||||
| chr13:45513222
|
T | TATAATAT others(17): Show |
1 | a0001c0013t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1809+1371_1809+137 others(28): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513222 | |||||
| chr13:45513222
|
TATATAAT others(145): Show |
T | 64 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(61): Show | 67 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1809+1424_1809+157 others(4): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513222 | |||||
| chr13:45513224
|
TATAATAT others(143): Show |
T | 3 | a0002c0003t0002g0217a0002c0003t0002g0219a0002c0003t0002g0240 | 3 | HG01934.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1809+1374_1809+152 others(4): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513224 | |||||
| chr13:45513248
|
CATATAAT others(17): Show |
C | 3 | a0002c0005t0003g0157a0002c0007t0002g0224a0002c0016t0003g0156 | 3 | HG01192.hp1 HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1809+1420_1809+144 others(28): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513248 | |||||
| chr13:45513250
|
T | G | 4 | a0002c0005t0003g0151a0002c0005t0003g0152a0002c0005t0003g0153others(1): Show | 4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1809+1396T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513250 | ||||||
| chr13:45513272
|
T | C | 2 | a0002c0005t0003g0158a0002c0005t0003g0159 | 2 | HG00408.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1809+1418T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513272 | ||||||
| chr13:45513272
|
T | TAC | 13 | a0001c0002t0001g0229a0001c0002t0001g0230a0001c0002t0001g0257others(10): Show | 13 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1809+1419_1809+142 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513272 | |||||
| chr13:45513274
|
T | C | 2 | a0002c0005t0011g0150a0002c0005t0012g0148 | 2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1809+1420T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513274 | ||||||
| chr13:45513295
|
A | ATATATAA others(15): Show |
1 | a0002c0005t0003g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1809+1443_1809+144 others(26): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513295 | |||||
| chr13:45513296
|
TAC | T | 3 | a0001c0002t0001g0257a0001c0014t0001g0261a0002c0005t0003g0192 | 3 | HG02723.hp1 HG04204.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.1809+1444_1809+144 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513296 | |||||
| chr13:45513298
|
C | CATATAAT others(15): Show |
1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1809+1448_1809+146 others(26): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513298 | |||||
| chr13:45513298
|
C | T | 2 | a0002c0005t0003g0010a0002c0005t0014g0206 | 2 | HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1809+1444C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513298 | ||||||
| chr13:45513298
|
CAT | C | 2 | a0002c0005t0003g0004a0002c0005t0003g0155 | 3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1809+1448_1809+144 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513298 | |||||
| chr13:45513324
|
C | T | 2 | a0002c0005t0003g0010a0002c0005t0014g0206 | 2 | HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1809+1470C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513324 | ||||||
| chr13:45513345
|
T | TTATATAT others(19): Show |
1 | a0002c0005t0003g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1809+1494_1809+151 others(30): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513345 | |||||
| chr13:45513348
|
T | TAC | 10 | a0001c0002t0001g0257a0001c0014t0001g0261a0003c0006t0004g0193others(7): Show | 10 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1809+1495_1809+149 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513348 | |||||
| chr13:45513348
|
T | TACATATA others(95): Show |
2 | a0001c0002t0001g0229a0001c0002t0001g0230 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1809+1495_1809+149 others(106): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513348 | |||||
| chr13:45513348
|
TATATAAT others(19): Show |
T | 9 | a0002c0004t0001g0002a0002c0004t0001g0011a0002c0004t0001g0012others(6): Show | 11 | HG00280.hp1 HG00597.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1809+1546_1809+157 others(30): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513348 | |||||
| chr13:45513374
|
C | CATATAAT others(17): Show |
2 | a0001c0002t0001g0146a0001c0002t0001g0147 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1809+1522_1809+154 others(28): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513374 | |||||
| chr13:45513374
|
C | CATATAAT others(45): Show |
8 | a0002c0004t0001g0001a0002c0004t0001g0016a0002c0004t0001g0017others(5): Show | 10 | HG02074.hp1 HG02165.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.1809+1545_1809+154 others(56): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513374 | |||||
| chr13:45513374
|
C | T | 2 | a0002c0005t0003g0010a0002c0005t0003g0192 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1809+1520C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513374 | ||||||
| chr13:45513395
|
TTATACAT others(21): Show |
T | 3 | a0002c0005t0003g0151a0002c0005t0003g0152a0002c0005t0003g0153 | 3 | HG02572.hp1 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1809+1546_1809+157 others(32): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513395 | |||||
| chr13:45513395
|
TTATACAT others(47): Show |
T | 1 | a0002c0005t0013g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1809+1546_1809+159 others(58): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513395 | |||||
| chr13:45513395
|
TTATACAT others(99): Show |
T | 1 | a0002c0007t0002g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1809+1546_1809+165 others(4): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513395 | |||||
| chr13:45513398
|
TAC | T | 115 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(112): Show | 116 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1809+1546_1809+154 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513398 | |||||
| chr13:45513400
|
C | CATAATAT others(17): Show |
3 | a0001c0002t0001g0204a0001c0002t0001g0281a0001c0002t0001g0312 | 3 | HG02145.hp2 NA18977.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1809+1549_1809+155 others(28): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513400 | |||||
| chr13:45513400
|
C | T | 27 | a0001c0002t0001g0146a0001c0002t0001g0147a0002c0004t0001g0001others(24): Show | 31 | HG00408.hp1 HG01256.hp1 HG01258.hp1 others(28): Show |
intron_variant | MODIFIER | c.1809+1546C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513400 | ||||||
| chr13:45513400
|
CAT | C | 91 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(88): Show | 93 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1809+1550_1809+155 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513400 | |||||
| chr13:45513421
|
TTA | T | 3 | a0001c0002t0001g0257a0001c0014t0001g0261a0002c0005t0014g0206 | 3 | HG03225.hp1 HG04204.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.1809+1576_1809+157 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513421 | |||||
| chr13:45513422
|
T | C | 97 | a0001c0001t0001g0113a0001c0002t0001g0008a0001c0002t0001g0009others(94): Show | 99 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1809+1568T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513422 | ||||||
| chr13:45513422
|
T | TATATATA others(67): Show |
8 | a0003c0006t0004g0193a0003c0006t0004g0195a0003c0006t0004g0196others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1809+1575_1809+157 others(78): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513422 | |||||
| chr13:45513422
|
T | TATATATA others(93): Show |
1 | a0001c0013t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1809+1575_1809+157 others(104): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513422 | |||||
| chr13:45513426
|
T | C | 67 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(64): Show | 70 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1809+1572T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513426 | ||||||
| chr13:45513428
|
T | C | 2 | a0001c0002t0001g0257a0001c0014t0001g0261 | 2 | HG04204.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.1809+1574T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513428 | ||||||
| chr13:45513447
|
TTA | T | 67 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(64): Show | 70 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1809+1602_1809+160 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513447 | |||||
| chr13:45513448
|
T | C | 220 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1809+1594T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513448 | ||||||
| chr13:45513449
|
A | ATATATAT others(13): Show |
1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1809+1606_1809+160 others(24): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513449 | |||||
| chr13:45513473
|
TTA | T | 3 | a0001c0002t0001g0281a0001c0002t0001g0312a0001c0013t0004g0194 | 3 | HG02145.hp2 HG03139.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1809+1628_1809+162 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513473 | |||||
| chr13:45513474
|
T | C | 216 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.1809+1620T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513474 | ||||||
| chr13:45513478
|
T | C | 67 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(64): Show | 70 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1809+1624T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513478 | ||||||
| chr13:45513493
|
T | A | 3 | a0001c0002t0001g0009a0001c0002t0001g0276a0001c0002t0001g0314 | 4 | NA18971.hp2 NA18987.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1809+1639T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513493 | ||||||
| chr13:45513498
|
A | G | 1 | a0001c0002t0001g0272 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1809+1644A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513498 | ||||||
| chr13:45513499
|
TTA | T | 282 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(279): Show | 288 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.1809+1654_1809+165 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513499 | |||||
| chr13:45513500
|
T | C | 1 | a0001c0014t0001g0261 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1809+1646T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513500 | ||||||
| chr13:45513520
|
A | G | 1 | a0002c0004t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1809+1666A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513520 | ||||||
| chr13:45513543
|
C | T | 4 | a0001c0001t0001g0113a0001c0001t0001g0124a0001c0001t0001g0131others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1809+1689C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513543 | ||||||
| chr13:45513555
|
A | G | 68 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(65): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1809+1701A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513555 | ||||||
| chr13:45513562
|
A | ATATATAC others(19): Show |
2 | a0002c0005t0003g0004a0002c0005t0003g0155 | 3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1809+1708_1809+170 others(30): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513562 | ||||||
| chr13:45513642
|
G | A | 220 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1809+1788G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513642 | ||||||
| chr13:45513646
|
C | G | 9 | a0001c0013t0004g0194a0003c0006t0004g0193a0003c0006t0004g0195others(6): Show | 9 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1809+1792C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513646 | ||||||
| chr13:45513762
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0125 | 2 | HG02056.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1809+1908G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513762 | ||||||
| chr13:45513865
|
T | C | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1809+2011T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513865 | ||||||
| chr13:45513986
|
T | C | 36 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(33): Show | 38 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.1809+2132T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513986 | ||||||
| chr13:45514157
|
C | CT | 49 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0072others(46): Show | 52 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.1810-1965dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45514157 | |||||
| chr13:45514157
|
C | CTT | 151 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(148): Show | 153 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.1810-1966_1810-196 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45514157 | |||||
| chr13:45514157
|
C | CTTT | 92 | a0001c0001t0001g0069a0001c0001t0001g0078a0001c0001t0001g0082others(89): Show | 94 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1810-1967_1810-196 others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45514157 | |||||
| chr13:45514157
|
C | CTTTT | 8 | a0001c0002t0001g0269a0001c0002t0001g0290a0001c0002t0001g0298others(5): Show | 8 | HG00741.hp1 HG01106.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1810-1968_1810-196 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45514157 | |||||
| chr13:45514208
|
T | C | 1 | a0002c0007t0002g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1810-1935T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514208 | ||||||
| chr13:45514315
|
C | T | 68 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(65): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1810-1828C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514315 | ||||||
| chr13:45514317
|
C | T | 2 | a0002c0005t0003g0004a0002c0005t0003g0155 | 3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1810-1826C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514317 | ||||||
| chr13:45514440
|
A | C | 330 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(327): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.1810-1703A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514440 | ||||||
| chr13:45514493
|
G | A | 289 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1810-1650G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514493 | ||||||
| chr13:45514708
|
C | G | 2 | a0002c0004t0001g0031a0002c0004t0001g0034 | 2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1810-1435C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514708 | ||||||
| chr13:45514792
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1810-1351C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514792 | ||||||
| chr13:45514867
|
C | T | 2 | a0001c0002t0001g0229a0001c0002t0001g0230 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1810-1276C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514867 | ||||||
| chr13:45514903
|
C | T | 2 | a0002c0005t0003g0004a0002c0005t0003g0155 | 3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1810-1240C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514903 | ||||||
| chr13:45514928
|
G | A | 1 | a0002c0004t0010g0025 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1810-1215G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514928 | ||||||
| chr13:45514951
|
C | T | 68 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(65): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1810-1192C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514951 | ||||||
| chr13:45515058
|
A | C | 2 | a0001c0002t0001g0302a0001c0002t0001g0312 | 2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1810-1085A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515058 | ||||||
| chr13:45515062
|
A | G | 3 | a0001c0001t0001g0120a0001c0001t0001g0129a0001c0001t0001g0145 | 3 | HG02080.hp1 HG02165.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1810-1081A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515062 | ||||||
| chr13:45515126
|
A | T | 289 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1810-1017A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515126 | ||||||
| chr13:45515260
|
T | C | 96 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(93): Show | 98 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1810-883T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515260 | ||||||
| chr13:45515299
|
G | A | 4 | a0001c0002t0001g0008a0001c0002t0001g0242a0001c0002t0001g0243others(1): Show | 5 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1810-844G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515299 | ||||||
| chr13:45515388
|
A | G | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1810-755A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515388 | ||||||
| chr13:45515446
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1810-697C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515446 | ||||||
| chr13:45515532
|
C | T | 68 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(65): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1810-611C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515532 | ||||||
| chr13:45515545
|
A | G | 68 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(65): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1810-598A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515545 | ||||||
| chr13:45515709
|
A | G | 15 | a0002c0003t0002g0208a0002c0003t0002g0209a0002c0003t0002g0210others(12): Show | 15 | HG01109.hp2 HG01361.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.1810-434A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515709 | ||||||
| chr13:45515734
|
C | G | 1 | a0001c0002t0001g0321 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1810-409C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515734 | ||||||
| chr13:45515774
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1810-369G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515774 | ||||||
| chr13:45515782
|
T | C | 96 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(93): Show | 98 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1810-361T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515782 | ||||||
| chr13:45515824
|
A | T | 69 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(66): Show | 72 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.1810-319A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515824 | ||||||
| chr13:45516098
|
T | A | 1 | a0002c0003t0002g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1810-45T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45516098 | ||||||
| chr13:45516420
|
C | T | 2 | a0002c0003t0002g0184a0002c0003t0002g0185 | 2 | NA18939.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1930+157C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45516420 | ||||||
| chr13:45516422
|
A | G | 1 | a0002c0003t0002g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1930+159A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45516422 | ||||||
| chr13:45516551
|
A | G | 2 | a0002c0005t0011g0150a0002c0005t0012g0148 | 2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1930+288A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45516551 | ||||||
| chr13:45516635
|
G | A | 1 | a0002c0003t0002g0171 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1930+372G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45516635 | ||||||
| chr13:45516684
|
G | A | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1930+421G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45516684 | ||||||
| chr13:45516807
|
T | G | 4 | a0002c0005t0003g0157a0002c0005t0003g0158a0002c0005t0003g0159others(1): Show | 4 | HG00408.hp1 HG02015.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1930+544T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45516807 | ||||||
| chr13:45516893
|
T | G | 1 | a0001c0001t0001g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1930+630T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45516893 | ||||||
| chr13:45517033
|
G | T | 1 | a0001c0001t0001g0100 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1930+770G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517033 | ||||||
| chr13:45517228
|
T | C | 235 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(232): Show | 239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1930+965T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517228 | ||||||
| chr13:45517232
|
C | T | 23 | a0002c0003t0002g0202a0002c0003t0002g0208a0002c0003t0002g0209others(20): Show | 23 | HG01074.hp2 HG01109.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1930+969C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517232 | ||||||
| chr13:45517250
|
T | C | 4 | a0002c0005t0003g0157a0002c0005t0003g0158a0002c0005t0003g0159others(1): Show | 4 | HG00408.hp1 HG02015.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1930+987T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517250 | ||||||
| chr13:45517385
|
T | C | 235 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(232): Show | 239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1930+1122T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517385 | ||||||
| chr13:45517501
|
A | T | 1 | a0001c0002t0001g0245 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1930+1238A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517501 | ||||||
| chr13:45517554
|
G | C | 1 | a0001c0001t0001g0100 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1931-1208G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517554 | ||||||
| chr13:45517557
|
T | TTGGTTTG others(314): Show |
4 | a0002c0005t0003g0151a0002c0005t0003g0152a0002c0005t0003g0153others(1): Show | 4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1931-1198_1931-119 others(325): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 45517557 | |||||
| chr13:45517587
|
C | T | 235 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(232): Show | 239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1931-1175C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517587 | ||||||
| chr13:45517690
|
G | C | 1 | a0002c0003t0002g0236 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1931-1072G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517690 | ||||||
| chr13:45517918
|
T | A | 1 | a0002c0003t0002g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1931-844T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517918 | ||||||
| chr13:45517987
|
T | C | 222 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(219): Show | 225 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.1931-775T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517987 | ||||||
| chr13:45518126
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1931-636A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45518126 | ||||||
| chr13:45518190
|
A | G | 12 | a0002c0005t0003g0004a0002c0005t0003g0010a0002c0005t0003g0151others(9): Show | 13 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1931-572A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45518190 | ||||||
| chr13:45518285
|
C | G | 2 | a0001c0002t0001g0229a0001c0002t0001g0230 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1931-477C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45518285 | ||||||
| chr13:45518328
|
C | T | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1931-434C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45518328 | ||||||
| chr13:45518555
|
C | T | 1 | a0001c0002t0001g0312 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1931-207C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45518555 | ||||||
| chr13:45518720
|
G | A | 1 | a0002c0003t0002g0234 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1931-42G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45518720 | ||||||
| chr13:45518895
|
T | A | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2019+45T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 18/22 | chr13 | 45518895 | ||||||
| chr13:45519149
|
C | G | 96 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(93): Show | 98 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.2154+55C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45519149 | ||||||
| chr13:45519304
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0078 | 2 | HG01106.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.2154+210G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45519304 | ||||||
| chr13:45519422
|
A | G | 103 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(100): Show | 104 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.2154+328A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45519422 | ||||||
| chr13:45519470
|
G | T | 220 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.2154+376G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45519470 | ||||||
| chr13:45519592
|
A | T | 1 | a0001c0013t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2154+498A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45519592 | ||||||
| chr13:45519637
|
G | C | 1 | a0001c0001t0001g0067 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2154+543G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45519637 | ||||||
| chr13:45519694
|
A | G | 209 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(206): Show | 212 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.2154+600A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45519694 | ||||||
| chr13:45519736
|
G | C | 1 | a0001c0002t0001g0324 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2154+642G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45519736 | ||||||
| chr13:45520108
|
T | G | 4 | a0002c0005t0003g0151a0002c0005t0003g0152a0002c0005t0003g0153others(1): Show | 4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2154+1014T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520108 | ||||||
| chr13:45520131
|
C | T | 88 | a0001c0001t0001g0111a0001c0001t0001g0125a0001c0002t0001g0263others(85): Show | 91 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.2154+1037C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520131 | ||||||
| chr13:45520145
|
C | T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2154+1051C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520145 | ||||||
| chr13:45520157
|
C | T | 5 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(2): Show | 5 | NA18942.hp1 NA18944.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.2154+1063C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520157 | ||||||
| chr13:45520285
|
C | CA | 218 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.2154+1201dupA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45520285 | |||||
| chr13:45520285
|
CA | C | 68 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(65): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2154+1201delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45520285 | |||||
| chr13:45520296
|
T | A | 16 | a0001c0002t0001g0253a0001c0002t0001g0255a0001c0002t0001g0256others(13): Show | 16 | HG02040.hp2 HG02071.hp2 NA18943.hp2 others(13): Show |
intron_variant | MODIFIER | c.2154+1202T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520296 | ||||||
| chr13:45520312
|
AAT | A | 8 | a0003c0006t0004g0193a0003c0006t0004g0195a0003c0006t0004g0196others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154+1220_2154+122 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45520312 | |||||
| chr13:45520318
|
A | G | 8 | a0003c0006t0004g0193a0003c0006t0004g0195a0003c0006t0004g0196others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154+1224A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520318 | ||||||
| chr13:45520320
|
A | G | 8 | a0003c0006t0004g0193a0003c0006t0004g0195a0003c0006t0004g0196others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154+1226A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520320 | ||||||
| chr13:45520322
|
G | A | 8 | a0003c0006t0004g0193a0003c0006t0004g0195a0003c0006t0004g0196others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154+1228G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520322 | ||||||
| chr13:45520322
|
G | GAGAA | 295 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.2154+1238_2154+124 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45520322 | |||||
| chr13:45520527
|
A | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.2154+1433A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520527 | ||||||
| chr13:45520678
|
G | A | 232 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(229): Show | 236 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.2154+1584G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520678 | ||||||
| chr13:45520678
|
G | C | 3 | a0001c0002t0001g0229a0001c0002t0001g0230a0002c0003t0002g0240 | 3 | HG02922.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2154+1584G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520678 | ||||||
| chr13:45520703
|
A | AT | 221 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(218): Show | 224 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.2154+1616dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45520703 | |||||
| chr13:45520971
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2154+1877A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520971 | ||||||
| chr13:45521054
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2154+1960C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521054 | ||||||
| chr13:45521158
|
A | AT | 38 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(35): Show | 40 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.2154+2074dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521158 | |||||
| chr13:45521371
|
C | G | 2 | a0001c0002t0001g0229a0001c0002t0001g0230 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2154+2277C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521371 | ||||||
| chr13:45521419
|
C | T | 2 | a0002c0005t0003g0010a0002c0005t0003g0192 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2154+2325C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521419 | ||||||
| chr13:45521424
|
TC | T | 37 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(34): Show | 39 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.2154+2331delC | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521424 | ||||||
| chr13:45521550
|
G | A | 1 | a0001c0013t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2154+2456G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521550 | ||||||
| chr13:45521577
|
G | GCA | 5 | a0001c0001t0001g0099a0001c0001t0001g0119a0001c0001t0001g0143others(2): Show | 5 | HG02071.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.2154+2507_2154+250 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521577 | |||||
| chr13:45521577
|
G | GCACA | 46 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(43): Show | 52 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.2154+2505_2154+250 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521577 | |||||
| chr13:45521577
|
G | GCACACA | 24 | a0002c0003t0002g0202a0002c0003t0002g0208a0002c0003t0002g0210others(21): Show | 24 | HG01109.hp2 HG01192.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.2154+2503_2154+250 others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521577 | |||||
| chr13:45521577
|
G | GCACACAC others(1): Show |
23 | a0002c0003t0002g0209a0002c0003t0002g0233a0002c0003t0002g0234others(20): Show | 23 | HG00280.hp1 HG00597.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.2154+2501_2154+250 others(12): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521577 | |||||
| chr13:45521577
|
G | GCACACAC others(3): Show |
5 | a0002c0003t0002g0007a0002c0003t0002g0235a0002c0005t0003g0152others(2): Show | 6 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.2154+2499_2154+250 others(14): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521577 | |||||
| chr13:45521577
|
G | GCACACAC others(5): Show |
4 | a0002c0005t0003g0004a0002c0005t0003g0151a0002c0005t0003g0155others(1): Show | 5 | HG00639.hp1 HG01243.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2154+2497_2154+250 others(16): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521577 | |||||
| chr13:45521577
|
G | GCACACAC others(9): Show |
1 | a0002c0005t0003g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2154+2493_2154+250 others(20): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521577 | |||||
| chr13:45521577
|
G | GCGCACAC others(5): Show |
1 | a0002c0016t0003g0156 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2154+2484_2154+248 others(16): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521577 | |||||
| chr13:45521577
|
GCA | G | 9 | a0002c0005t0014g0206a0003c0006t0004g0193a0003c0006t0004g0195others(6): Show | 9 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2154+2507_2154+250 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521577 | |||||
| chr13:45521577
|
GCACACAC others(5): Show |
G | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2154+2497_2154+250 others(16): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521577 | |||||
| chr13:45521655
|
T | A | 1 | a0001c0001t0001g0083 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2154+2561T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521655 | ||||||
| chr13:45521717
|
A | G | 1 | a0002c0004t0001g0030 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2154+2623A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521717 | ||||||
| chr13:45521802
|
CTT | C | 69 | a0001c0001t0001g0141a0002c0003t0002g0005a0002c0003t0002g0006others(66): Show | 72 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.2154+2727_2154+272 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521802 | |||||
| chr13:45521802
|
CTTT | C | 215 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(212): Show | 218 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.2154+2726_2154+272 others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521802 | |||||
| chr13:45521845
|
T | C | 303 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(300): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.2154+2751T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521845 | ||||||
| chr13:45521886
|
T | C | 16 | a0001c0002t0001g0253a0001c0002t0001g0255a0001c0002t0001g0256others(13): Show | 16 | HG02040.hp2 HG02071.hp2 NA18943.hp2 others(13): Show |
intron_variant | MODIFIER | c.2154+2792T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521886 | ||||||
| chr13:45521925
|
C | T | 10 | a0002c0004t0001g0001a0002c0004t0001g0002a0002c0004t0001g0016others(7): Show | 14 | HG02074.hp1 HG02129.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.2154+2831C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521925 | ||||||
| chr13:45521958
|
G | A | 68 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(65): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2154+2864G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521958 | ||||||
| chr13:45522078
|
A | T | 330 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(327): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.2155-2898A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45522078 | ||||||
| chr13:45522174
|
A | G | 221 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(218): Show | 224 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.2155-2802A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45522174 | ||||||
| chr13:45522218
|
C | T | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2155-2758C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45522218 | ||||||
| chr13:45522237
|
G | A | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2155-2739G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45522237 | ||||||
| chr13:45522494
|
A | T | 23 | a0002c0003t0002g0202a0002c0003t0002g0208a0002c0003t0002g0209others(20): Show | 23 | HG01074.hp2 HG01109.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.2155-2482A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45522494 | ||||||
| chr13:45522572
|
G | C | 69 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(66): Show | 72 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.2155-2404G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45522572 | ||||||
| chr13:45522726
|
G | A | 304 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(301): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.2155-2250G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45522726 | ||||||
| chr13:45522754
|
C | T | 14 | a0002c0005t0003g0004a0002c0005t0003g0010a0002c0005t0003g0151others(11): Show | 15 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.2155-2222C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45522754 | ||||||
| chr13:45522888
|
G | A | 11 | a0002c0005t0003g0004a0002c0005t0003g0010a0002c0005t0003g0151others(8): Show | 12 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2155-2088G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45522888 | ||||||
| chr13:45522940
|
G | T | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2155-2036G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45522940 | ||||||
| chr13:45523033
|
G | T | 96 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(93): Show | 98 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.2155-1943G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45523033 | ||||||
| chr13:45523076
|
G | T | 1 | a0001c0002t0001g0323 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2155-1900G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45523076 | ||||||
| chr13:45523077
|
C | G | 1 | a0001c0002t0001g0323 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2155-1899C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45523077 | ||||||
| chr13:45523078
|
T | C | 1 | a0001c0002t0001g0323 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2155-1898T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45523078 | ||||||
| chr13:45523149
|
GT | G | 213 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(210): Show | 216 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.2155-1813delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45523149 | |||||
| chr13:45523149
|
GTT | G | 20 | a0001c0002t0001g0273a0001c0002t0001g0274a0001c0002t0001g0290others(17): Show | 21 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.2155-1814_2155-181 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45523149 | |||||
| chr13:45523227
|
A | T | 1 | a0002c0003t0002g0174 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2155-1749A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45523227 | ||||||
| chr13:45523510
|
TA | T | 5 | a0003c0006t0004g0195a0003c0006t0004g0196a0003c0006t0004g0197others(2): Show | 5 | HG02559.hp2 HG02717.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2155-1459delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45523510 | |||||
| chr13:45523748
|
A | G | 3 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0001g0149 | 3 | NA18939.hp1 NA18943.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.2155-1228A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45523748 | ||||||
| chr13:45523976
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2155-1000G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45523976 | ||||||
| chr13:45524057
|
A | G | 182 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(179): Show | 186 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.2155-919A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45524057 | ||||||
| chr13:45524301
|
CCCATAGC others(4): Show |
C | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2155-671_2155-661d others(13): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45524301 | |||||
| chr13:45524408
|
A | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0118 | 2 | NA18966.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2155-568A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45524408 | ||||||
| chr13:45524410
|
G | T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2155-566G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45524410 | ||||||
| chr13:45524540
|
G | A | 1 | a0002c0003t0002g0160 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2155-436G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45524540 | ||||||
| chr13:45524593
|
T | C | 31 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(28): Show | 33 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.2155-383T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45524593 | ||||||
| chr13:45524780
|
T | C | 11 | a0002c0005t0003g0004a0002c0005t0003g0010a0002c0005t0003g0151others(8): Show | 12 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2155-196T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45524780 | ||||||
| chr13:45524820
|
AT | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(100): Show | 104 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.2155-148delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45524820 | |||||
| chr13:45524859
|
T | C | 219 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.2155-117T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45524859 | ||||||
| chr13:45524966
|
C | T | 1 | a0001c0002t0001g0262 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2155-10C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45524966 | ||||||
| chr13:45524972
|
T | C | 2 | a0002c0005t0003g0010a0002c0005t0003g0192 | 2 | HG02723.hp1 HG03471.hp2 |
splice_region_variant&intron_variant | LOW | c.2155-4T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45524972 | ||||||
| chr13:45525108
|
A | G | 221 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(218): Show | 224 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.2230+57A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525108 | ||||||
| chr13:45525132
|
G | A | 2 | a0002c0005t0011g0150a0002c0005t0012g0148 | 2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2230+81G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525132 | ||||||
| chr13:45525213
|
G | A | 5 | a0002c0003t0002g0169a0002c0003t0002g0171a0002c0003t0002g0174others(2): Show | 5 | HG00609.hp1 HG02056.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.2230+162G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525213 | ||||||
| chr13:45525401
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2230+350G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525401 | ||||||
| chr13:45525471
|
T | C | 1 | a0002c0004t0001g0012 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2230+420T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525471 | ||||||
| chr13:45525481
|
A | G | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2230+430A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525481 | ||||||
| chr13:45525582
|
C | CTTAAATG others(6): Show |
94 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(91): Show | 96 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.2230+531_2230+532i others(15): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525582 | ||||||
| chr13:45525583
|
C | T | 94 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(91): Show | 96 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.2230+532C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525583 | ||||||
| chr13:45525584
|
C | A | 94 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(91): Show | 96 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.2230+533C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525584 | ||||||
| chr13:45525633
|
G | GTTTTTTT others(9): Show |
1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2230+582_2230+583i others(18): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525633 | ||||||
| chr13:45525634
|
G | GT | 11 | a0002c0004t0001g0001a0002c0004t0001g0002a0002c0004t0001g0012others(8): Show | 15 | HG00597.hp1 HG02015.hp2 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.2230+601dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45525634 | |||||
| chr13:45525634
|
G | GTTTTTTT | 8 | a0001c0002t0001g0249a0001c0002t0007g0305a0002c0003t0002g0217others(5): Show | 8 | HG00738.hp1 HG01074.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.2230+595_2230+601d others(9): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45525634 | |||||
| chr13:45525634
|
G | GTTTTTTT others(1): Show |
106 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(103): Show | 110 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.2230+594_2230+601d others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45525634 | |||||
| chr13:45525634
|
G | GTTTTTTT others(2): Show |
54 | a0001c0002t0001g0229a0001c0002t0001g0230a0001c0002t0001g0245others(51): Show | 56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.2230+593_2230+601d others(11): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45525634 | |||||
| chr13:45525634
|
G | GTTTTTTT others(3): Show |
20 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037others(17): Show | 20 | HG02056.hp2 HG02257.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.2230+592_2230+601d others(12): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45525634 | |||||
| chr13:45525634
|
G | GTTTTTTT others(4): Show |
3 | a0001c0001t0001g0122a0002c0003t0002g0180a0002c0016t0003g0156 | 3 | HG01981.hp1 HG02922.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2230+591_2230+601d others(13): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45525634 | |||||
| chr13:45525634
|
G | GTTTTTTT others(5): Show |
77 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0043others(74): Show | 78 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.2230+590_2230+601d others(14): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45525634 | |||||
| chr13:45525634
|
G | GTTTTTTT others(6): Show |
22 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0059others(19): Show | 22 | HG00438.hp1 HG00639.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.2230+589_2230+601d others(15): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45525634 | |||||
| chr13:45525634
|
G | GTTTTTTT others(7): Show |
8 | a0001c0001t0001g0067a0001c0001t0001g0095a0001c0001t0001g0114others(5): Show | 8 | HG01261.hp2 HG02080.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2230+588_2230+601d others(16): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45525634 | |||||
| chr13:45525634
|
G | T | 2 | a0002c0005t0011g0150a0002c0005t0012g0148 | 2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2230+583G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525634 | ||||||
| chr13:45525693
|
T | A | 1 | a0002c0004t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2230+642T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525693 | ||||||
| chr13:45525695
|
A | G | 1 | a0002c0004t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2230+644A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525695 | ||||||
| chr13:45525798
|
T | TAGAG | 301 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(298): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.2230+749_2230+750i others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45525798 | |||||
| chr13:45525912
|
G | T | 6 | a0002c0003t0002g0233a0002c0003t0002g0234a0002c0003t0002g0235others(3): Show | 6 | HG01074.hp2 HG02622.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2230+861G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525912 | ||||||
| chr13:45526076
|
A | AT | 10 | a0002c0004t0001g0002a0002c0004t0001g0013a0002c0004t0001g0014others(7): Show | 12 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.2230+1055dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | |||||
| chr13:45526076
|
A | ATT | 16 | a0001c0002t0001g0205a0001c0002t0001g0229a0001c0002t0001g0230others(13): Show | 18 | HG00642.hp2 HG02074.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2230+1054_2230+105 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | |||||
| chr13:45526076
|
A | ATTT | 23 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0098others(20): Show | 24 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.2230+1053_2230+105 others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | |||||
| chr13:45526076
|
A | ATTTT | 76 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0044others(73): Show | 77 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.2230+1052_2230+105 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | |||||
| chr13:45526076
|
A | ATTTTT | 78 | a0001c0001t0001g0043a0001c0001t0001g0047a0001c0001t0001g0052others(75): Show | 78 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.2230+1051_2230+105 others(9): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | |||||
| chr13:45526076
|
A | ATTTTTT | 17 | a0001c0001t0001g0054a0001c0001t0001g0076a0001c0001t0001g0097others(14): Show | 18 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.2230+1050_2230+105 others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | |||||
| chr13:45526076
|
A | ATTTTTTT | 8 | a0001c0001t0001g0041a0001c0001t0001g0059a0001c0001t0001g0082others(5): Show | 8 | HG00408.hp2 HG00438.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2230+1049_2230+105 others(11): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | |||||
| chr13:45526076
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0117 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2230+1045_2230+105 others(15): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | |||||
| chr13:45526076
|
AT | A | 6 | a0002c0004t0001g0038a0002c0005t0003g0151a0002c0005t0003g0152others(3): Show | 6 | HG02615.hp1 HG02965.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2230+1055delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | |||||
| chr13:45526076
|
ATT | A | 6 | a0001c0001t0001g0133a0002c0005t0003g0004a0002c0005t0003g0158others(3): Show | 7 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.2230+1054_2230+105 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | |||||
| chr13:45526076
|
ATTTT | A | 32 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0144others(29): Show | 34 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.2230+1052_2230+105 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | |||||
| chr13:45526076
|
ATTTTTT | A | 27 | a0002c0003t0002g0007a0002c0003t0002g0202a0002c0003t0002g0208others(24): Show | 28 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.2230+1050_2230+105 others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | |||||
| chr13:45526076
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2230+1046_2230+105 others(14): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | |||||
| chr13:45526076
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0107 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2230+1045_2230+105 others(15): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | |||||
| chr13:45526076
|
ATTTTTTT others(6): Show |
A | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2230+1043_2230+105 others(17): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | |||||
| chr13:45526076
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0115 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2230+1042_2230+105 others(18): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | |||||
| chr13:45526114
|
A | G | 1 | a0002c0003t0002g0186 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2230+1063A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45526114 | ||||||
| chr13:45526158
|
G | A | 67 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(64): Show | 70 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2230+1107G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45526158 | ||||||
| chr13:45526253
|
T | C | 2 | a0001c0002t0001g0304a0001c0002t0007g0305 | 2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.2230+1202T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45526253 | ||||||
| chr13:45526274
|
C | T | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2230+1223C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45526274 | ||||||
| chr13:45526338
|
G | T | 4 | a0001c0001t0001g0133a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 4 | NA18977.hp1 NA18985.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.2230+1287G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45526338 | ||||||
| chr13:45526406
|
T | C | 2 | a0001c0002t0001g0229a0001c0002t0001g0230 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2230+1355T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45526406 | ||||||
| chr13:45526447
|
A | G | 287 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(284): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.2230+1396A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45526447 | ||||||
| chr13:45526637
|
C | G | 94 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(91): Show | 96 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.2230+1586C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45526637 | ||||||
| chr13:45526878
|
T | C | 14 | a0002c0005t0003g0004a0002c0005t0003g0010a0002c0005t0003g0151others(11): Show | 15 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.2230+1827T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45526878 | ||||||
| chr13:45526879
|
C | T | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2230+1828C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45526879 | ||||||
| chr13:45527220
|
A | T | 16 | a0001c0002t0001g0253a0001c0002t0001g0255a0001c0002t0001g0256others(13): Show | 16 | HG02040.hp2 HG02071.hp2 NA18943.hp2 others(13): Show |
intron_variant | MODIFIER | c.2230+2169A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45527220 | ||||||
| chr13:45527258
|
T | C | 95 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(92): Show | 97 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.2230+2207T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45527258 | ||||||
| chr13:45527263
|
G | C | 2 | a0001c0001t0001g0056a0001c0001t0001g0066 | 2 | HG00741.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.2230+2212G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45527263 | ||||||
| chr13:45527426
|
G | A | 67 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(64): Show | 70 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2231-2365G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45527426 | ||||||
| chr13:45527429
|
G | A | 67 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(64): Show | 70 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2231-2362G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45527429 | ||||||
| chr13:45527447
|
A | G | 2 | a0002c0005t0003g0004a0002c0005t0003g0155 | 3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2231-2344A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45527447 | ||||||
| chr13:45527865
|
T | A | 1 | a0002c0003t0002g0160 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2231-1926T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45527865 | ||||||
| chr13:45527925
|
C | G | 1 | a0001c0002t0001g0245 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2231-1866C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45527925 | ||||||
| chr13:45528018
|
T | C | 301 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(298): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.2231-1773T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45528018 | ||||||
| chr13:45528097
|
A | C | 69 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(66): Show | 72 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.2231-1694A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45528097 | ||||||
| chr13:45528195
|
A | G | 1 | a0002c0004t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2231-1596A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45528195 | ||||||
| chr13:45528223
|
A | G | 301 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(298): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.2231-1568A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45528223 | ||||||
| chr13:45528293
|
C | T | 14 | a0002c0005t0003g0004a0002c0005t0003g0010a0002c0005t0003g0151others(11): Show | 15 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.2231-1498C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45528293 | ||||||
| chr13:45528418
|
C | G | 107 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(104): Show | 108 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.2231-1373C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45528418 | ||||||
| chr13:45528430
|
G | A | 1 | a0002c0003t0002g0190 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2231-1361G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45528430 | ||||||
| chr13:45528465
|
A | G | 287 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(284): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.2231-1326A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45528465 | ||||||
| chr13:45528599
|
T | C | 1 | a0002c0003t0002g0006 | 2 | NA19002.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2231-1192T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45528599 | ||||||
| chr13:45528955
|
G | T | 1 | a0002c0005t0003g0155 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2231-836G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45528955 | ||||||
| chr13:45529002
|
A | G | 12 | a0002c0005t0003g0004a0002c0005t0003g0010a0002c0005t0003g0151others(9): Show | 13 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.2231-789A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45529002 | ||||||
| chr13:45529058
|
C | G | 1 | a0001c0002t0001g0258 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2231-733C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45529058 | ||||||
| chr13:45529094
|
C | G | 1 | a0002c0003t0002g0188 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2231-697C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45529094 | ||||||
| chr13:45529138
|
C | T | 1 | a0001c0002t0001g0258 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2231-653C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45529138 | ||||||
| chr13:45529207
|
A | G | 69 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(66): Show | 72 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.2231-584A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45529207 | ||||||
| chr13:45529443
|
A | ACTAGTGT | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2231-345_2231-339d others(9): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45529443 | |||||
| chr13:45529465
|
CT | C | 70 | a0001c0001t0001g0062a0002c0003t0002g0005a0002c0003t0002g0006others(67): Show | 73 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.2231-314delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45529465 | |||||
| chr13:45529722
|
C | T | 1 | a0002c0003t0002g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2231-69C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45529722 | ||||||
| chr13:45529995
|
G | C | 287 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(284): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.2358+77G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/22 | chr13 | 45529995 | ||||||
| chr13:45530189
|
G | A | 218 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.2358+271G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/22 | chr13 | 45530189 | ||||||
| chr13:45530266
|
G | A | 1 | a0002c0005t0013g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2358+348G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/22 | chr13 | 45530266 | ||||||
| chr13:45530281
|
C | G | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2358+363C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/22 | chr13 | 45530281 | ||||||
| chr13:45530312
|
C | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(106): Show | 110 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.2359-370C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/22 | chr13 | 45530312 | ||||||
| chr13:45530400
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2359-282T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/22 | chr13 | 45530400 | ||||||
| chr13:45530401
|
G | A | 301 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(298): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.2359-281G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/22 | chr13 | 45530401 | ||||||
| chr13:45530458
|
A | G | 9 | a0001c0013t0004g0194a0003c0006t0004g0193a0003c0006t0004g0195others(6): Show | 9 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2359-224A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/22 | chr13 | 45530458 | ||||||
| chr13:45530528
|
C | T | 286 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(283): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.2359-154C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/22 | chr13 | 45530528 | ||||||
| chr13:45530886
|
AT | A | 95 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(92): Show | 97 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.2457+107delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45530886 | ||||||
| chr13:45531107
|
TAAG | T | 68 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(65): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2457+329_2457+331d others(5): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr13 | 45531107 | |||||
| chr13:45531454
|
A | G | 1 | a0002c0005t0013g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2457+674A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45531454 | ||||||
| chr13:45531504
|
G | GT | 217 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(214): Show | 220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.2457+729dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr13 | 45531504 | |||||
| chr13:45531510
|
G | T | 300 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(297): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.2457+730G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45531510 | ||||||
| chr13:45531543
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2457+763T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45531543 | ||||||
| chr13:45531548
|
C | T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2457+768C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45531548 | ||||||
| chr13:45531641
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2457+861A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45531641 | ||||||
| chr13:45531912
|
C | T | 1 | a0002c0003t0002g0167 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2457+1132C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45531912 | ||||||
| chr13:45531936
|
A | G | 49 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0204others(46): Show | 51 | HG00099.hp2 HG00544.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.2457+1156A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45531936 | ||||||
| chr13:45532385
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2457+1605A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532385 | ||||||
| chr13:45532393
|
T | G | 2 | a0001c0002t0001g0229a0001c0002t0001g0230 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2457+1613T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532393 | ||||||
| chr13:45532462
|
T | C | 12 | a0002c0005t0003g0004a0002c0005t0003g0010a0002c0005t0003g0151others(9): Show | 13 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.2457+1682T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532462 | ||||||
| chr13:45532486
|
C | T | 15 | a0002c0003t0002g0208a0002c0003t0002g0209a0002c0003t0002g0210others(12): Show | 15 | HG01109.hp2 HG01361.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.2457+1706C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532486 | ||||||
| chr13:45532560
|
G | GT | 7 | a0001c0001t0001g0141a0002c0004t0001g0015a0002c0004t0001g0024others(4): Show | 8 | HG00639.hp1 HG01243.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.2457+1807dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr13 | 45532560 | |||||
| chr13:45532560
|
GT | G | 108 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0043others(105): Show | 109 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.2457+1807delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr13 | 45532560 | |||||
| chr13:45532560
|
GTT | G | 61 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0072others(58): Show | 64 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2457+1806_2457+180 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr13 | 45532560 | |||||
| chr13:45532560
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0001g0102 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2457+1797_2457+180 others(15): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr13 | 45532560 | |||||
| chr13:45532560
|
GTTTTTTT others(6): Show |
G | 95 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0203others(92): Show | 97 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.2457+1795_2457+180 others(17): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr13 | 45532560 | |||||
| chr13:45532575
|
T | G | 1 | a0002c0003t0002g0181 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2457+1795T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532575 | ||||||
| chr13:45532601
|
G | A | 1 | a0001c0002t0001g0325 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2457+1821G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532601 | ||||||
| chr13:45532641
|
C | T | 68 | a0002c0003t0002g0005a0002c0003t0002g0006a0002c0003t0002g0007others(65): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2457+1861C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532641 | ||||||
| chr13:45532652
|
C | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(106): Show | 110 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.2457+1872C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532652 | ||||||
| chr13:45532656
|
G | A | 1 | a0001c0002t0001g0291 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2457+1876G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532656 | ||||||
| chr13:45532791
|
G | T | 301 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(298): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.2458-1911G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532791 | ||||||
| chr13:45532803
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2458-1899C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532803 | ||||||
| chr13:45532813
|
TC | T | 2 | a0002c0005t0003g0004a0002c0005t0003g0155 | 3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2458-1886delC | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr13 | 45532813 | |||||
| chr13:45533012
|
G | A | 1 | a0002c0003t0002g0207 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2458-1690G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533012 | ||||||
| chr13:45533039
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1663G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533039 | ||||||
| chr13:45533040
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1662G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533040 | ||||||
| chr13:45533042
|
C | T | 217 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(214): Show | 220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.2458-1660C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533042 | ||||||
| chr13:45533043
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1659G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533043 | ||||||
| chr13:45533044
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1658A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533044 | ||||||
| chr13:45533045
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1657G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533045 | ||||||
| chr13:45533047
|
G | C | 2 | a0001c0001t0001g0086a0001c0001t0001g0127 | 2 | HG01433.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.2458-1655G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533047 | ||||||
| chr13:45533048
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1654T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533048 | ||||||
| chr13:45533055
|
ATGGATGG others(4): Show |
A | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1644_2458-163 others(15): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr13 | 45533055 | |||||
| chr13:45533088
|
T | C | 1 | a0002c0005t0013g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2458-1614T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533088 | ||||||
| chr13:45533090
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1612G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533090 | ||||||
| chr13:45533091
|
A | T | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1611A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533091 | ||||||
| chr13:45533095
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1607G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533095 | ||||||
| chr13:45533110
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1592T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533110 | ||||||
| chr13:45533111
|
C | A | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1591C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533111 | ||||||
| chr13:45533112
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2458-1590A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533112 | ||||||
| chr13:45533112
|
A | T | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1590A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533112 | ||||||
| chr13:45533114
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1588G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533114 | ||||||
| chr13:45533115
|
T | G | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1587T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533115 | ||||||
| chr13:45533144
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1558C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533144 | ||||||
| chr13:45533148
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1554G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533148 | ||||||
| chr13:45533151
|
A | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1551A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533151 | ||||||
| chr13:45533152
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1550G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533152 | ||||||
| chr13:45533153
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1549G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533153 | ||||||
| chr13:45533154
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1548G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533154 | ||||||
| chr13:45533156
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1546G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533156 | ||||||
| chr13:45533157
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1545G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533157 | ||||||
| chr13:45533158
|
A | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1544A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533158 | ||||||
| chr13:45533160
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1542A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533160 | ||||||
| chr13:45533161
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1541C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533161 | ||||||
| chr13:45533163
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1539G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533163 | ||||||
| chr13:45533181
|
G | A | 1 | a0002c0003t0002g0216 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2458-1521G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533181 | ||||||
| chr13:45533181
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1521G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533181 | ||||||
| chr13:45533203
|
A | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1499A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533203 | ||||||
| chr13:45533267
|
A | C | 9 | a0001c0002t0001g0245a0001c0002t0001g0263a0001c0002t0001g0266others(6): Show | 9 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2458-1435A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533267 | ||||||
| chr13:45533270
|
A | C | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2458-1432A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533270 | ||||||
| chr13:45533615
|
T | C | 1 | a0001c0002t0001g0315 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2458-1087T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533615 | ||||||
| chr13:45533623
|
A | T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2458-1079A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533623 | ||||||
| chr13:45533748
|
A | G | 1 | a0007c0017t0001g0285 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2458-954A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533748 | ||||||
| chr13:45533793
|
C | T | 301 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(298): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.2458-909C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533793 | ||||||
| chr13:45533803
|
C | T | 1 | a0001c0002t0001g0324 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2458-899C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533803 | ||||||
| chr13:45534093
|
C | T | 218 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.2458-609C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45534093 | ||||||
| chr13:45534166
|
C | T | 2 | a0001c0002t0001g0229a0001c0002t0001g0230 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2458-536C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45534166 | ||||||
| chr13:45534179
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2458-523C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45534179 | ||||||
| chr13:45534508
|
T | C | 218 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.2458-194T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45534508 | ||||||
| chr13:45534544
|
A | G | 53 | a0001c0013t0004g0194a0002c0003t0002g0005a0002c0003t0002g0006others(50): Show | 55 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.2458-158A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45534544 | ||||||
| chr13:45534556
|
A | C | 55 | a0001c0013t0004g0194a0002c0003t0002g0005a0002c0003t0002g0006others(52): Show | 57 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.2458-146A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45534556 | ||||||
| chr13:45534568
|
A | T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2458-134A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45534568 | ||||||
| chr13:45534647
|
C | G | 1 | a0001c0014t0001g0261 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2458-55C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45534647 | ||||||
| chr13:45534666
|
A | G | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2458-36A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45534666 |