Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 1495 |
|---|---|
| ensemblid | ENSG00000044115.21 |
| hgncid | 2509 |
| symbol | CTNNA1 |
| name | catenin alpha 1 |
| refseq_nuc | NM_001903.5 |
| refseq_prot | NP_001894.2 |
| ensembl_nuc | ENST00000302763.12 |
| ensembl_prot | ENSP00000304669.7 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 138753425 |
| end | 138935034 |
| strand | + |
| ver | v1.2 |
| region | chr5:138753425-138935034 |
| region5000 | chr5:138748425-138940034 |
| regionname0 | CTNNA1_chr5_138753425_138935034 |
| regionname5000 | CTNNA1_chr5_138748425_138940034 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 906 | 175 | 68 | 42 | 29 | 10 | 24 | 20 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0002 | 0/0 | 906 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0003 | 0/0 | 906 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0004 | 0/0 | 906 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2721 | 106 | 40 | 21 | 28 | 4 | 12 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| c0002 | 0/1 | 2721 | 51 | 19 | 18 | 1 | 3 | 9 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| c0003 | 0/0 | 2721 | 6 | 1 | 2 | 0 | 1 | 2 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| c0004 | 0/0 | 2721 | 3 | 3 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| c0005 | 0/0 | 2721 | 3 | 0 | 1 | 0 | 1 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| c0006 | 0/0 | 2721 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| c0007 | 0/0 | 2721 | 2 | 2 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| c0008 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| c0009 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| c0010 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| c0011 | 0/0 | 2721 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| c0012 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| c0013 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| c0014 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| 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 | 1/0 | 1034 | 112 | 41 | 20 | 31 | 6 | 13 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| t0002 | 0/1 | 1033 | 36 | 4 | 15 | 1 | 4 | 11 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| t0003 | 0/0 | 1030 | 20 | 15 | 5 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| t0004 | 0/0 | 1030 | 4 | 4 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| t0005 | 0/0 | 1033 | 3 | 3 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| t0006 | 0/0 | 1034 | 2 | 2 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| t0007 | 0/0 | 1034 | 2 | 0 | 2 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| t0008 | 0/0 | 1030 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| 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 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0052 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2721 | 106 | 40 | 21 | 28 | 4 | 12 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0002 | 0/1 | 2721 | 51 | 19 | 18 | 1 | 3 | 9 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0003 | 0/0 | 2721 | 6 | 1 | 2 | 0 | 1 | 2 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0004 | 0/0 | 2721 | 3 | 3 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0005 | 0/0 | 2721 | 3 | 0 | 1 | 0 | 1 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0008 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0009 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0011 | 0/0 | 2721 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0012 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0013 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0014 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0002c0006 | 0/0 | 2721 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0003c0007 | 0/0 | 2721 | 2 | 2 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0004c0010 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3754 | 102 | 38 | 19 | 28 | 4 | 12 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0001t0006 | 0/0 | 3754 | 2 | 2 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0001t0007 | 0/0 | 3754 | 2 | 0 | 2 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0002t0002 | 0/1 | 3753 | 30 | 3 | 13 | 1 | 3 | 9 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0002t0003 | 0/0 | 3750 | 17 | 12 | 5 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0002t0005 | 0/0 | 3753 | 3 | 3 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0002t0008 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0003t0002 | 0/0 | 3753 | 6 | 1 | 2 | 0 | 1 | 2 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0004t0004 | 0/0 | 3750 | 3 | 3 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0005t0001 | 0/0 | 3754 | 3 | 0 | 1 | 0 | 1 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0008t0003 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0009t0004 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0011t0001 | 0/0 | 3754 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0012t0003 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0013t0003 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0001c0014t0001 | 0/0 | 3754 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0002c0006t0001 | 0/0 | 3754 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0003c0007t0001 | 0/0 | 3754 | 2 | 2 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| a0004c0010t0001 | 0/0 | 3754 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | copy fasta | chr5 | 138748425 | 138940034 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0052 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0007g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0001t0007g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0002t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0003t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0003t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0003t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0004t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0004t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0004t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0005t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0005t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0005t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0008t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0009t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0011t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0012t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0013t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0001c0014t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0002c0006t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0002c0006t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0003c0007t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0003c0007t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| a0004c0010t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0005 | t0001 | g0167 | EUR | GBR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | GBR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0067 | EUR | FIN | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG00423 | hp2 | a0004 | c0010 | t0001 | g0169 | EAS | CHS | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0066 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG00642 | hp1 | a0001 | c0003 | t0002 | g0055 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0083 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG00741 | hp1 | a0001 | c0002 | t0003 | g0033 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG00741 | hp2 | a0001 | c0005 | t0001 | g0156 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0084 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0075 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0059 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0051 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01099 | hp1 | a0001 | c0001 | t0007 | g0111 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01109 | hp2 | a0001 | c0002 | t0003 | g0024 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01167 | hp2 | a0001 | c0002 | t0003 | g0048 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01168 | hp1 | a0001 | c0001 | t0007 | g0112 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0060 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0056 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0044 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01346 | hp2 | a0001 | c0003 | t0002 | g0064 | AMR | CLM | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0085 | AMR | CLM | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0054 | AMR | CLM | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0053 | EUR | IBS | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | IBS | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01516 | hp1 | a0001 | c0003 | t0002 | g0062 | EUR | IBS | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | IBS | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0069 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0074 | AMR | PEL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01993 | hp1 | a0001 | c0002 | t0003 | g0021 | AMR | PEL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0058 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02280 | hp1 | a0001 | c0012 | t0003 | g0019 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02572 | hp1 | a0001 | c0002 | t0003 | g0047 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0082 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02630 | hp2 | a0001 | c0008 | t0003 | g0030 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02647 | hp1 | a0001 | c0002 | t0005 | g0068 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0057 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02717 | hp2 | a0001 | c0002 | t0003 | g0043 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02723 | hp1 | a0001 | c0002 | t0003 | g0029 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0061 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02738 | hp1 | a0001 | c0003 | t0002 | g0076 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02809 | hp1 | a0001 | c0004 | t0004 | g0180 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02818 | hp1 | a0001 | c0013 | t0003 | g0031 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02818 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02895 | hp1 | a0001 | c0002 | t0005 | g0050 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02895 | hp2 | a0001 | c0002 | t0003 | g0034 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02965 | hp1 | a0001 | c0002 | t0003 | g0049 | AFR | ESN | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02965 | hp2 | a0003 | c0007 | t0001 | g0100 | AFR | ESN | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03139 | hp1 | a0001 | c0014 | t0001 | g0145 | AFR | ESN | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03225 | hp2 | a0001 | c0004 | t0004 | g0005 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03239 | hp2 | a0001 | c0003 | t0002 | g0077 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03453 | hp2 | a0001 | c0002 | t0005 | g0026 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0080 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0027 | AFR | ESN | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0023 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03540 | hp2 | a0001 | c0004 | t0004 | g0007 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03579 | hp1 | a0003 | c0007 | t0001 | g0099 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0081 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03654 | hp2 | a0001 | c0005 | t0001 | g0168 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0071 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0070 | SAS | BEB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0073 | SAS | BEB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0174 | AFR | YRI | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA18906 | hp2 | a0001 | c0002 | t0008 | g0028 | AFR | YRI | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA19043 | hp2 | a0001 | c0002 | t0003 | g0022 | AFR | LWK | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA19057 | hp2 | a0002 | c0006 | t0001 | g0095 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA19060 | hp1 | a0002 | c0006 | t0001 | g0090 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0025 | AFR | YRI | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA20129 | hp2 | a0001 | c0002 | t0003 | g0020 | AFR | ASW | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA20805 | hp1 | a0001 | c0011 | t0001 | g0107 | EUR | TSI | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0079 | EUR | TSI | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | GIH | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0078 | SAS | GIH | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02486 | hp1 | a0001 | c0002 | t0003 | g0032 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02486 | hp2 | a0001 | c0009 | t0004 | g0006 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0035 | AFR | USA | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | USA | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA21309 | hp1 | a0001 | c0003 | t0002 | g0063 | AFR | LWK | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0175 | AFR | LWK | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0065 | REF | REF | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0052 | REF | REF | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:138824596
|
C | T | 1 | a0003 | 2 | HG02965.hp2 HG03579.hp1 |
missense_variant | MODERATE | c.655C>T | p.Pro219Ser | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/18 | 743/3754 | 655/2721 | 219/906 | chr5 | 138824596 | ||
| chr5:138824711
|
A | G | 1 | a0002 | 2 | NA19057.hp2 NA19060.hp1 |
missense_variant | MODERATE | c.770A>G | p.Asn257Ser | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/18 | 858/3754 | 770/2721 | 257/906 | chr5 | 138824711 | ||
| chr5:138925306
|
T | A | 1 | a0004 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.1798T>A | p.Ser600Thr | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/18 | 1886/3754 | 1798/2721 | 600/906 | chr5 | 138925306 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:138812254
|
A | C | 1 | a0001c0003 | 6 | HG00642.hp1 HG01346.hp2 HG01516.hp1 others(3): Show |
synonymous_variant | LOW | c.540A>C | p.Leu180Leu | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/18 | 628/3754 | 540/2721 | 180/906 | chr5 | 138812254 | ||
| chr5:138812260
|
T | G | 3 | a0001c0004a0001c0008a0001c0009 | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
synonymous_variant | LOW | c.546T>G | p.Pro182Pro | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/18 | 634/3754 | 546/2721 | 182/906 | chr5 | 138812260 | ||
| chr5:138917757
|
C | T | 2 | a0001c0004a0001c0009 | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
synonymous_variant | LOW | c.1405C>T | p.Leu469Leu | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/18 | 1493/3754 | 1405/2721 | 469/906 | chr5 | 138917757 | ||
| chr5:138930475
|
G | A | 1 | a0001c0011 | 1 | NA20805.hp1 | splice_region_variant&synonymous_variant | LOW | c.2013G>A | p.Ala671Ala | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 15/18 | 2101/3754 | 2013/2721 | 671/906 | chr5 | 138930475 | ||
| chr5:138930857
|
G | A | 7 | a0001c0002a0001c0003a0001c0004others(4): Show | 64 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(61): Show |
synonymous_variant | LOW | c.2220G>A | p.Ser740Ser | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/18 | 2308/3754 | 2220/2721 | 740/906 | chr5 | 138930857 | ||
| chr5:138930863
|
C | G | 1 | a0001c0005 | 3 | HG00099.hp1 HG00741.hp2 HG03654.hp2 |
synonymous_variant | LOW | c.2226C>G | p.Val742Val | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/18 | 2314/3754 | 2226/2721 | 742/906 | chr5 | 138930863 | ||
| chr5:138932622
|
A | G | 1 | a0001c0014 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.2343A>G | p.Gln781Gln | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 17/18 | 2431/3754 | 2343/2721 | 781/906 | chr5 | 138932622 | ||
| chr5:138933822
|
G | A | 1 | a0001c0012 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.2454G>A | p.Leu818Leu | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 18/18 | 2542/3754 | 2454/2721 | 818/906 | chr5 | 138933822 | ||
| chr5:138933882
|
C | T | 1 | a0001c0009 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.2514C>T | p.Val838Val | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 18/18 | 2602/3754 | 2514/2721 | 838/906 | chr5 | 138933882 | ||
| chr5:138933900
|
A | G | 1 | a0001c0013 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.2532A>G | p.Gln844Gln | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 18/18 | 2620/3754 | 2532/2721 | 844/906 | chr5 | 138933900 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:138753429
|
T | C | 1 | a0001c0002t0008 | 1 | NA18906.hp2 | 5_prime_UTR_variant | MODIFIER | c.-84T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/18 | 28496 | chr5 | 138753429 | |||||
| chr5:138934469
|
C | T | 1 | a0001c0002t0005 | 3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*380C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 18/18 | 380 | chr5 | 138934469 | |||||
| chr5:138934602
|
T | TATC | 3 | a0001c0002t0002a0001c0002t0005a0001c0003t0002 | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*516_*518dupCAT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 18/18 | 519 | INFO_REALIGN_3_PRIME | chr5 | 138934602 | ||||
| chr5:138934749
|
T | C | 1 | a0001c0001t0006 | 2 | NA18522.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*660T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 18/18 | 660 | chr5 | 138934749 | |||||
| chr5:138934799
|
A | G | 1 | a0001c0001t0007 | 2 | HG01099.hp1 HG01168.hp1 |
3_prime_UTR_variant | MODIFIER | c.*710A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 18/18 | 710 | chr5 | 138934799 | |||||
| chr5:138934853
|
T | A | 5 | a0001c0002t0002a0001c0002t0005a0001c0003t0002others(2): Show | 43 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*764T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 18/18 | 764 | chr5 | 138934853 | |||||
| chr5:138934902
|
GTGAT | G | 10 | a0001c0002t0002a0001c0002t0003a0001c0002t0005others(7): Show | 64 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*827_*830delGATT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 18/18 | 827 | INFO_REALIGN_3_PRIME | chr5 | 138934902 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:138753535
|
G | A | 1 | a0001c0001t0001g0001 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-3+25G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138753535 | ||||||
| chr5:138753541
|
G | C | 2 | a0001c0002t0002g0002a0001c0002t0002g0003 | 2 | HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-3+31G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138753541 | ||||||
| chr5:138753598
|
G | A | 1 | a0001c0002t0003g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-3+88G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138753598 | ||||||
| chr5:138753610
|
C | T | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-3+100C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138753610 | ||||||
| chr5:138753726
|
G | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+216G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138753726 | ||||||
| chr5:138754014
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-3+504A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138754014 | ||||||
| chr5:138754059
|
A | C | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-3+549A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138754059 | ||||||
| chr5:138754231
|
G | GT | 95 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-3+736dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138754231 | |||||
| chr5:138754241
|
T | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3+731T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138754241 | ||||||
| chr5:138754821
|
G | T | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-3+1311G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138754821 | ||||||
| chr5:138754880
|
C | T | 1 | a0001c0002t0002g0085 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-3+1370C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138754880 | ||||||
| chr5:138755002
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-3+1492C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138755002 | ||||||
| chr5:138755040
|
G | A | 1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-3+1530G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138755040 | ||||||
| chr5:138755141
|
G | GGT | 7 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+1634_-3+1635dup others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755141 | |||||
| chr5:138755332
|
G | A | 7 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(4): Show | 7 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+1822G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138755332 | ||||||
| chr5:138755845
|
C | CT | 11 | a0001c0002t0002g0003a0001c0002t0002g0078a0001c0002t0002g0079others(8): Show | 11 | HG00735.hp1 HG01070.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3+2370dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | |||||
| chr5:138755845
|
CTTTT | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0017others(4): Show | 7 | HG02074.hp2 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+2367_-3+2370del others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | |||||
| chr5:138755845
|
CTTTTT | C | 14 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(11): Show | 14 | HG00438.hp2 HG01243.hp1 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3+2366_-3+2370del others(5): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | |||||
| chr5:138755845
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0179 | 3 | HG01361.hp1 HG02129.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.-3+2361_-3+2370del others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | |||||
| chr5:138755845
|
CTTTTTTT others(4): Show |
C | 75 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.-3+2360_-3+2370del others(11): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | |||||
| chr5:138755845
|
CTTTTTTT others(5): Show |
C | 16 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0091others(13): Show | 16 | HG01243.hp2 HG01516.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-3+2359_-3+2370del others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | |||||
| chr5:138755845
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | NA18946.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.-3+2358_-3+2370del others(13): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | |||||
| chr5:138755845
|
CTTTTTTT others(8): Show |
C | 6 | a0001c0002t0003g0033a0001c0002t0003g0034a0001c0004t0004g0005others(3): Show | 6 | HG00741.hp1 HG02486.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3+2356_-3+2370del others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | |||||
| chr5:138755845
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0002t0003g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-3+2355_-3+2370del others(16): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | |||||
| chr5:138755845
|
CTTTTTTT others(12): Show |
C | 12 | a0001c0001t0006g0174a0001c0001t0006g0175a0001c0002t0003g0021others(9): Show | 12 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+2352_-3+2370del others(19): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | |||||
| chr5:138755845
|
CTTTTTTT others(13): Show |
C | 2 | a0001c0002t0003g0020a0001c0002t0003g0027 | 2 | HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-3+2351_-3+2370del others(20): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | |||||
| chr5:138755845
|
CTTTTTTT others(15): Show |
C | 1 | a0001c0002t0005g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-3+2349_-3+2370del others(22): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | |||||
| chr5:138755934
|
C | T | 2 | a0001c0001t0001g0087a0004c0010t0001g0169 | 2 | HG00423.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-3+2424C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138755934 | ||||||
| chr5:138756008
|
T | G | 7 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(4): Show | 7 | HG00423.hp1 HG02132.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+2498T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138756008 | ||||||
| chr5:138756027
|
C | CTTAT | 2 | a0001c0002t0003g0029a0001c0002t0008g0028 | 2 | HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-3+2544_-3+2547dup others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138756027 | |||||
| chr5:138756027
|
CTTAT | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(110): Show | 113 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.-3+2544_-3+2547del others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138756027 | |||||
| chr5:138756382
|
G | C | 2 | a0001c0001t0006g0174a0001c0001t0006g0175 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-3+2872G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138756382 | ||||||
| chr5:138756607
|
G | T | 2 | a0001c0005t0001g0167a0001c0005t0001g0168 | 2 | HG00099.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-3+3097G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138756607 | ||||||
| chr5:138756783
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-3+3273G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138756783 | ||||||
| chr5:138756795
|
G | A | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+3285G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138756795 | ||||||
| chr5:138756978
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-3+3468C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138756978 | ||||||
| chr5:138757028
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-3+3518G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138757028 | ||||||
| chr5:138757194
|
TCAAA | T | 2 | a0001c0001t0007g0111a0001c0001t0007g0112 | 2 | HG01099.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.-3+3689_-3+3692del others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138757194 | |||||
| chr5:138757327
|
A | G | 3 | a0001c0002t0002g0074a0001c0002t0002g0075a0001c0002t0002g0084 | 3 | HG01070.hp2 HG01071.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.-3+3817A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138757327 | ||||||
| chr5:138757420
|
G | C | 12 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(9): Show | 12 | HG00423.hp2 HG01243.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+3910G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138757420 | ||||||
| chr5:138757494
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-3+3984T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138757494 | ||||||
| chr5:138757625
|
G | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3+4115G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138757625 | ||||||
| chr5:138757732
|
AGTTCTTG others(5): Show |
A | 14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3+4225_-3+4236del others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138757732 | |||||
| chr5:138757837
|
A | G | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-3+4327A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138757837 | ||||||
| chr5:138757969
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-3+4459C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138757969 | ||||||
| chr5:138758294
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3+4784C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138758294 | ||||||
| chr5:138758318
|
C | T | 1 | a0001c0002t0002g0002 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-3+4808C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138758318 | ||||||
| chr5:138758347
|
G | A | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-3+4837G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138758347 | ||||||
| chr5:138758524
|
A | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3+5014A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138758524 | ||||||
| chr5:138758534
|
G | A | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+5024G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138758534 | ||||||
| chr5:138758749
|
A | G | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-3+5239A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138758749 | ||||||
| chr5:138758960
|
C | T | 4 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+5450C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138758960 | ||||||
| chr5:138759147
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-3+5637G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138759147 | ||||||
| chr5:138759516
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-3+6006C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138759516 | ||||||
| chr5:138759517
|
A | G | 95 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-3+6007A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138759517 | ||||||
| chr5:138759863
|
T | A | 2 | a0001c0003t0002g0076a0001c0003t0002g0077 | 2 | HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-3+6353T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138759863 | ||||||
| chr5:138759923
|
T | G | 1 | a0001c0002t0008g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-3+6413T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138759923 | ||||||
| chr5:138759954
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-3+6444T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138759954 | ||||||
| chr5:138759980
|
C | CT | 14 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0098others(11): Show | 14 | HG00323.hp1 HG00735.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.-3+6499dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138759980 | |||||
| chr5:138759980
|
CT | C | 69 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(66): Show | 69 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.-3+6499delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138759980 | |||||
| chr5:138759980
|
CTT | C | 25 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(22): Show | 25 | HG00423.hp1 HG00438.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.-3+6498_-3+6499del others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138759980 | |||||
| chr5:138759980
|
CTTT | C | 8 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0002t0003g0021others(5): Show | 8 | HG01099.hp2 HG01109.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+6497_-3+6499del others(3): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138759980 | |||||
| chr5:138760241
|
G | A | 1 | a0001c0004t0004g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-3+6731G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138760241 | ||||||
| chr5:138760371
|
C | CT | 111 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.-3+6871dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138760371 | |||||
| chr5:138760413
|
G | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3+6903G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138760413 | ||||||
| chr5:138760417
|
G | A | 14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3+6907G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138760417 | ||||||
| chr5:138760462
|
CA | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-3+6956delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138760462 | |||||
| chr5:138760624
|
G | A | 2 | a0003c0007t0001g0099a0003c0007t0001g0100 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-3+7114G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138760624 | ||||||
| chr5:138760658
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-3+7148G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138760658 | ||||||
| chr5:138760894
|
G | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0166a0001c0001t0001g0170 | 3 | HG00323.hp2 HG02129.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-3+7384G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138760894 | ||||||
| chr5:138761127
|
A | G | 3 | a0001c0001t0001g0153a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | HG01074.hp2 HG01081.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-3+7617A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138761127 | ||||||
| chr5:138761273
|
C | T | 2 | a0001c0001t0001g0087a0004c0010t0001g0169 | 2 | HG00423.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-3+7763C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138761273 | ||||||
| chr5:138761315
|
A | G | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+7805A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138761315 | ||||||
| chr5:138761322
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3+7812C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138761322 | ||||||
| chr5:138761479
|
C | A | 14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3+7969C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138761479 | ||||||
| chr5:138761480
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-3+7970G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138761480 | ||||||
| chr5:138761486
|
C | T | 9 | a0001c0001t0001g0103a0001c0001t0001g0151a0001c0001t0001g0152others(6): Show | 9 | HG00639.hp2 HG01070.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3+7976C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138761486 | ||||||
| chr5:138761595
|
T | C | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+8085T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138761595 | ||||||
| chr5:138761603
|
T | TA | 114 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-3+8100dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138761603 | |||||
| chr5:138762035
|
C | T | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-3+8525C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138762035 | ||||||
| chr5:138762093
|
A | G | 2 | a0001c0002t0002g0075a0001c0002t0002g0084 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-3+8583A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138762093 | ||||||
| chr5:138762247
|
C | T | 95 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-3+8737C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138762247 | ||||||
| chr5:138762375
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-3+8865C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138762375 | ||||||
| chr5:138762487
|
G | GT | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-3+8986dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138762487 | |||||
| chr5:138762733
|
C | T | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+9223C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138762733 | ||||||
| chr5:138762741
|
C | T | 95 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-3+9231C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138762741 | ||||||
| chr5:138762789
|
CTG | C | 95 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-3+9281_-3+9282del others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138762789 | |||||
| chr5:138762827
|
G | T | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-3+9317G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138762827 | ||||||
| chr5:138762862
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-3+9352T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138762862 | ||||||
| chr5:138762993
|
A | G | 83 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-3+9483A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138762993 | ||||||
| chr5:138763083
|
A | G | 1 | a0001c0009t0004g0006 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-3+9573A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138763083 | ||||||
| chr5:138763099
|
G | GT | 109 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.-3+9598dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138763099 | |||||
| chr5:138763332
|
C | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-3+9822C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138763332 | ||||||
| chr5:138763408
|
A | G | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+9898A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138763408 | ||||||
| chr5:138763496
|
C | T | 12 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(9): Show | 12 | HG00423.hp2 HG01243.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+9986C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138763496 | ||||||
| chr5:138763583
|
A | G | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-3+10073A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138763583 | ||||||
| chr5:138763727
|
G | C | 1 | a0001c0002t0002g0067 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-3+10217G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138763727 | ||||||
| chr5:138763816
|
TGTC | T | 3 | a0001c0002t0005g0026a0001c0002t0005g0050a0001c0002t0005g0068 | 3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-3+10307_-3+10309d others(5): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138763816 | ||||||
| chr5:138763882
|
AGT | A | 83 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-3+10377_-3+10378d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138763882 | |||||
| chr5:138763908
|
A | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-3+10398A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138763908 | ||||||
| chr5:138764145
|
A | G | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+10635A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764145 | ||||||
| chr5:138764171
|
C | T | 2 | a0001c0002t0002g0066a0001c0002t0002g0083 | 2 | HG00639.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.-3+10661C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764171 | ||||||
| chr5:138764185
|
AAAAAAAC | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+10696_-3+10702d others(9): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138764185 | |||||
| chr5:138764304
|
T | C | 3 | a0001c0002t0003g0032a0001c0002t0003g0033a0001c0002t0003g0034 | 3 | HG00741.hp1 HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-3+10794T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764304 | ||||||
| chr5:138764320
|
C | T | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+10810C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764320 | ||||||
| chr5:138764353
|
T | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-3+10843T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764353 | ||||||
| chr5:138764483
|
T | A | 1 | a0001c0002t0003g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-3+10973T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764483 | ||||||
| chr5:138764623
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-3+11113C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764623 | ||||||
| chr5:138764766
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-3+11256T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764766 | ||||||
| chr5:138764776
|
A | G | 3 | a0001c0002t0003g0029a0001c0002t0008g0028a0001c0013t0003g0031 | 3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-3+11266A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764776 | ||||||
| chr5:138764868
|
C | CT | 30 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0091others(27): Show | 30 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.-3+11380dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138764868 | |||||
| chr5:138764868
|
C | CTT | 65 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.-3+11379_-3+11380d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138764868 | |||||
| chr5:138764868
|
C | CTTT | 25 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0088others(22): Show | 25 | HG00423.hp1 HG00735.hp2 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.-3+11378_-3+11380d others(5): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138764868 | |||||
| chr5:138764868
|
CT | C | 16 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(13): Show | 16 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-3+11380delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138764868 | |||||
| chr5:138764869
|
T | TC | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+11359_-3+11360i others(3): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764869 | ||||||
| chr5:138764906
|
C | T | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-3+11396C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764906 | ||||||
| chr5:138765186
|
AC | A | 10 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0051others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3+11679delC | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138765186 | |||||
| chr5:138765197
|
C | T | 1 | a0001c0002t0002g0002 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-3+11687C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138765197 | ||||||
| chr5:138765309
|
A | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-3+11799A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138765309 | ||||||
| chr5:138765331
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02698.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-3+11821G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138765331 | ||||||
| chr5:138765333
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(12): Show | 15 | HG01099.hp2 HG02257.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+11823G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138765333 | ||||||
| chr5:138765348
|
A | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-3+11838A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138765348 | ||||||
| chr5:138765409
|
T | C | 11 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0117others(8): Show | 11 | HG00099.hp2 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.-3+11899T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138765409 | ||||||
| chr5:138765779
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-3+12269T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138765779 | ||||||
| chr5:138765839
|
C | G | 4 | a0001c0001t0001g0113a0001c0001t0001g0119a0001c0001t0001g0120others(1): Show | 4 | HG01433.hp1 HG01975.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+12329C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138765839 | ||||||
| chr5:138765897
|
C | T | 32 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(29): Show | 32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.-3+12387C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138765897 | ||||||
| chr5:138765947
|
C | CA | 17 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(14): Show | 17 | HG00423.hp1 HG00642.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.-3+12461dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138765947 | |||||
| chr5:138765947
|
CA | C | 37 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0040others(34): Show | 37 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.-3+12461delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138765947 | |||||
| chr5:138765947
|
CAA | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(4): Show | 7 | HG00423.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+12460_-3+12461d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138765947 | |||||
| chr5:138765971
|
A | G | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-3+12461A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138765971 | ||||||
| chr5:138766137
|
C | CACAT | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+12631_-3+12634d others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138766137 | |||||
| chr5:138766229
|
C | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-3+12719C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138766229 | ||||||
| chr5:138766451
|
G | GT | 105 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-3+12956dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138766451 | |||||
| chr5:138766451
|
G | T | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG02451.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+12941G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138766451 | ||||||
| chr5:138766456
|
T | G | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-3+12946T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138766456 | ||||||
| chr5:138766489
|
A | G | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+12979A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138766489 | ||||||
| chr5:138766761
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-3+13251A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138766761 | ||||||
| chr5:138766800
|
T | G | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+13290T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138766800 | ||||||
| chr5:138766861
|
G | A | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-3+13351G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138766861 | ||||||
| chr5:138766974
|
A | G | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-3+13464A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138766974 | ||||||
| chr5:138767031
|
A | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.-3+13521A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138767031 | ||||||
| chr5:138767033
|
T | TTTTC | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-3+13535_-3+13538d others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138767033 | |||||
| chr5:138767053
|
T | G | 1 | a0001c0001t0001g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-3+13543T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138767053 | ||||||
| chr5:138767071
|
C | G | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-3+13561C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138767071 | ||||||
| chr5:138767283
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.-3+13773A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138767283 | ||||||
| chr5:138767577
|
A | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-3+14067A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138767577 | ||||||
| chr5:138767647
|
T | G | 1 | a0001c0001t0001g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-3+14137T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138767647 | ||||||
| chr5:138767949
|
A | C | 4 | a0001c0002t0005g0026a0001c0002t0005g0050a0001c0002t0005g0068others(1): Show | 4 | HG02647.hp1 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-13974A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138767949 | ||||||
| chr5:138768198
|
A | G | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-2-13725A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138768198 | ||||||
| chr5:138768322
|
C | G | 2 | a0001c0002t0002g0070a0001c0002t0002g0079 | 2 | HG03942.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-2-13601C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138768322 | ||||||
| chr5:138768338
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-2-13585C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138768338 | ||||||
| chr5:138768558
|
G | GT | 8 | a0001c0001t0001g0018a0001c0001t0006g0174a0001c0001t0006g0175others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-13341dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138768558 | |||||
| chr5:138768558
|
G | GTT | 8 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-13342_-2-13341d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138768558 | |||||
| chr5:138768558
|
GT | G | 79 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0086others(76): Show | 79 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.-2-13341delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138768558 | |||||
| chr5:138768558
|
GTT | G | 26 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(23): Show | 26 | HG00323.hp2 HG00438.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.-2-13342_-2-13341d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138768558 | |||||
| chr5:138768568
|
T | G | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2-13355T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138768568 | ||||||
| chr5:138768654
|
A | C | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2-13269A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138768654 | ||||||
| chr5:138768924
|
C | T | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2-12999C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138768924 | ||||||
| chr5:138769009
|
A | G | 4 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-12914A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138769009 | ||||||
| chr5:138769081
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-2-12842T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138769081 | ||||||
| chr5:138769144
|
T | A | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-2-12779T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138769144 | ||||||
| chr5:138769210
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-2-12713C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138769210 | ||||||
| chr5:138769336
|
C | G | 1 | a0001c0002t0003g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-2-12587C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138769336 | ||||||
| chr5:138769379
|
G | GTTA | 6 | a0001c0002t0002g0057a0001c0002t0002g0058a0001c0002t0002g0066others(3): Show | 6 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-12523_-2-12521d others(5): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138769379 | |||||
| chr5:138769667
|
C | T | 14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2-12256C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138769667 | ||||||
| chr5:138769787
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-2-12136C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138769787 | ||||||
| chr5:138769794
|
A | C | 4 | a0001c0001t0001g0088a0001c0001t0001g0149a0003c0007t0001g0099others(1): Show | 4 | HG02723.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-12129A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138769794 | ||||||
| chr5:138769826
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-2-12097C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138769826 | ||||||
| chr5:138769915
|
C | T | 1 | a0001c0002t0002g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-2-12008C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138769915 | ||||||
| chr5:138770124
|
C | T | 1 | a0001c0002t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-2-11799C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138770124 | ||||||
| chr5:138770145
|
T | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-11778T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138770145 | ||||||
| chr5:138770269
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp2 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-11654G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138770269 | ||||||
| chr5:138770637
|
T | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-2-11286T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138770637 | ||||||
| chr5:138770641
|
C | T | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-11282C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138770641 | ||||||
| chr5:138770671
|
C | T | 3 | a0001c0002t0002g0051a0001c0002t0002g0071a0001c0002t0002g0078 | 3 | HG01081.hp2 HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-2-11252C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138770671 | ||||||
| chr5:138770695
|
T | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-2-11228T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138770695 | ||||||
| chr5:138770747
|
G | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-2-11176G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138770747 | ||||||
| chr5:138770808
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-2-11115C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138770808 | ||||||
| chr5:138770896
|
G | A | 2 | a0001c0002t0003g0029a0001c0002t0008g0028 | 2 | HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2-11027G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138770896 | ||||||
| chr5:138770950
|
CA | C | 86 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-2-10958delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138770950 | |||||
| chr5:138771153
|
A | G | 1 | a0001c0002t0005g0050 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-2-10770A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138771153 | ||||||
| chr5:138771172
|
C | T | 10 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(7): Show | 10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-10751C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138771172 | ||||||
| chr5:138771210
|
A | AT | 5 | a0001c0002t0002g0002a0001c0004t0004g0005a0001c0004t0004g0007others(2): Show | 5 | HG01981.hp1 HG02486.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-10701dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138771210 | |||||
| chr5:138771301
|
C | G | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-2-10622C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138771301 | ||||||
| chr5:138771740
|
A | C | 1 | a0001c0002t0003g0044 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-2-10183A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138771740 | ||||||
| chr5:138771762
|
A | T | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-2-10161A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138771762 | ||||||
| chr5:138771865
|
A | G | 1 | a0001c0002t0003g0048 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-2-10058A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138771865 | ||||||
| chr5:138771926
|
T | TA | 19 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp2 HG01993.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-2-9987dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138771926 | |||||
| chr5:138771948
|
T | G | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2-9975T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138771948 | ||||||
| chr5:138772035
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-2-9888T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138772035 | ||||||
| chr5:138772203
|
A | G | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-2-9720A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138772203 | ||||||
| chr5:138772237
|
T | C | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2-9686T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138772237 | ||||||
| chr5:138772789
|
GGGATTTG others(68): Show |
G | 179 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-2-9017_-2-8943del others(75): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138772789 | |||||
| chr5:138773014
|
T | C | 10 | a0001c0001t0001g0088a0001c0001t0001g0102a0001c0001t0001g0114others(7): Show | 10 | HG02132.hp1 HG02602.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2-8909T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138773014 | ||||||
| chr5:138773254
|
G | A | 1 | a0001c0002t0003g0021 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-2-8669G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138773254 | ||||||
| chr5:138773261
|
C | T | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-8662C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138773261 | ||||||
| chr5:138773335
|
C | T | 5 | a0001c0001t0001g0106a0001c0004t0004g0005a0001c0004t0004g0007others(2): Show | 5 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-8588C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138773335 | ||||||
| chr5:138773559
|
T | C | 3 | a0001c0002t0003g0020a0001c0002t0003g0025a0001c0012t0003g0019 | 3 | HG02280.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-2-8364T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138773559 | ||||||
| chr5:138773652
|
T | TAG | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-2-8268_-2-8267dup others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138773652 | |||||
| chr5:138773680
|
AG | A | 10 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(7): Show | 10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-8242delG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138773680 | ||||||
| chr5:138773696
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-8227C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138773696 | ||||||
| chr5:138773850
|
A | G | 1 | a0001c0002t0003g0024 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-2-8073A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138773850 | ||||||
| chr5:138774151
|
G | A | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-2-7772G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138774151 | ||||||
| chr5:138774383
|
T | G | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-2-7540T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138774383 | ||||||
| chr5:138774402
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-2-7521T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138774402 | ||||||
| chr5:138774484
|
C | G | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-2-7439C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138774484 | ||||||
| chr5:138774832
|
A | ATC | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-2-7088_-2-7087dup others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138774832 | |||||
| chr5:138774851
|
C | T | 95 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-2-7072C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138774851 | ||||||
| chr5:138774905
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-2-7018G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138774905 | ||||||
| chr5:138775013
|
A | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-2-6910A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138775013 | ||||||
| chr5:138775209
|
A | T | 3 | a0001c0002t0003g0029a0001c0002t0008g0028a0001c0013t0003g0031 | 3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2-6714A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138775209 | ||||||
| chr5:138775261
|
A | G | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-2-6662A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138775261 | ||||||
| chr5:138775430
|
A | G | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-2-6493A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138775430 | ||||||
| chr5:138775502
|
C | T | 3 | a0001c0002t0002g0051a0001c0002t0002g0071a0001c0002t0002g0078 | 3 | HG01081.hp2 HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-2-6421C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138775502 | ||||||
| chr5:138775714
|
C | CT | 45 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0088others(42): Show | 45 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.-2-6184dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138775714 | |||||
| chr5:138775714
|
CT | C | 28 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(25): Show | 28 | HG00423.hp2 HG00438.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-2-6184delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138775714 | |||||
| chr5:138775714
|
CTTTTTTT others(1): Show |
C | 10 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(7): Show | 10 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2-6191_-2-6184del others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138775714 | |||||
| chr5:138775762
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-2-6161G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138775762 | ||||||
| chr5:138775773
|
A | C | 1 | a0001c0002t0003g0047 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-2-6150A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138775773 | ||||||
| chr5:138775803
|
A | G | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2-6120A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138775803 | ||||||
| chr5:138775917
|
G | A | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-2-6006G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138775917 | ||||||
| chr5:138775963
|
T | C | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-2-5960T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138775963 | ||||||
| chr5:138776037
|
T | G | 1 | a0001c0001t0001g0011 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-2-5886T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776037 | ||||||
| chr5:138776039
|
C | CT | 90 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.-2-5860dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138776039 | |||||
| chr5:138776039
|
C | CTT | 29 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(26): Show | 29 | HG00438.hp1 HG00642.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-2-5861_-2-5860dup others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138776039 | |||||
| chr5:138776039
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-2-5884C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776039 | ||||||
| chr5:138776039
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0003t0002g0055 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-2-5872_-2-5860del others(13): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138776039 | |||||
| chr5:138776159
|
GTCTCTGG others(182): Show |
G | 4 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0045others(1): Show | 4 | HG00438.hp2 HG02074.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-5763_-2-5575del | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776159 | ||||||
| chr5:138776330
|
C | G | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-2-5593C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776330 | ||||||
| chr5:138776349
|
C | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0045others(1): Show | 4 | HG00438.hp2 HG02074.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-5574C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776349 | ||||||
| chr5:138776350
|
A | G | 4 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0045others(1): Show | 4 | HG00438.hp2 HG02074.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-5573A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776350 | ||||||
| chr5:138776379
|
G | A | 1 | a0002c0006t0001g0090 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-2-5544G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776379 | ||||||
| chr5:138776458
|
C | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0088a0001c0001t0001g0149others(2): Show | 5 | HG02723.hp2 HG02965.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-5465C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776458 | ||||||
| chr5:138776475
|
A | C | 1 | a0001c0001t0001g0108 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-2-5448A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776475 | ||||||
| chr5:138776586
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-2-5337G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776586 | ||||||
| chr5:138776632
|
C | T | 1 | a0001c0002t0005g0068 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-2-5291C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776632 | ||||||
| chr5:138776657
|
G | T | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-2-5266G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776657 | ||||||
| chr5:138776679
|
C | A | 2 | a0001c0002t0003g0029a0001c0002t0008g0028 | 2 | HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2-5244C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776679 | ||||||
| chr5:138776804
|
A | AC | 14 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(11): Show | 14 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2-5112dupC | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138776804 | |||||
| chr5:138776826
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-2-5097C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776826 | ||||||
| chr5:138776843
|
CG | C | 125 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.-2-5073delG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138776843 | |||||
| chr5:138776856
|
T | TCCCCCAC others(42): Show |
1 | a0001c0002t0002g0072 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-2-5048_-2-5000dup others(49): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138776856 | |||||
| chr5:138776867
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-5056C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776867 | ||||||
| chr5:138776875
|
GCGGGGCG others(42): Show |
G | 1 | a0001c0002t0002g0081 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-2-5029_-2-4981del others(49): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138776875 | |||||
| chr5:138776894
|
A | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-2-5029A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776894 | ||||||
| chr5:138776905
|
CCCCCCAC others(42): Show |
C | 3 | a0001c0002t0005g0026a0001c0002t0005g0050a0001c0002t0005g0068 | 3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-2-4984_-2-4936del others(49): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138776905 | |||||
| chr5:138776924
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0164 | 2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.-2-4999A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776924 | ||||||
| chr5:138776931
|
G | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-4992G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776931 | ||||||
| chr5:138776938
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-2-4985C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776938 | ||||||
| chr5:138776975
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-2-4948G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776975 | ||||||
| chr5:138776978
|
G | T | 1 | a0001c0002t0002g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-2-4945G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776978 | ||||||
| chr5:138776979
|
C | T | 1 | a0001c0002t0002g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-2-4944C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776979 | ||||||
| chr5:138776996
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-2-4927G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776996 | ||||||
| chr5:138777077
|
C | T | 1 | a0001c0002t0003g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-2-4846C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777077 | ||||||
| chr5:138777141
|
C | T | 1 | a0001c0003t0002g0055 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-2-4782C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777141 | ||||||
| chr5:138777178
|
C | CG | 4 | a0001c0001t0001g0013a0001c0001t0001g0117a0001c0002t0002g0082others(1): Show | 4 | HG01109.hp2 HG02602.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-4741dupG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777178 | |||||
| chr5:138777181
|
G | A | 12 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(9): Show | 12 | HG00423.hp2 HG01243.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-4742G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777181 | ||||||
| chr5:138777194
|
T | C | 3 | a0001c0002t0003g0029a0001c0002t0008g0028a0001c0013t0003g0031 | 3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2-4729T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777194 | ||||||
| chr5:138777201
|
G | C | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-4722G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777201 | ||||||
| chr5:138777215
|
A | G | 14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2-4708A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777215 | ||||||
| chr5:138777260
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-2-4663G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777260 | ||||||
| chr5:138777277
|
G | A | 2 | a0001c0002t0003g0029a0001c0002t0008g0028 | 2 | HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2-4646G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777277 | ||||||
| chr5:138777303
|
G | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-4620G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777303 | ||||||
| chr5:138777342
|
C | T | 5 | a0001c0002t0003g0004a0001c0002t0003g0043a0001c0002t0003g0044others(2): Show | 5 | HG01243.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-4581C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777342 | ||||||
| chr5:138777450
|
C | CG | 14 | a0001c0001t0001g0013a0001c0001t0001g0097a0001c0001t0001g0120others(11): Show | 14 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2-4469dupG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777450 | |||||
| chr5:138777506
|
C | T | 10 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(7): Show | 10 | HG00423.hp2 NA18946.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-4417C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777506 | ||||||
| chr5:138777530
|
G | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-2-4393G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777530 | ||||||
| chr5:138777552
|
C | T | 14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2-4371C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777552 | ||||||
| chr5:138777577
|
T | C | 3 | a0001c0002t0003g0029a0001c0002t0008g0028a0001c0013t0003g0031 | 3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2-4346T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777577 | ||||||
| chr5:138777665
|
G | A | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2-4258G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777665 | ||||||
| chr5:138777719
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-2-4204A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777719 | ||||||
| chr5:138777876
|
A | AGAGGGAG others(8): Show |
1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-2-4020_-2-4006dup others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777876 | |||||
| chr5:138777876
|
AGAGGGAG others(8): Show |
A | 7 | a0001c0001t0001g0166a0001c0001t0001g0170a0001c0002t0002g0071others(4): Show | 7 | HG00741.hp2 HG02129.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-4020_-2-4006del others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777876 | |||||
| chr5:138777888
|
A | AGAGGAGG others(8): Show |
4 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0001g0103others(1): Show | 4 | HG01243.hp2 HG01516.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-4021_-2-4020ins others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777888 | |||||
| chr5:138777888
|
A | AGAGGAGG others(83): Show |
1 | a0001c0001t0006g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-2-4021_-2-4020ins others(90): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777888 | |||||
| chr5:138777888
|
A | AGAGGAGG others(98): Show |
1 | a0001c0001t0006g0174 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-2-4021_-2-4020ins others(105): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777888 | |||||
| chr5:138777903
|
A | AGAGGAGG others(8): Show |
14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 14 | HG00438.hp2 HG01884.hp1 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2-3970_-2-3956dup others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777903 | |||||
| chr5:138777903
|
A | AGAGGAGG others(23): Show |
5 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0002t0003g0032others(2): Show | 5 | HG00741.hp1 HG01243.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-3985_-2-3956dup others(30): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777903 | |||||
| chr5:138777903
|
A | AGAGGAGG others(38): Show |
2 | a0001c0002t0003g0034a0001c0002t0005g0050 | 2 | HG02895.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-2-4000_-2-3956dup others(45): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777903 | |||||
| chr5:138777903
|
A | AGAGGAGG others(83): Show |
1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-2-3956_-2-3955ins others(90): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777903 | |||||
| chr5:138777903
|
A | G | 102 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.-2-4020A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777903 | ||||||
| chr5:138777913
|
GA | G | 4 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-4009delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777913 | ||||||
| chr5:138777929
|
A | AGGGGGAG others(24): Show |
1 | a0001c0002t0003g0048 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-2-3989_-2-3959dup others(31): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777929 | |||||
| chr5:138777937
|
G | GAGGGAGA others(23): Show |
12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-3957_-2-3956ins others(30): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777937 | |||||
| chr5:138777988
|
C | CT | 8 | a0001c0002t0002g0054a0001c0002t0002g0070a0001c0002t0002g0075others(5): Show | 8 | HG01071.hp1 HG01361.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-3912dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777988 | |||||
| chr5:138777988
|
C | CTT | 9 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(6): Show | 9 | HG02622.hp1 HG02970.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-3913_-2-3912dup others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777988 | |||||
| chr5:138777988
|
C | CTTT | 6 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG01099.hp2 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-3914_-2-3912dup others(3): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777988 | |||||
| chr5:138777988
|
C | CTTTT | 56 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.-2-3915_-2-3912dup others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777988 | |||||
| chr5:138777988
|
C | CTTTTT | 36 | a0001c0001t0001g0039a0001c0001t0001g0086a0001c0001t0001g0097others(33): Show | 36 | HG00423.hp2 HG00438.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.-2-3916_-2-3912dup others(5): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777988 | |||||
| chr5:138777988
|
CT | C | 15 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(12): Show | 15 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.-2-3912delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777988 | |||||
| chr5:138777988
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-2-3922_-2-3912del others(11): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777988 | |||||
| chr5:138778155
|
G | A | 4 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-3768G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138778155 | ||||||
| chr5:138778160
|
A | AT | 95 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-2-3757dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138778160 | |||||
| chr5:138778344
|
G | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-3579G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138778344 | ||||||
| chr5:138778400
|
A | G | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0165 | 3 | HG02970.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-2-3523A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138778400 | ||||||
| chr5:138778544
|
C | T | 5 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 5 | HG01070.hp1 HG01109.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-3379C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138778544 | ||||||
| chr5:138778868
|
G | T | 5 | a0001c0002t0003g0004a0001c0002t0003g0043a0001c0002t0003g0044others(2): Show | 5 | HG01243.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-3055G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138778868 | ||||||
| chr5:138778886
|
G | GT | 15 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(12): Show | 15 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2-3027dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138778886 | |||||
| chr5:138778947
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-2-2976C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138778947 | ||||||
| chr5:138779032
|
C | T | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2-2891C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138779032 | ||||||
| chr5:138779530
|
T | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-2-2393T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138779530 | ||||||
| chr5:138779536
|
A | T | 3 | a0001c0002t0005g0026a0001c0002t0005g0050a0001c0002t0005g0068 | 3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-2-2387A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138779536 | ||||||
| chr5:138779666
|
G | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-2-2257G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138779666 | ||||||
| chr5:138779717
|
G | GT | 8 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(5): Show | 8 | HG01243.hp1 HG02074.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-2201dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138779717 | |||||
| chr5:138779717
|
G | GTT | 6 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0002t0003g0032others(3): Show | 6 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-2202_-2-2201dup others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138779717 | |||||
| chr5:138779717
|
G | T | 10 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(7): Show | 10 | HG01109.hp2 HG01993.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2-2206G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138779717 | ||||||
| chr5:138779721
|
TTG | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.-2-2200_-2-2199del others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138779721 | |||||
| chr5:138779722
|
TG | T | 10 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(7): Show | 10 | HG01243.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2-2200delG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138779722 | ||||||
| chr5:138779723
|
G | T | 27 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(24): Show | 27 | HG00438.hp2 HG00741.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-2-2200G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138779723 | ||||||
| chr5:138779724
|
T | G | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-2-2199T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138779724 | ||||||
| chr5:138780242
|
C | A | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-2-1681C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780242 | ||||||
| chr5:138780276
|
G | A | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-2-1647G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780276 | ||||||
| chr5:138780346
|
C | G | 83 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-2-1577C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780346 | ||||||
| chr5:138780352
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0165 | 3 | HG02970.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-2-1571G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780352 | ||||||
| chr5:138780439
|
C | T | 3 | a0001c0005t0001g0156a0001c0005t0001g0167a0001c0005t0001g0168 | 3 | HG00099.hp1 HG00741.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-2-1484C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780439 | ||||||
| chr5:138780472
|
C | T | 4 | a0001c0001t0001g0088a0001c0001t0001g0149a0003c0007t0001g0099others(1): Show | 4 | HG02723.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-1451C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780472 | ||||||
| chr5:138780520
|
T | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-1403T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780520 | ||||||
| chr5:138780641
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-1282C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780641 | ||||||
| chr5:138780674
|
G | A | 5 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0091others(2): Show | 5 | NA18946.hp1 NA18948.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-1249G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780674 | ||||||
| chr5:138780735
|
C | T | 4 | a0001c0001t0001g0113a0001c0001t0001g0119a0001c0001t0001g0120others(1): Show | 4 | HG01433.hp1 HG01975.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-1188C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780735 | ||||||
| chr5:138780810
|
C | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp2 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-1113C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780810 | ||||||
| chr5:138780948
|
CTG | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-2-973_-2-972delGT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138780948 | |||||
| chr5:138780988
|
G | T | 1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-2-935G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780988 | ||||||
| chr5:138781152
|
C | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-771C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138781152 | ||||||
| chr5:138781236
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-2-687G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138781236 | ||||||
| chr5:138781285
|
T | A | 1 | a0001c0001t0001g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-2-638T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138781285 | ||||||
| chr5:138781554
|
CA | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 137 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-2-352delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138781554 | |||||
| chr5:138782070
|
A | G | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.105+41A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 2/17 | chr5 | 138782070 | ||||||
| chr5:138782166
|
T | G | 4 | a0001c0001t0001g0113a0001c0001t0001g0119a0001c0001t0001g0120others(1): Show | 4 | HG01433.hp1 HG01975.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+137T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 2/17 | chr5 | 138782166 | ||||||
| chr5:138782188
|
G | A | 1 | a0001c0002t0003g0048 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.105+159G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 2/17 | chr5 | 138782188 | ||||||
| chr5:138782245
|
G | A | 1 | a0001c0002t0002g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.105+216G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 2/17 | chr5 | 138782245 | ||||||
| chr5:138782249
|
A | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.105+220A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 2/17 | chr5 | 138782249 | ||||||
| chr5:138782602
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp2 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+573C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 2/17 | chr5 | 138782602 | ||||||
| chr5:138782646
|
A | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.106-531A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 2/17 | chr5 | 138782646 | ||||||
| chr5:138782649
|
G | T | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.106-528G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 2/17 | chr5 | 138782649 | ||||||
| chr5:138783709
|
A | G | 2 | a0001c0001t0006g0174a0001c0001t0006g0175 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.301+337A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138783709 | ||||||
| chr5:138783711
|
A | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.301+339A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138783711 | ||||||
| chr5:138784366
|
A | T | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.301+994A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138784366 | ||||||
| chr5:138784424
|
A | C | 6 | a0001c0003t0002g0055a0001c0003t0002g0062a0001c0003t0002g0063others(3): Show | 6 | HG00642.hp1 HG01346.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.301+1052A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138784424 | ||||||
| chr5:138784665
|
C | G | 11 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0117others(8): Show | 11 | HG00099.hp2 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.301+1293C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138784665 | ||||||
| chr5:138784675
|
T | C | 1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.301+1303T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138784675 | ||||||
| chr5:138784838
|
T | C | 1 | a0001c0002t0003g0029 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.301+1466T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138784838 | ||||||
| chr5:138784909
|
G | A | 1 | a0001c0002t0002g0082 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.301+1537G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138784909 | ||||||
| chr5:138784916
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.301+1544C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138784916 | ||||||
| chr5:138785064
|
A | AT | 126 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.301+1707dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138785064 | |||||
| chr5:138785064
|
A | ATT | 13 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(10): Show | 13 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.301+1706_301+1707d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138785064 | |||||
| chr5:138785086
|
G | A | 6 | a0001c0003t0002g0055a0001c0003t0002g0062a0001c0003t0002g0063others(3): Show | 6 | HG00642.hp1 HG01346.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.301+1714G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785086 | ||||||
| chr5:138785088
|
G | A | 1 | a0001c0002t0002g0059 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.301+1716G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785088 | ||||||
| chr5:138785139
|
T | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.301+1767T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785139 | ||||||
| chr5:138785144
|
C | A | 1 | a0001c0002t0002g0054 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.301+1772C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785144 | ||||||
| chr5:138785154
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.301+1782C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785154 | ||||||
| chr5:138785162
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.301+1790C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785162 | ||||||
| chr5:138785262
|
T | C | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+1890T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785262 | ||||||
| chr5:138785330
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010 | 3 | HG02451.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.301+1958G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785330 | ||||||
| chr5:138785349
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.301+1977T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785349 | ||||||
| chr5:138785526
|
C | CA | 179 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.301+2155dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138785526 | |||||
| chr5:138785623
|
C | T | 1 | a0001c0002t0008g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.301+2251C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785623 | ||||||
| chr5:138785646
|
C | T | 95 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.301+2274C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785646 | ||||||
| chr5:138785671
|
C | G | 1 | a0001c0002t0002g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.301+2299C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785671 | ||||||
| chr5:138785717
|
C | A | 1 | a0001c0004t0004g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.301+2345C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785717 | ||||||
| chr5:138785763
|
T | C | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+2391T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785763 | ||||||
| chr5:138785841
|
G | A | 1 | a0001c0004t0004g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.301+2469G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785841 | ||||||
| chr5:138785888
|
C | T | 1 | a0001c0002t0002g0054 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.301+2516C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785888 | ||||||
| chr5:138785892
|
C | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG00438.hp2 HG02074.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.301+2520C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785892 | ||||||
| chr5:138786246
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.301+2874T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138786246 | ||||||
| chr5:138786430
|
C | T | 10 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(7): Show | 10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.301+3058C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138786430 | ||||||
| chr5:138786504
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.301+3132C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138786504 | ||||||
| chr5:138786639
|
G | C | 1 | a0001c0001t0001g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.301+3267G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138786639 | ||||||
| chr5:138786704
|
T | A | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+3332T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138786704 | ||||||
| chr5:138787440
|
T | G | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.301+4068T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138787440 | ||||||
| chr5:138787485
|
A | G | 4 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+4113A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138787485 | ||||||
| chr5:138787538
|
T | G | 4 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+4166T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138787538 | ||||||
| chr5:138787575
|
A | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.301+4203A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138787575 | ||||||
| chr5:138787664
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.301+4292A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138787664 | ||||||
| chr5:138787698
|
T | C | 4 | a0001c0002t0005g0026a0001c0002t0005g0050a0001c0002t0005g0068others(1): Show | 4 | HG02647.hp1 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+4326T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138787698 | ||||||
| chr5:138787869
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.301+4497G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138787869 | ||||||
| chr5:138787957
|
A | G | 3 | a0001c0002t0003g0020a0001c0002t0003g0025a0001c0012t0003g0019 | 3 | HG02280.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.301+4585A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138787957 | ||||||
| chr5:138787983
|
G | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.301+4611G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138787983 | ||||||
| chr5:138788013
|
T | A | 4 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+4641T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788013 | ||||||
| chr5:138788266
|
C | T | 3 | a0001c0002t0005g0026a0001c0002t0005g0050a0001c0002t0005g0068 | 3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.301+4894C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788266 | ||||||
| chr5:138788303
|
A | G | 1 | a0001c0002t0002g0065 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.301+4931A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788303 | ||||||
| chr5:138788305
|
T | G | 82 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.301+4933T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788305 | ||||||
| chr5:138788309
|
C | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.301+4937C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788309 | ||||||
| chr5:138788382
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.301+5010G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788382 | ||||||
| chr5:138788437
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.301+5065T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788437 | ||||||
| chr5:138788587
|
C | A | 1 | a0001c0002t0002g0072 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.301+5215C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788587 | ||||||
| chr5:138788620
|
G | A | 2 | a0001c0002t0002g0075a0001c0002t0002g0084 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.301+5248G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788620 | ||||||
| chr5:138788701
|
C | T | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+5329C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788701 | ||||||
| chr5:138788765
|
A | G | 7 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(4): Show | 7 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.301+5393A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788765 | ||||||
| chr5:138788787
|
T | C | 2 | a0001c0002t0003g0029a0001c0002t0008g0028 | 2 | HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.301+5415T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788787 | ||||||
| chr5:138788810
|
T | C | 9 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(6): Show | 9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.301+5438T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788810 | ||||||
| chr5:138788845
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.301+5473A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788845 | ||||||
| chr5:138788921
|
C | T | 1 | a0001c0002t0002g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.301+5549C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788921 | ||||||
| chr5:138789022
|
C | T | 2 | a0001c0001t0006g0174a0001c0001t0006g0175 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.301+5650C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789022 | ||||||
| chr5:138789050
|
G | A | 9 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(6): Show | 9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.301+5678G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789050 | ||||||
| chr5:138789183
|
GT | G | 13 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(10): Show | 13 | HG00423.hp1 HG01433.hp2 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.301+5816delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138789183 | |||||
| chr5:138789183
|
GTT | G | 9 | a0001c0002t0005g0026a0001c0002t0005g0050a0001c0002t0005g0068others(6): Show | 9 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.301+5815_301+5816d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138789183 | |||||
| chr5:138789188
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.301+5816T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789188 | ||||||
| chr5:138789188
|
TC | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.301+5826delC | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138789188 | |||||
| chr5:138789190
|
C | T | 14 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(11): Show | 14 | HG00423.hp2 HG01074.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.301+5818C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789190 | ||||||
| chr5:138789193
|
C | G | 1 | a0001c0001t0001g0124 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.301+5821C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789193 | ||||||
| chr5:138789196
|
C | G | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.301+5824C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789196 | ||||||
| chr5:138789196
|
C | T | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.301+5824C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789196 | ||||||
| chr5:138789223
|
C | T | 1 | a0002c0006t0001g0090 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.301+5851C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789223 | ||||||
| chr5:138789400
|
G | A | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.301+6028G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789400 | ||||||
| chr5:138789497
|
G | A | 1 | a0001c0002t0002g0079 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.301+6125G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789497 | ||||||
| chr5:138789735
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.301+6363C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789735 | ||||||
| chr5:138789988
|
C | T | 1 | a0001c0009t0004g0006 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.301+6616C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789988 | ||||||
| chr5:138790237
|
G | A | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+6865G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138790237 | ||||||
| chr5:138790250
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.301+6878G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138790250 | ||||||
| chr5:138791230
|
G | A | 9 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(6): Show | 9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.301+7858G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138791230 | ||||||
| chr5:138791288
|
G | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.301+7916G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138791288 | ||||||
| chr5:138791615
|
C | CA | 29 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0046others(26): Show | 29 | HG00438.hp2 HG00642.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.301+8270dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138791615 | |||||
| chr5:138791615
|
C | CAA | 15 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0001g0097others(12): Show | 15 | HG00741.hp1 HG01243.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.301+8269_301+8270d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138791615 | |||||
| chr5:138791615
|
C | CAAA | 38 | a0001c0001t0001g0038a0001c0001t0001g0087a0001c0001t0001g0098others(35): Show | 38 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.301+8268_301+8270d others(5): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138791615 | |||||
| chr5:138791615
|
C | CAAAA | 29 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0106others(26): Show | 29 | HG00438.hp1 HG00642.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.301+8267_301+8270d others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138791615 | |||||
| chr5:138791615
|
C | CAAAAA | 13 | a0001c0001t0001g0036a0001c0001t0001g0128a0001c0001t0001g0131others(10): Show | 13 | HG01071.hp2 HG01081.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.301+8266_301+8270d others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138791615 | |||||
| chr5:138791615
|
C | CAAAAAAA | 7 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG02451.hp2 HG03453.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.301+8264_301+8270d others(9): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138791615 | |||||
| chr5:138791615
|
CAAAAAAA others(4): Show |
C | 9 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(6): Show | 9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.301+8260_301+8270d others(13): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138791615 | |||||
| chr5:138791691
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.301+8319C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138791691 | ||||||
| chr5:138791787
|
C | CT | 117 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.301+8435dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138791787 | |||||
| chr5:138791787
|
C | CTT | 24 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(21): Show | 24 | HG00438.hp1 HG01109.hp2 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.301+8434_301+8435d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138791787 | |||||
| chr5:138791787
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.301+8426_301+8435d others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138791787 | |||||
| chr5:138792038
|
G | T | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+8666G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138792038 | ||||||
| chr5:138792079
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.301+8707A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138792079 | ||||||
| chr5:138792256
|
A | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0097 | 2 | HG01243.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.301+8884A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138792256 | ||||||
| chr5:138792390
|
C | T | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.301+9018C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138792390 | ||||||
| chr5:138792414
|
T | C | 1 | a0001c0002t0002g0079 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.301+9042T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138792414 | ||||||
| chr5:138792845
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.301+9473T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138792845 | ||||||
| chr5:138792856
|
C | T | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.301+9484C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138792856 | ||||||
| chr5:138792937
|
A | G | 1 | a0002c0006t0001g0095 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.301+9565A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138792937 | ||||||
| chr5:138792998
|
G | A | 3 | a0001c0005t0001g0156a0001c0005t0001g0167a0001c0005t0001g0168 | 3 | HG00099.hp1 HG00741.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.301+9626G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138792998 | ||||||
| chr5:138793012
|
A | G | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.301+9640A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138793012 | ||||||
| chr5:138793219
|
G | A | 2 | a0001c0001t0007g0111a0001c0001t0007g0112 | 2 | HG01099.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.301+9847G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138793219 | ||||||
| chr5:138793299
|
G | A | 9 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(6): Show | 9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.301+9927G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138793299 | ||||||
| chr5:138793439
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.301+10067C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138793439 | ||||||
| chr5:138793845
|
T | A | 1 | a0001c0002t0005g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.301+10473T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138793845 | ||||||
| chr5:138794012
|
A | AT | 6 | a0001c0001t0001g0088a0001c0001t0006g0174a0001c0001t0006g0175others(3): Show | 6 | HG00741.hp2 HG02723.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.301+10663dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138794012 | |||||
| chr5:138794012
|
A | ATT | 11 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(8): Show | 11 | HG01099.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.301+10662_301+1066 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138794012 | |||||
| chr5:138794012
|
AT | A | 78 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(75): Show | 78 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.301+10663delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138794012 | |||||
| chr5:138794012
|
ATT | A | 13 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(10): Show | 13 | HG01243.hp2 HG01515.hp2 HG03486.hp1 others(10): Show |
intron_variant | MODIFIER | c.301+10662_301+1066 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138794012 | |||||
| chr5:138794056
|
C | T | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.301+10684C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138794056 | ||||||
| chr5:138794336
|
A | G | 1 | a0001c0002t0002g0061 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.301+10964A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138794336 | ||||||
| chr5:138794362
|
A | C | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.301+10990A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138794362 | ||||||
| chr5:138794577
|
T | A | 1 | a0001c0001t0001g0173 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.301+11205T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138794577 | ||||||
| chr5:138794811
|
G | T | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0165 | 3 | HG02970.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.301+11439G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138794811 | ||||||
| chr5:138795138
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.301+11766G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138795138 | ||||||
| chr5:138795151
|
C | CA | 11 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0002t0002g0070others(8): Show | 11 | HG00438.hp2 HG01109.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.301+11802dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138795151 | |||||
| chr5:138795151
|
CAA | C | 7 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(4): Show | 7 | HG01099.hp2 HG02970.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.301+11801_301+1180 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138795151 | |||||
| chr5:138795151
|
CAAA | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.301+11800_301+1180 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138795151 | |||||
| chr5:138795151
|
CAAAA | C | 9 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0091others(6): Show | 9 | HG01361.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.301+11799_301+1180 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138795151 | |||||
| chr5:138795288
|
C | T | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0165 | 3 | HG02970.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.301+11916C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138795288 | ||||||
| chr5:138795442
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.301+12070C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138795442 | ||||||
| chr5:138795659
|
T | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.301+12287T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138795659 | ||||||
| chr5:138795680
|
A | G | 6 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0091others(3): Show | 6 | NA18946.hp1 NA18948.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.301+12308A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138795680 | ||||||
| chr5:138795703
|
C | T | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.301+12331C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138795703 | ||||||
| chr5:138795749
|
C | T | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.301+12377C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138795749 | ||||||
| chr5:138795923
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0045 | 2 | NA18983.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.301+12551C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138795923 | ||||||
| chr5:138796200
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.301+12828A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138796200 | ||||||
| chr5:138796332
|
G | A | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.301+12960G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138796332 | ||||||
| chr5:138796370
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.301+12998C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138796370 | ||||||
| chr5:138796388
|
CA | C | 82 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.301+13022delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138796388 | |||||
| chr5:138796468
|
C | T | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+13096C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138796468 | ||||||
| chr5:138796538
|
C | T | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.301+13166C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138796538 | ||||||
| chr5:138796558
|
A | AGT | 136 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.301+13186_301+1318 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138796558 | ||||||
| chr5:138796566
|
G | GTAT | 4 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175others(1): Show | 4 | HG01099.hp2 HG02630.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+13194_301+1319 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138796566 | ||||||
| chr5:138796566
|
G | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.301+13194G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138796566 | ||||||
| chr5:138796969
|
AT | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.302-13065delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138796969 | |||||
| chr5:138797030
|
T | C | 1 | a0001c0002t0005g0068 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.302-13008T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138797030 | ||||||
| chr5:138797238
|
T | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0148 | 3 | HG02280.hp2 HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.302-12800T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138797238 | ||||||
| chr5:138797261
|
G | A | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.302-12777G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138797261 | ||||||
| chr5:138797771
|
C | G | 1 | a0001c0002t0003g0033 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.302-12267C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138797771 | ||||||
| chr5:138797885
|
T | TA | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.302-12143dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138797885 | |||||
| chr5:138797898
|
T | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.302-12140T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138797898 | ||||||
| chr5:138797994
|
A | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.302-12044A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138797994 | ||||||
| chr5:138798180
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.302-11858A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138798180 | ||||||
| chr5:138798193
|
CAG | C | 2 | a0001c0001t0001g0087a0004c0010t0001g0169 | 2 | HG00423.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.302-11843_302-1184 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138798193 | |||||
| chr5:138798197
|
AGTATTTG others(9): Show |
A | 1 | a0001c0002t0002g0054 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.302-11839_302-1182 others(20): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138798197 | |||||
| chr5:138798218
|
A | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0138 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.302-11820A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138798218 | ||||||
| chr5:138798571
|
G | A | 1 | a0001c0002t0005g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.302-11467G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138798571 | ||||||
| chr5:138798606
|
C | T | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.302-11432C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138798606 | ||||||
| chr5:138798864
|
C | T | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.302-11174C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138798864 | ||||||
| chr5:138799026
|
T | C | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-11012T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138799026 | ||||||
| chr5:138799061
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.302-10977G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138799061 | ||||||
| chr5:138799120
|
C | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.302-10918C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138799120 | ||||||
| chr5:138799168
|
TTTG | T | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-10867_302-1086 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138799168 | |||||
| chr5:138799221
|
C | T | 5 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0091others(2): Show | 5 | NA18946.hp1 NA18948.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-10817C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138799221 | ||||||
| chr5:138799254
|
G | A | 3 | a0001c0002t0003g0020a0001c0002t0003g0025a0001c0012t0003g0019 | 3 | HG02280.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.302-10784G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138799254 | ||||||
| chr5:138799435
|
C | T | 95 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.302-10603C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138799435 | ||||||
| chr5:138799514
|
A | G | 1 | a0001c0002t0003g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.302-10524A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138799514 | ||||||
| chr5:138799625
|
A | AT | 11 | a0001c0001t0001g0131a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG01071.hp2 HG01099.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.302-10399dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138799625 | |||||
| chr5:138799625
|
AT | A | 14 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(11): Show | 14 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.302-10399delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138799625 | |||||
| chr5:138799857
|
G | GATGGATG others(9): Show |
2 | a0001c0001t0006g0174a0001c0001t0006g0175 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.302-10178_302-1017 others(20): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138799857 | |||||
| chr5:138799857
|
G | GATGT | 55 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(52): Show | 55 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.302-10148_302-1014 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138799857 | |||||
| chr5:138799857
|
G | GATGTATG others(1): Show |
85 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(82): Show | 85 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.302-10152_302-1014 others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138799857 | |||||
| chr5:138799857
|
G | GATGTATG others(5): Show |
12 | a0001c0001t0001g0103a0001c0001t0001g0126a0001c0001t0001g0130others(9): Show | 12 | HG00438.hp1 HG00639.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.302-10156_302-1014 others(16): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138799857 | |||||
| chr5:138799878
|
ATGTATGT others(9): Show |
A | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.302-10156_302-1014 others(20): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138799878 | |||||
| chr5:138799890
|
A | ATGTATGT others(3): Show |
1 | a0001c0001t0001g0091 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.302-10145_302-1014 others(14): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138799890 | |||||
| chr5:138800000
|
G | A | 2 | a0003c0007t0001g0099a0003c0007t0001g0100 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.302-10038G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800000 | ||||||
| chr5:138800094
|
G | A | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.302-9944G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800094 | ||||||
| chr5:138800156
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.302-9882A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800156 | ||||||
| chr5:138800232
|
C | A | 78 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.302-9806C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800232 | ||||||
| chr5:138800378
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.302-9660A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800378 | ||||||
| chr5:138800494
|
A | C | 1 | a0001c0002t0002g0081 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.302-9544A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800494 | ||||||
| chr5:138800497
|
A | G | 1 | a0001c0002t0002g0067 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.302-9541A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800497 | ||||||
| chr5:138800593
|
G | A | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.302-9445G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800593 | ||||||
| chr5:138800665
|
T | C | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.302-9373T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800665 | ||||||
| chr5:138800717
|
C | T | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.302-9321C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800717 | ||||||
| chr5:138800727
|
T | G | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.302-9311T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800727 | ||||||
| chr5:138800734
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.302-9304C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800734 | ||||||
| chr5:138800768
|
A | C | 1 | a0001c0001t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.302-9270A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800768 | ||||||
| chr5:138800896
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.302-9142G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800896 | ||||||
| chr5:138800930
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.302-9108C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800930 | ||||||
| chr5:138801090
|
G | A | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.302-8948G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138801090 | ||||||
| chr5:138801227
|
T | A | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.302-8811T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138801227 | ||||||
| chr5:138801248
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.302-8790C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138801248 | ||||||
| chr5:138801265
|
G | A | 10 | a0001c0001t0001g0131a0001c0001t0001g0135a0001c0001t0001g0136others(7): Show | 10 | HG01071.hp2 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.302-8773G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138801265 | ||||||
| chr5:138801981
|
T | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.302-8057T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138801981 | ||||||
| chr5:138802039
|
A | G | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-7999A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138802039 | ||||||
| chr5:138802268
|
A | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0138 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.302-7770A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138802268 | ||||||
| chr5:138802318
|
A | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.302-7720A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138802318 | ||||||
| chr5:138802759
|
G | C | 12 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(9): Show | 12 | HG00423.hp2 HG01243.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.302-7279G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138802759 | ||||||
| chr5:138802968
|
A | AT | 6 | a0001c0002t0003g0025a0001c0004t0004g0005a0001c0004t0004g0007others(3): Show | 6 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.302-7058dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138802968 | |||||
| chr5:138802968
|
AT | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.302-7058delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138802968 | |||||
| chr5:138802980
|
T | A | 3 | a0001c0002t0003g0029a0001c0002t0008g0028a0001c0013t0003g0031 | 3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.302-7058T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138802980 | ||||||
| chr5:138803158
|
A | AT | 11 | a0001c0001t0001g0094a0001c0001t0001g0116a0001c0001t0001g0166others(8): Show | 11 | HG00323.hp2 HG01109.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.302-6865dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138803158 | |||||
| chr5:138803427
|
A | G | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.302-6611A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138803427 | ||||||
| chr5:138803500
|
T | G | 4 | a0001c0001t0001g0113a0001c0001t0001g0119a0001c0001t0001g0120others(1): Show | 4 | HG01433.hp1 HG01975.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-6538T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138803500 | ||||||
| chr5:138803521
|
T | C | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-6517T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138803521 | ||||||
| chr5:138803588
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.302-6450C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138803588 | ||||||
| chr5:138803618
|
G | T | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-6420G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138803618 | ||||||
| chr5:138803989
|
G | A | 2 | a0001c0004t0004g0005a0001c0009t0004g0006 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.302-6049G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138803989 | ||||||
| chr5:138804091
|
T | G | 32 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(29): Show | 32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.302-5947T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138804091 | ||||||
| chr5:138804285
|
G | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.302-5753G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138804285 | ||||||
| chr5:138804375
|
T | TC | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.302-5663_302-5662i others(3): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138804375 | ||||||
| chr5:138804738
|
C | CTG | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.302-5299_302-5298i others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138804738 | |||||
| chr5:138805006
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.302-5032A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138805006 | ||||||
| chr5:138805011
|
G | A | 3 | a0001c0001t0001g0098a0001c0001t0001g0157a0001c0001t0001g0173 | 3 | HG00735.hp2 NA18961.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.302-5027G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138805011 | ||||||
| chr5:138805063
|
G | T | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-4975G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138805063 | ||||||
| chr5:138805065
|
G | C | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-4973G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138805065 | ||||||
| chr5:138805108
|
A | G | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.302-4930A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138805108 | ||||||
| chr5:138805196
|
C | T | 9 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(6): Show | 9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.302-4842C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138805196 | ||||||
| chr5:138805428
|
G | A | 9 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(6): Show | 9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.302-4610G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138805428 | ||||||
| chr5:138805797
|
T | C | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.302-4241T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138805797 | ||||||
| chr5:138805863
|
G | T | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.302-4175G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138805863 | ||||||
| chr5:138805900
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.302-4138G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138805900 | ||||||
| chr5:138806601
|
T | C | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.302-3437T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138806601 | ||||||
| chr5:138807008
|
CT | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(20): Show | 23 | HG01109.hp2 HG01169.hp1 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.302-3010delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138807008 | |||||
| chr5:138807168
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.302-2870G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138807168 | ||||||
| chr5:138807613
|
TTG | T | 12 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(9): Show | 12 | HG00423.hp2 HG01243.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.302-2421_302-2420d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138807613 | |||||
| chr5:138807684
|
T | C | 14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.302-2354T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138807684 | ||||||
| chr5:138807992
|
C | A | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.302-2046C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138807992 | ||||||
| chr5:138807993
|
C | A | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.302-2045C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138807993 | ||||||
| chr5:138808018
|
T | TG | 10 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(7): Show | 10 | HG00423.hp2 NA18946.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.302-2017dupG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138808018 | |||||
| chr5:138808093
|
G | T | 9 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(6): Show | 9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.302-1945G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138808093 | ||||||
| chr5:138808140
|
G | C | 2 | a0001c0002t0003g0025a0001c0012t0003g0019 | 2 | HG02280.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.302-1898G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138808140 | ||||||
| chr5:138808263
|
C | G | 10 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(7): Show | 10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.302-1775C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138808263 | ||||||
| chr5:138808685
|
G | T | 1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.302-1353G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138808685 | ||||||
| chr5:138808695
|
T | TA | 94 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.302-1331dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138808695 | |||||
| chr5:138808695
|
T | TAA | 31 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(28): Show | 31 | HG00423.hp2 HG01099.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.302-1332_302-1331d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138808695 | |||||
| chr5:138808939
|
A | C | 2 | a0001c0001t0006g0174a0001c0001t0006g0175 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.302-1099A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138808939 | ||||||
| chr5:138809119
|
A | C | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-919A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138809119 | ||||||
| chr5:138809256
|
C | T | 4 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.302-782C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138809256 | ||||||
| chr5:138809291
|
C | T | 3 | a0001c0002t0003g0029a0001c0002t0008g0028a0001c0013t0003g0031 | 3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.302-747C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138809291 | ||||||
| chr5:138809440
|
A | G | 1 | a0003c0007t0001g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.302-598A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138809440 | ||||||
| chr5:138809574
|
T | C | 10 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(7): Show | 10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.302-464T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138809574 | ||||||
| chr5:138809683
|
T | G | 8 | a0001c0001t0001g0098a0001c0001t0001g0126a0001c0001t0001g0130others(5): Show | 8 | HG00438.hp1 HG00735.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.302-355T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138809683 | ||||||
| chr5:138809742
|
C | CT | 13 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(10): Show | 13 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.302-286dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138809742 | |||||
| chr5:138809771
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.302-267C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138809771 | ||||||
| chr5:138809851
|
A | G | 2 | a0001c0002t0002g0080a0001c0002t0002g0081 | 2 | HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.302-187A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138809851 | ||||||
| chr5:138809955
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.302-83T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138809955 | ||||||
| chr5:138810215
|
A | T | 1 | a0001c0001t0001g0041 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.468+11A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138810215 | ||||||
| chr5:138810333
|
T | G | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.468+129T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138810333 | ||||||
| chr5:138810534
|
T | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.468+330T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138810534 | ||||||
| chr5:138810725
|
A | G | 95 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.468+521A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138810725 | ||||||
| chr5:138810831
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.468+627G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138810831 | ||||||
| chr5:138810901
|
C | T | 1 | a0001c0002t0003g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.468+697C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138810901 | ||||||
| chr5:138810914
|
A | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.468+710A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138810914 | ||||||
| chr5:138810941
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.468+737C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138810941 | ||||||
| chr5:138810946
|
G | A | 1 | a0001c0002t0003g0044 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.468+742G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138810946 | ||||||
| chr5:138810963
|
A | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.468+759A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138810963 | ||||||
| chr5:138811000
|
G | A | 14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.468+796G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811000 | ||||||
| chr5:138811057
|
G | A | 10 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(7): Show | 10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+853G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811057 | ||||||
| chr5:138811200
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.469-983C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811200 | ||||||
| chr5:138811237
|
T | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.469-946T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811237 | ||||||
| chr5:138811278
|
G | A | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.469-905G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811278 | ||||||
| chr5:138811314
|
C | T | 9 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(6): Show | 9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.469-869C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811314 | ||||||
| chr5:138811352
|
G | A | 83 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.469-831G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811352 | ||||||
| chr5:138811389
|
C | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.469-794C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811389 | ||||||
| chr5:138811482
|
AG | A | 179 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.469-698delG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr5 | 138811482 | |||||
| chr5:138811510
|
C | T | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.469-673C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811510 | ||||||
| chr5:138811511
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.469-672A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811511 | ||||||
| chr5:138811566
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.469-617T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811566 | ||||||
| chr5:138811627
|
T | C | 30 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(27): Show | 30 | HG00438.hp2 HG00741.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.469-556T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811627 | ||||||
| chr5:138811653
|
C | T | 1 | a0001c0002t0003g0024 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.469-530C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811653 | ||||||
| chr5:138811673
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.469-510C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811673 | ||||||
| chr5:138811674
|
T | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.469-509T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811674 | ||||||
| chr5:138811681
|
C | T | 83 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.469-502C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811681 | ||||||
| chr5:138811702
|
G | C | 1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.469-481G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811702 | ||||||
| chr5:138811737
|
G | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.469-446G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811737 | ||||||
| chr5:138811829
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.469-354A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811829 | ||||||
| chr5:138811892
|
A | G | 1 | a0001c0002t0002g0080 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.469-291A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811892 | ||||||
| chr5:138812304
|
TAC | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010 | 3 | HG02451.hp2 HG03486.hp2 HG03579.hp2 |
splice_region_variant&intron_variant | LOW | c.588+4_588+5delCA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138812304 | |||||
| chr5:138812339
|
A | G | 1 | a0001c0002t0002g0059 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.588+37A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138812339 | ||||||
| chr5:138812347
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.588+45A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138812347 | ||||||
| chr5:138812375
|
T | C | 32 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(29): Show | 32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.588+73T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138812375 | ||||||
| chr5:138812712
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.588+410C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138812712 | ||||||
| chr5:138812759
|
C | T | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.588+457C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138812759 | ||||||
| chr5:138812929
|
C | G | 3 | a0001c0001t0001g0153a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | HG01074.hp2 HG01081.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.588+627C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138812929 | ||||||
| chr5:138813044
|
C | T | 4 | a0001c0004t0004g0005a0001c0004t0004g0180a0001c0008t0003g0030others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+742C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138813044 | ||||||
| chr5:138813161
|
G | A | 2 | a0001c0002t0003g0020a0001c0002t0003g0025 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.588+859G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138813161 | ||||||
| chr5:138813316
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0017 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.588+1014C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138813316 | ||||||
| chr5:138813341
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.588+1039G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138813341 | ||||||
| chr5:138813596
|
A | G | 1 | a0001c0002t0003g0024 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.588+1294A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138813596 | ||||||
| chr5:138813650
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.588+1348A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138813650 | ||||||
| chr5:138813779
|
C | T | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+1477C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138813779 | ||||||
| chr5:138813843
|
C | T | 1 | a0003c0007t0001g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.588+1541C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138813843 | ||||||
| chr5:138814156
|
T | A | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.588+1854T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138814156 | ||||||
| chr5:138814158
|
T | A | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.588+1856T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138814158 | ||||||
| chr5:138814250
|
C | CT | 29 | a0001c0001t0001g0014a0001c0001t0001g0040a0001c0001t0001g0041others(26): Show | 29 | HG00438.hp2 HG00741.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.588+1963dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138814250 | |||||
| chr5:138814330
|
C | A | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.588+2028C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138814330 | ||||||
| chr5:138814430
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.588+2128A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138814430 | ||||||
| chr5:138814721
|
T | C | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.588+2419T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138814721 | ||||||
| chr5:138814762
|
G | GT | 14 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(11): Show | 14 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.588+2469dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138814762 | |||||
| chr5:138814763
|
T | G | 9 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(6): Show | 9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.588+2461T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138814763 | ||||||
| chr5:138814834
|
A | C | 1 | a0001c0001t0001g0041 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.588+2532A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138814834 | ||||||
| chr5:138814968
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.588+2666A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138814968 | ||||||
| chr5:138815048
|
T | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.588+2746T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138815048 | ||||||
| chr5:138815049
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.588+2747G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138815049 | ||||||
| chr5:138815179
|
A | G | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+2877A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138815179 | ||||||
| chr5:138815464
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.588+3162G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138815464 | ||||||
| chr5:138815502
|
G | C | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.588+3200G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138815502 | ||||||
| chr5:138815584
|
A | G | 1 | a0001c0002t0003g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.588+3282A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138815584 | ||||||
| chr5:138815636
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.588+3334G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138815636 | ||||||
| chr5:138815690
|
T | G | 1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.588+3388T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138815690 | ||||||
| chr5:138815992
|
T | C | 9 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(6): Show | 9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.588+3690T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138815992 | ||||||
| chr5:138816202
|
T | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.588+3900T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138816202 | ||||||
| chr5:138816696
|
G | A | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.588+4394G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138816696 | ||||||
| chr5:138816759
|
G | A | 1 | a0001c0002t0008g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.588+4457G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138816759 | ||||||
| chr5:138816769
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.588+4467C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138816769 | ||||||
| chr5:138816805
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.588+4503A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138816805 | ||||||
| chr5:138816937
|
G | A | 10 | a0001c0001t0001g0131a0001c0001t0001g0135a0001c0001t0001g0136others(7): Show | 10 | HG01071.hp2 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.588+4635G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138816937 | ||||||
| chr5:138816944
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.588+4642A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138816944 | ||||||
| chr5:138817133
|
C | G | 4 | a0001c0001t0001g0088a0001c0001t0001g0149a0003c0007t0001g0099others(1): Show | 4 | HG02723.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+4831C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138817133 | ||||||
| chr5:138817253
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02698.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.588+4951A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138817253 | ||||||
| chr5:138817263
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.588+4961T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138817263 | ||||||
| chr5:138817503
|
G | A | 9 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(6): Show | 9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.588+5201G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138817503 | ||||||
| chr5:138817655
|
A | C | 1 | a0001c0002t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.588+5353A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138817655 | ||||||
| chr5:138817731
|
C | T | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.588+5429C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138817731 | ||||||
| chr5:138817913
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.588+5611G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138817913 | ||||||
| chr5:138818057
|
T | C | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.588+5755T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138818057 | ||||||
| chr5:138818134
|
C | CT | 6 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(3): Show | 6 | HG00741.hp2 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+5845dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138818134 | |||||
| chr5:138818138
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.588+5836T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138818138 | ||||||
| chr5:138818147
|
T | C | 1 | a0001c0003t0002g0055 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.588+5845T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138818147 | ||||||
| chr5:138818267
|
CT | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.588+5979delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138818267 | |||||
| chr5:138818281
|
T | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.588+5979T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138818281 | ||||||
| chr5:138818332
|
C | T | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.588+6030C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138818332 | ||||||
| chr5:138818414
|
T | TA | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.588+6113dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138818414 | |||||
| chr5:138818597
|
G | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.589-5933G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138818597 | ||||||
| chr5:138818841
|
C | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.589-5689C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138818841 | ||||||
| chr5:138818894
|
C | T | 1 | a0001c0003t0002g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.589-5636C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138818894 | ||||||
| chr5:138818926
|
C | T | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.589-5604C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138818926 | ||||||
| chr5:138819023
|
G | C | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG02451.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-5507G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819023 | ||||||
| chr5:138819042
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.589-5488T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819042 | ||||||
| chr5:138819065
|
C | T | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.589-5465C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819065 | ||||||
| chr5:138819069
|
A | AC | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.589-5461_589-5460i others(3): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819069 | ||||||
| chr5:138819208
|
C | T | 2 | a0001c0001t0001g0170a0001c0004t0004g0180 | 2 | HG02129.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.589-5322C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819208 | ||||||
| chr5:138819213
|
G | A | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.589-5317G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819213 | ||||||
| chr5:138819333
|
C | T | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-5197C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819333 | ||||||
| chr5:138819424
|
G | A | 4 | a0001c0002t0005g0026a0001c0002t0005g0050a0001c0002t0005g0068others(1): Show | 4 | HG02647.hp1 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-5106G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819424 | ||||||
| chr5:138819556
|
G | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.589-4974G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819556 | ||||||
| chr5:138819689
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.589-4841C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819689 | ||||||
| chr5:138819719
|
C | G | 2 | a0003c0007t0001g0099a0003c0007t0001g0100 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.589-4811C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819719 | ||||||
| chr5:138819781
|
C | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.589-4749C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819781 | ||||||
| chr5:138819963
|
C | G | 1 | a0001c0011t0001g0107 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.589-4567C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819963 | ||||||
| chr5:138820236
|
A | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.589-4294A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138820236 | ||||||
| chr5:138820243
|
G | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.589-4287G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138820243 | ||||||
| chr5:138820270
|
G | C | 78 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.589-4260G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138820270 | ||||||
| chr5:138820324
|
A | G | 1 | a0001c0002t0003g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.589-4206A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138820324 | ||||||
| chr5:138820375
|
G | T | 9 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(6): Show | 9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.589-4155G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138820375 | ||||||
| chr5:138820493
|
T | C | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.589-4037T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138820493 | ||||||
| chr5:138820531
|
CT | C | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.589-3997delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138820531 | |||||
| chr5:138820748
|
A | AG | 95 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.589-3776dupG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138820748 | |||||
| chr5:138820818
|
A | G | 1 | a0001c0014t0001g0145 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.589-3712A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138820818 | ||||||
| chr5:138820867
|
G | A | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-3663G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138820867 | ||||||
| chr5:138821123
|
C | G | 1 | a0001c0002t0005g0050 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.589-3407C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138821123 | ||||||
| chr5:138822466
|
G | A | 12 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(9): Show | 12 | HG00423.hp2 HG01243.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.589-2064G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138822466 | ||||||
| chr5:138822530
|
C | T | 1 | a0001c0013t0003g0031 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.589-2000C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138822530 | ||||||
| chr5:138822657
|
A | T | 10 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(7): Show | 10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.589-1873A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138822657 | ||||||
| chr5:138823589
|
T | G | 1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.589-941T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138823589 | ||||||
| chr5:138823606
|
G | A | 1 | a0001c0002t0002g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.589-924G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138823606 | ||||||
| chr5:138823613
|
A | C | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.589-917A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138823613 | ||||||
| chr5:138823630
|
C | G | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.589-900C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138823630 | ||||||
| chr5:138823655
|
T | C | 95 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.589-875T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138823655 | ||||||
| chr5:138823728
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.589-802C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138823728 | ||||||
| chr5:138823813
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0176 | 2 | HG01099.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.589-717C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138823813 | ||||||
| chr5:138823956
|
C | CAAAAAAA others(1): Show |
7 | a0001c0002t0002g0035a0001c0002t0002g0057a0001c0002t0002g0067others(4): Show | 7 | HG00323.hp1 HG00642.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.589-551_589-544dup others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | |||||
| chr5:138823956
|
C | CAAAAAAA others(2): Show |
7 | a0001c0002t0002g0061a0001c0002t0002g0065a0001c0002t0002g0070others(4): Show | 7 | HG01361.hp2 HG02735.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.589-552_589-544dup others(9): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | |||||
| chr5:138823956
|
C | CAAAAAAA others(3): Show |
1 | a0001c0002t0002g0051 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.589-553_589-544dup others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | |||||
| chr5:138823956
|
C | CAAAAAAA others(4): Show |
4 | a0001c0002t0002g0056a0001c0002t0002g0060a0001c0002t0002g0073others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-554_589-544dup others(11): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | |||||
| chr5:138823956
|
C | CAAAAAAA others(5): Show |
6 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0066others(3): Show | 6 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-555_589-544dup others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | |||||
| chr5:138823956
|
C | CAAAAAAA others(6): Show |
1 | a0001c0002t0002g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.589-556_589-544dup others(13): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | |||||
| chr5:138823956
|
C | CAAAAAAA others(7): Show |
1 | a0001c0002t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.589-557_589-544dup others(14): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | |||||
| chr5:138823956
|
C | CAAAAAAA others(12): Show |
2 | a0001c0002t0002g0080a0001c0002t0002g0081 | 2 | HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.589-562_589-544dup others(19): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | |||||
| chr5:138823956
|
C | CAAAAAAA others(14): Show |
1 | a0001c0002t0002g0082 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.589-564_589-544dup others(21): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | |||||
| chr5:138823956
|
CAA | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(12): Show | 15 | HG01099.hp2 HG02257.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.589-545_589-544del others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | |||||
| chr5:138823956
|
CAAA | C | 12 | a0001c0001t0001g0087a0001c0001t0001g0101a0001c0001t0001g0104others(9): Show | 12 | HG00423.hp1 HG01891.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.589-546_589-544del others(3): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | |||||
| chr5:138823956
|
CAAAA | C | 76 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(73): Show | 76 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.589-547_589-544del others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | |||||
| chr5:138823956
|
CAAAAA | C | 11 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0001g0151others(8): Show | 11 | HG00639.hp2 HG01070.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.589-548_589-544del others(5): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | |||||
| chr5:138823956
|
CAAAAAAA others(7): Show |
C | 25 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(22): Show | 25 | HG00438.hp2 HG00741.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.589-557_589-544del others(14): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | |||||
| chr5:138824111
|
G | A | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-419G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138824111 | ||||||
| chr5:138824130
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.589-400C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138824130 | ||||||
| chr5:138824177
|
A | G | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.589-353A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138824177 | ||||||
| chr5:138824282
|
A | G | 1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.589-248A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138824282 | ||||||
| chr5:138824322
|
G | C | 3 | a0001c0002t0003g0032a0001c0002t0003g0033a0001c0002t0003g0034 | 3 | HG00741.hp1 HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.589-208G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138824322 | ||||||
| chr5:138824367
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.589-163A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138824367 | ||||||
| chr5:138825062
|
G | T | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.858+263G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138825062 | ||||||
| chr5:138825209
|
G | A | 4 | a0001c0002t0002g0058a0001c0002t0002g0066a0001c0002t0002g0067others(1): Show | 4 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(1): Show |
intron_variant | MODIFIER | c.858+410G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138825209 | ||||||
| chr5:138825482
|
G | GTTTTTT | 7 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(4): Show | 7 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.858+694_858+699dup others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | |||||
| chr5:138825482
|
G | GTTTTTTT others(3): Show |
2 | a0001c0001t0006g0174a0001c0001t0006g0175 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.858+690_858+699dup others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | |||||
| chr5:138825482
|
G | GTTTTTTT others(5): Show |
13 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(10): Show | 13 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.858+688_858+699dup others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | |||||
| chr5:138825482
|
G | GTTTTTTT others(6): Show |
8 | a0001c0001t0001g0014a0001c0001t0001g0114a0001c0001t0001g0115others(5): Show | 8 | HG02132.hp1 HG02602.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.858+687_858+699dup others(13): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | |||||
| chr5:138825482
|
G | GTTTTTTT others(7): Show |
16 | a0001c0001t0001g0011a0001c0001t0001g0101a0001c0001t0001g0102others(13): Show | 16 | HG00639.hp2 HG01070.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.858+686_858+699dup others(14): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | |||||
| chr5:138825482
|
G | GTTTTTTT others(8): Show |
30 | a0001c0001t0001g0037a0001c0001t0001g0087a0001c0001t0001g0098others(27): Show | 30 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.858+685_858+699dup others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | |||||
| chr5:138825482
|
G | GTTTTTTT others(9): Show |
20 | a0001c0001t0001g0036a0001c0001t0001g0106a0001c0001t0001g0108others(17): Show | 20 | HG00735.hp2 HG01109.hp1 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.858+684_858+699dup others(16): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | |||||
| chr5:138825482
|
G | GTTTTTTT others(10): Show |
16 | a0001c0001t0001g0038a0001c0001t0001g0086a0001c0001t0001g0089others(13): Show | 16 | HG00423.hp2 HG01167.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.858+699_858+700ins others(17): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | |||||
| chr5:138825482
|
G | GTTTTTTT others(11): Show |
8 | a0001c0001t0001g0104a0001c0001t0001g0142a0001c0002t0003g0027others(5): Show | 8 | HG00423.hp1 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.858+699_858+700ins others(18): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | |||||
| chr5:138825482
|
G | GTTTTTTT others(12): Show |
9 | a0001c0001t0001g0039a0001c0001t0001g0092a0001c0002t0003g0004others(6): Show | 9 | HG00741.hp1 HG01243.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.858+699_858+700ins others(19): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | |||||
| chr5:138825482
|
G | GTTTTTTT others(13): Show |
5 | a0001c0001t0001g0041a0001c0001t0001g0045a0001c0001t0001g0097others(2): Show | 5 | HG01243.hp2 HG02129.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.858+699_858+700ins others(20): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | |||||
| chr5:138825482
|
G | GTTTTTTT others(16): Show |
1 | a0001c0001t0001g0046 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.858+699_858+700ins others(23): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | |||||
| chr5:138825482
|
G | GTTTTTTT others(18): Show |
1 | a0001c0002t0003g0029 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.858+699_858+700ins others(25): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | |||||
| chr5:138825482
|
G | GTTTTTTT others(22): Show |
1 | a0001c0002t0008g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.858+699_858+700ins others(29): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | |||||
| chr5:138825529
|
TA | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.858+744delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825529 | |||||
| chr5:138825529
|
TAA | T | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.858+743_858+744del others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825529 | |||||
| chr5:138825775
|
A | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0097 | 2 | HG01243.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.858+976A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138825775 | ||||||
| chr5:138825906
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.858+1107G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138825906 | ||||||
| chr5:138826090
|
T | G | 1 | a0001c0003t0002g0064 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.858+1291T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138826090 | ||||||
| chr5:138826440
|
T | C | 95 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.859-1075T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138826440 | ||||||
| chr5:138826444
|
G | T | 1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.859-1071G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138826444 | ||||||
| chr5:138826525
|
AG | A | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.859-987delG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138826525 | |||||
| chr5:138826536
|
G | C | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.859-979G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138826536 | ||||||
| chr5:138826586
|
G | A | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.859-929G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138826586 | ||||||
| chr5:138827083
|
G | A | 83 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.859-432G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138827083 | ||||||
| chr5:138827158
|
G | A | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.859-357G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138827158 | ||||||
| chr5:138827361
|
G | GT | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.859-153dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138827361 | |||||
| chr5:138827499
|
A | G | 1 | a0001c0001t0001g0045 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.859-16A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138827499 | ||||||
| chr5:138827887
|
T | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+169T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138827887 | ||||||
| chr5:138827970
|
A | G | 1 | a0001c0002t0002g0002 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1062+252A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138827970 | ||||||
| chr5:138827970
|
A | T | 14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1062+252A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138827970 | ||||||
| chr5:138827987
|
T | C | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+269T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138827987 | ||||||
| chr5:138828026
|
G | GT | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1062+308_1062+309i others(3): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138828026 | ||||||
| chr5:138828027
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0164 | 2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1062+309G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138828027 | ||||||
| chr5:138828032
|
T | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1062+314T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138828032 | ||||||
| chr5:138828164
|
A | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1062+446A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138828164 | ||||||
| chr5:138828310
|
A | G | 3 | a0001c0002t0003g0029a0001c0002t0008g0028a0001c0013t0003g0031 | 3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1062+592A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138828310 | ||||||
| chr5:138828370
|
C | CT | 63 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(60): Show | 63 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1062+661dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138828370 | |||||
| chr5:138828398
|
C | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1062+680C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138828398 | ||||||
| chr5:138828428
|
A | G | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+710A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138828428 | ||||||
| chr5:138828618
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+900C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138828618 | ||||||
| chr5:138828767
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1062+1049C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138828767 | ||||||
| chr5:138829037
|
G | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+1319G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138829037 | ||||||
| chr5:138829077
|
G | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1062+1359G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138829077 | ||||||
| chr5:138829315
|
G | A | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+1597G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138829315 | ||||||
| chr5:138829378
|
G | A | 1 | a0001c0002t0003g0024 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1062+1660G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138829378 | ||||||
| chr5:138829528
|
T | C | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1062+1810T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138829528 | ||||||
| chr5:138829562
|
T | G | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1062+1844T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138829562 | ||||||
| chr5:138829897
|
G | C | 10 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(7): Show | 10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1062+2179G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138829897 | ||||||
| chr5:138829962
|
A | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1062+2244A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138829962 | ||||||
| chr5:138830166
|
C | CA | 24 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(21): Show | 24 | HG00438.hp2 HG00741.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1062+2461dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138830166 | |||||
| chr5:138830166
|
CA | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1062+2461delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138830166 | |||||
| chr5:138830482
|
C | T | 4 | a0001c0001t0001g0131a0001c0001t0001g0136a0001c0001t0001g0140others(1): Show | 4 | HG02258.hp2 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1062+2764C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138830482 | ||||||
| chr5:138830683
|
A | G | 12 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(9): Show | 12 | HG00423.hp2 HG01243.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1062+2965A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138830683 | ||||||
| chr5:138830787
|
AACAG | A | 2 | a0001c0001t0006g0174a0001c0001t0006g0175 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+3073_1062+307 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138830787 | |||||
| chr5:138830795
|
A | G | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1062+3077A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138830795 | ||||||
| chr5:138830818
|
G | C | 1 | a0001c0001t0001g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1062+3100G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138830818 | ||||||
| chr5:138830998
|
A | G | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+3280A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138830998 | ||||||
| chr5:138831072
|
CATT | C | 2 | a0001c0001t0006g0174a0001c0001t0006g0175 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+3355_1062+335 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138831072 | ||||||
| chr5:138831081
|
A | G | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+3363A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138831081 | ||||||
| chr5:138831325
|
C | T | 3 | a0001c0002t0003g0020a0001c0002t0003g0025a0001c0012t0003g0019 | 3 | HG02280.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1062+3607C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138831325 | ||||||
| chr5:138831416
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1062+3698T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138831416 | ||||||
| chr5:138831581
|
T | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+3863T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138831581 | ||||||
| chr5:138831599
|
G | T | 1 | a0001c0001t0001g0124 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1062+3881G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138831599 | ||||||
| chr5:138831808
|
A | G | 78 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1062+4090A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138831808 | ||||||
| chr5:138831940
|
A | G | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+4222A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138831940 | ||||||
| chr5:138832077
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1062+4359G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138832077 | ||||||
| chr5:138832351
|
C | T | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1062+4633C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138832351 | ||||||
| chr5:138832459
|
A | T | 1 | a0001c0001t0001g0177 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1062+4741A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138832459 | ||||||
| chr5:138832727
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1062+5009T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138832727 | ||||||
| chr5:138832838
|
A | G | 6 | a0001c0001t0001g0102a0001c0001t0001g0114a0001c0001t0001g0115others(3): Show | 6 | HG02132.hp1 HG02602.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1062+5120A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138832838 | ||||||
| chr5:138833095
|
A | G | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1062+5377A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138833095 | ||||||
| chr5:138833243
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1062+5525C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138833243 | ||||||
| chr5:138833410
|
T | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.1062+5692T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138833410 | ||||||
| chr5:138833534
|
C | T | 14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1062+5816C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138833534 | ||||||
| chr5:138833581
|
A | G | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1062+5863A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138833581 | ||||||
| chr5:138833597
|
T | C | 1 | a0001c0001t0006g0174 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1062+5879T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138833597 | ||||||
| chr5:138833839
|
A | C | 1 | a0001c0002t0002g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1062+6121A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138833839 | ||||||
| chr5:138833874
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1062+6156G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138833874 | ||||||
| chr5:138833990
|
T | G | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1062+6272T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138833990 | ||||||
| chr5:138834104
|
A | G | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+6386A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138834104 | ||||||
| chr5:138834205
|
A | G | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+6487A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138834205 | ||||||
| chr5:138834241
|
A | C | 1 | a0001c0002t0005g0050 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1062+6523A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138834241 | ||||||
| chr5:138834770
|
G | A | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+7052G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138834770 | ||||||
| chr5:138834793
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1062+7075T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138834793 | ||||||
| chr5:138835338
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1062+7620C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138835338 | ||||||
| chr5:138835377
|
C | T | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+7659C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138835377 | ||||||
| chr5:138835513
|
G | A | 2 | a0001c0004t0004g0005a0001c0009t0004g0006 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1062+7795G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138835513 | ||||||
| chr5:138835718
|
C | T | 2 | a0001c0001t0006g0174a0001c0001t0006g0175 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+8000C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138835718 | ||||||
| chr5:138835734
|
T | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+8016T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138835734 | ||||||
| chr5:138835812
|
G | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+8094G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138835812 | ||||||
| chr5:138836047
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1062+8329C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138836047 | ||||||
| chr5:138836203
|
A | G | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1062+8485A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138836203 | ||||||
| chr5:138836307
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+8589A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138836307 | ||||||
| chr5:138836384
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1062+8666A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138836384 | ||||||
| chr5:138836531
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+8813C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138836531 | ||||||
| chr5:138836810
|
C | G | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1062+9092C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138836810 | ||||||
| chr5:138837463
|
C | T | 1 | a0001c0002t0002g0079 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1062+9745C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138837463 | ||||||
| chr5:138837537
|
C | G | 2 | a0001c0002t0002g0075a0001c0002t0002g0084 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1062+9819C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138837537 | ||||||
| chr5:138837693
|
C | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+9975C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138837693 | ||||||
| chr5:138837867
|
G | C | 3 | a0001c0001t0001g0103a0001c0001t0001g0160a0001c0001t0001g0171 | 3 | HG00639.hp2 HG01361.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1062+10149G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138837867 | ||||||
| chr5:138837904
|
G | A | 2 | a0002c0006t0001g0090a0002c0006t0001g0095 | 2 | NA19057.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1062+10186G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138837904 | ||||||
| chr5:138838101
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1062+10383A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138838101 | ||||||
| chr5:138838447
|
T | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1062+10729T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138838447 | ||||||
| chr5:138838530
|
A | AT | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+10821dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138838530 | |||||
| chr5:138838789
|
G | T | 12 | a0001c0002t0002g0056a0001c0002t0002g0060a0001c0002t0003g0020others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1062+11071G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138838789 | ||||||
| chr5:138838831
|
G | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+11113G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138838831 | ||||||
| chr5:138838858
|
T | G | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+11140T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138838858 | ||||||
| chr5:138838911
|
G | A | 10 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(7): Show | 10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1062+11193G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138838911 | ||||||
| chr5:138838932
|
A | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02257.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1062+11214A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138838932 | ||||||
| chr5:138839070
|
T | C | 32 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(29): Show | 32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1062+11352T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138839070 | ||||||
| chr5:138839224
|
A | AT | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+11516dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138839224 | |||||
| chr5:138839538
|
T | G | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+11820T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138839538 | ||||||
| chr5:138839568
|
A | G | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1062+11850A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138839568 | ||||||
| chr5:138839660
|
T | A | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1062+11942T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138839660 | ||||||
| chr5:138839680
|
A | G | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+11962A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138839680 | ||||||
| chr5:138839753
|
A | G | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1062+12035A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138839753 | ||||||
| chr5:138840137
|
T | C | 3 | a0001c0002t0005g0026a0001c0002t0005g0050a0001c0002t0005g0068 | 3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1062+12419T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138840137 | ||||||
| chr5:138840184
|
G | A | 1 | a0003c0007t0001g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1062+12466G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138840184 | ||||||
| chr5:138840221
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+12503G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138840221 | ||||||
| chr5:138840715
|
T | TAGAAATG others(46): Show |
1 | a0001c0001t0001g0001 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1062+12997_1062+12 others(59): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138840715 | ||||||
| chr5:138840716
|
T | A | 1 | a0001c0001t0001g0001 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1062+12998T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138840716 | ||||||
| chr5:138840717
|
T | A | 1 | a0001c0001t0001g0001 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1062+12999T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138840717 | ||||||
| chr5:138840718
|
T | A | 1 | a0001c0001t0001g0001 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1062+13000T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138840718 | ||||||
| chr5:138840769
|
G | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+13051G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138840769 | ||||||
| chr5:138841000
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+13282C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138841000 | ||||||
| chr5:138841265
|
T | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+13547T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138841265 | ||||||
| chr5:138841432
|
G | A | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1062+13714G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138841432 | ||||||
| chr5:138841459
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1062+13741C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138841459 | ||||||
| chr5:138841572
|
G | A | 32 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(29): Show | 32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1062+13854G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138841572 | ||||||
| chr5:138841631
|
CA | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+13917delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138841631 | |||||
| chr5:138841641
|
A | G | 2 | a0001c0001t0001g0042a0001c0001t0001g0045 | 2 | NA18983.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1062+13923A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138841641 | ||||||
| chr5:138841715
|
A | G | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+13997A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138841715 | ||||||
| chr5:138841757
|
G | A | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1062+14039G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138841757 | ||||||
| chr5:138841946
|
A | G | 1 | a0001c0002t0002g0061 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1062+14228A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138841946 | ||||||
| chr5:138842057
|
T | G | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0165 | 3 | HG02970.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1062+14339T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138842057 | ||||||
| chr5:138842659
|
C | T | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0165 | 3 | HG02970.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1062+14941C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138842659 | ||||||
| chr5:138842697
|
C | T | 1 | a0001c0002t0002g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1062+14979C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138842697 | ||||||
| chr5:138842703
|
A | G | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1062+14985A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138842703 | ||||||
| chr5:138842799
|
A | G | 9 | a0001c0002t0003g0004a0001c0002t0003g0032a0001c0002t0003g0033others(6): Show | 9 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1062+15081A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138842799 | ||||||
| chr5:138842913
|
C | G | 1 | a0001c0001t0001g0108 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1062+15195C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138842913 | ||||||
| chr5:138843482
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1062+15764C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138843482 | ||||||
| chr5:138843891
|
A | G | 25 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(22): Show | 25 | HG00438.hp2 HG00741.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1062+16173A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138843891 | ||||||
| chr5:138843950
|
G | A | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1062+16232G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138843950 | ||||||
| chr5:138843968
|
C | T | 1 | a0001c0003t0002g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1062+16250C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138843968 | ||||||
| chr5:138844049
|
A | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+16331A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138844049 | ||||||
| chr5:138844093
|
T | TTA | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+16375_1062+16 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138844093 | ||||||
| chr5:138844094
|
G | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+16376G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138844094 | ||||||
| chr5:138844204
|
C | T | 95 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1062+16486C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138844204 | ||||||
| chr5:138844245
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1062+16527C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138844245 | ||||||
| chr5:138844627
|
G | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+16909G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138844627 | ||||||
| chr5:138844769
|
TTATG | T | 10 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(7): Show | 10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1062+17055_1062+17 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138844769 | |||||
| chr5:138845075
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1062+17357T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138845075 | ||||||
| chr5:138845518
|
A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0123 | 2 | HG00099.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1062+17800A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138845518 | ||||||
| chr5:138845583
|
G | A | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1062+17865G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138845583 | ||||||
| chr5:138845594
|
C | CATTT | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+17877_1062+17 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138845594 | |||||
| chr5:138845729
|
A | G | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+18011A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138845729 | ||||||
| chr5:138845773
|
T | G | 4 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1062+18055T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138845773 | ||||||
| chr5:138845784
|
T | A | 2 | a0001c0001t0007g0111a0001c0001t0007g0112 | 2 | HG01099.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.1062+18066T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138845784 | ||||||
| chr5:138845869
|
C | A | 1 | a0001c0001t0001g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1062+18151C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138845869 | ||||||
| chr5:138845874
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+18156A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138845874 | ||||||
| chr5:138845885
|
G | A | 5 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(2): Show | 5 | HG01109.hp2 HG01993.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+18167G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138845885 | ||||||
| chr5:138845915
|
TTTTTTTG others(8): Show |
T | 94 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.1062+18213_1062+18 others(21): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138845915 | |||||
| chr5:138845916
|
TTTTTTGT others(7): Show |
T | 1 | a0001c0001t0001g0123 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1062+18204_1062+18 others(20): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138845916 | |||||
| chr5:138845939
|
T | C | 1 | a0001c0002t0002g0054 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1062+18221T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138845939 | ||||||
| chr5:138846013
|
G | A | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1062+18295G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138846013 | ||||||
| chr5:138846177
|
C | T | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+18459C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138846177 | ||||||
| chr5:138846213
|
A | G | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1062+18495A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138846213 | ||||||
| chr5:138846216
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1062+18498T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138846216 | ||||||
| chr5:138846318
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+18600A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138846318 | ||||||
| chr5:138846542
|
A | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018 | 3 | HG02257.hp1 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1062+18824A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138846542 | ||||||
| chr5:138846639
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+18921C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138846639 | ||||||
| chr5:138846768
|
A | T | 95 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1062+19050A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138846768 | ||||||
| chr5:138846769
|
C | A | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1062+19051C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138846769 | ||||||
| chr5:138846841
|
C | T | 95 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1062+19123C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138846841 | ||||||
| chr5:138847122
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1062+19404A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138847122 | ||||||
| chr5:138847166
|
A | G | 1 | a0001c0001t0006g0174 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1062+19448A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138847166 | ||||||
| chr5:138847297
|
T | TA | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+19580dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138847297 | |||||
| chr5:138847475
|
A | C | 1 | a0001c0002t0002g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1062+19757A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138847475 | ||||||
| chr5:138847640
|
G | A | 2 | a0001c0002t0002g0002a0001c0002t0002g0003 | 2 | HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1062+19922G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138847640 | ||||||
| chr5:138848101
|
C | T | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1062+20383C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138848101 | ||||||
| chr5:138848150
|
A | G | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+20432A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138848150 | ||||||
| chr5:138848168
|
T | TG | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1062+20450_1062+20 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138848168 | ||||||
| chr5:138848399
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1062+20681G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138848399 | ||||||
| chr5:138848735
|
T | G | 1 | a0001c0001t0001g0104 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1062+21017T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138848735 | ||||||
| chr5:138848985
|
T | A | 10 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(7): Show | 10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1062+21267T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138848985 | ||||||
| chr5:138849092
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1062+21374A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849092 | ||||||
| chr5:138849228
|
T | C | 4 | a0001c0001t0001g0088a0001c0001t0001g0149a0003c0007t0001g0099others(1): Show | 4 | HG02723.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1062+21510T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849228 | ||||||
| chr5:138849273
|
A | T | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1062+21555A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849273 | ||||||
| chr5:138849279
|
A | T | 1 | a0001c0002t0003g0024 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1062+21561A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849279 | ||||||
| chr5:138849333
|
A | G | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1062+21615A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849333 | ||||||
| chr5:138849456
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1062+21738A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849456 | ||||||
| chr5:138849594
|
G | A | 1 | a0001c0002t0003g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1062+21876G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849594 | ||||||
| chr5:138849604
|
C | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+21886C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849604 | ||||||
| chr5:138849727
|
A | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1062+22009A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849727 | ||||||
| chr5:138849815
|
G | A | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1062+22097G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849815 | ||||||
| chr5:138849937
|
T | C | 3 | a0001c0001t0001g0153a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | HG01074.hp2 HG01081.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1062+22219T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849937 | ||||||
| chr5:138849989
|
A | AAC | 3 | a0001c0001t0001g0132a0001c0001t0001g0143a0001c0001t0001g0150 | 3 | HG02630.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1062+22288_1062+22 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138849989 | |||||
| chr5:138849989
|
A | AACAC | 18 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(15): Show | 18 | HG02257.hp1 HG02280.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1062+22286_1062+22 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138849989 | |||||
| chr5:138849989
|
A | AACACAC | 4 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1062+22284_1062+22 others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138849989 | |||||
| chr5:138850272
|
CCTGGATG others(9): Show |
C | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+22557_1062+22 others(22): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138850272 | |||||
| chr5:138850353
|
A | C | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0165 | 3 | HG02970.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1062+22635A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138850353 | ||||||
| chr5:138850618
|
C | G | 3 | a0001c0002t0003g0020a0001c0002t0003g0025a0001c0012t0003g0019 | 3 | HG02280.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1062+22900C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138850618 | ||||||
| chr5:138850667
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0017 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1062+22949A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138850667 | ||||||
| chr5:138850784
|
T | TC | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+23067dupC | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138850784 | |||||
| chr5:138850895
|
A | T | 1 | a0001c0002t0003g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1062+23177A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138850895 | ||||||
| chr5:138851018
|
G | T | 1 | a0001c0002t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1062+23300G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138851018 | ||||||
| chr5:138851075
|
T | G | 2 | a0001c0004t0004g0005a0001c0009t0004g0006 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1062+23357T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138851075 | ||||||
| chr5:138851808
|
T | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.1062+24090T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138851808 | ||||||
| chr5:138852058
|
G | A | 2 | a0001c0002t0002g0066a0001c0002t0002g0083 | 2 | HG00639.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.1062+24340G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852058 | ||||||
| chr5:138852202
|
A | G | 1 | a0001c0002t0003g0033 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1062+24484A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852202 | ||||||
| chr5:138852351
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1062+24633C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852351 | ||||||
| chr5:138852463
|
T | TG | 14 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0091others(11): Show | 14 | HG00423.hp2 HG01891.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1062+24753dupG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852463 | |||||
| chr5:138852565
|
C | T | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1062+24847C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852565 | ||||||
| chr5:138852686
|
A | G | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1062+24968A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852686 | ||||||
| chr5:138852723
|
T | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0165 | 3 | HG02970.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1062+25005T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852723 | ||||||
| chr5:138852772
|
C | T | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+25054C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852772 | ||||||
| chr5:138852859
|
T | TCGCGCGC others(20): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0016 | 2 | HG02559.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1062+25148_1062+25 others(33): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852859 | |||||
| chr5:138852859
|
T | TCGCGCGC others(17): Show |
1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1062+25150_1062+25 others(30): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852859 | |||||
| chr5:138852859
|
T | TCGCGCGC others(17): Show |
4 | a0001c0001t0001g0139a0001c0001t0006g0174a0001c0001t0006g0175others(1): Show | 4 | HG01884.hp2 HG03225.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1062+25152_1062+25 others(30): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852859 | |||||
| chr5:138852859
|
T | TCGCGCGC others(19): Show |
88 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(85): Show | 88 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1062+25152_1062+25 others(32): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852859 | |||||
| chr5:138852859
|
T | TCGCGCGC others(21): Show |
1 | a0001c0001t0001g0179 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1062+25152_1062+25 others(34): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852859 | |||||
| chr5:138852859
|
T | TCGCGCGT others(19): Show |
12 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0091others(9): Show | 12 | HG00423.hp2 HG01243.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1062+25147_1062+25 others(32): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852859 | |||||
| chr5:138852860
|
C | T | 3 | a0001c0002t0003g0029a0001c0002t0008g0028a0001c0013t0003g0031 | 3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1062+25142C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852860 | ||||||
| chr5:138852863
|
G | GCGCGCGC others(19): Show |
3 | a0001c0005t0001g0156a0001c0005t0001g0167a0001c0005t0001g0168 | 3 | HG00099.hp1 HG00741.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1062+25152_1062+25 others(32): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852863 | |||||
| chr5:138852868
|
C | CGCACGCG others(19): Show |
1 | a0001c0001t0001g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1062+25152_1062+25 others(32): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852868 | |||||
| chr5:138852871
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1062+25153G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852871 | ||||||
| chr5:138852871
|
G | GCACGCGC others(21): Show |
2 | a0001c0001t0001g0129a0001c0001t0001g0137 | 2 | HG00642.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1062+25156_1062+25 others(34): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852871 | |||||
| chr5:138852871
|
G | GCGCGCGC others(21): Show |
1 | a0001c0001t0001g0123 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1062+25154_1062+25 others(34): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852871 | |||||
| chr5:138852873
|
A | G | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1062+25155A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852873 | ||||||
| chr5:138852981
|
C | T | 1 | a0001c0004t0004g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1062+25263C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852981 | ||||||
| chr5:138853022
|
G | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+25304G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138853022 | ||||||
| chr5:138853107
|
A | C | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+25389A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138853107 | ||||||
| chr5:138853166
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+25448C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138853166 | ||||||
| chr5:138853264
|
T | G | 3 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | HG02074.hp2 NA18983.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1062+25546T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138853264 | ||||||
| chr5:138853495
|
T | TA | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1062+25790dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138853495 | |||||
| chr5:138853582
|
T | G | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+25864T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138853582 | ||||||
| chr5:138853585
|
G | A | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+25867G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138853585 | ||||||
| chr5:138853663
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0123 | 2 | HG00099.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1062+25945G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138853663 | ||||||
| chr5:138853846
|
T | C | 1 | a0001c0002t0003g0048 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1062+26128T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138853846 | ||||||
| chr5:138853891
|
G | T | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1062+26173G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138853891 | ||||||
| chr5:138854009
|
A | G | 1 | a0001c0009t0004g0006 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1062+26291A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138854009 | ||||||
| chr5:138854311
|
CAG | C | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+26594_1062+26 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138854311 | ||||||
| chr5:138854508
|
A | G | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1062+26790A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138854508 | ||||||
| chr5:138854588
|
G | A | 10 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(7): Show | 10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1062+26870G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138854588 | ||||||
| chr5:138854712
|
A | G | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1062+26994A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138854712 | ||||||
| chr5:138855097
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+27379A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138855097 | ||||||
| chr5:138855327
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1062+27609G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138855327 | ||||||
| chr5:138855685
|
G | A | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1062+27967G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138855685 | ||||||
| chr5:138855704
|
A | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+27986A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138855704 | ||||||
| chr5:138855750
|
T | C | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+28032T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138855750 | ||||||
| chr5:138855992
|
A | T | 2 | a0001c0004t0004g0005a0001c0009t0004g0006 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1062+28274A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138855992 | ||||||
| chr5:138856092
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1062+28374T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138856092 | ||||||
| chr5:138856349
|
T | A | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1062+28631T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138856349 | ||||||
| chr5:138856379
|
GT | G | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+28663delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138856379 | |||||
| chr5:138856470
|
T | C | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1062+28752T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138856470 | ||||||
| chr5:138856542
|
G | A | 3 | a0001c0002t0003g0029a0001c0002t0008g0028a0001c0013t0003g0031 | 3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1062+28824G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138856542 | ||||||
| chr5:138856727
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1062+29009G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138856727 | ||||||
| chr5:138856750
|
A | G | 1 | a0001c0002t0002g0065 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1062+29032A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138856750 | ||||||
| chr5:138856817
|
C | G | 3 | a0001c0004t0004g0005a0001c0004t0004g0180a0001c0009t0004g0006 | 3 | HG02486.hp2 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1062+29099C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138856817 | ||||||
| chr5:138856975
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1063-29237A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138856975 | ||||||
| chr5:138857243
|
T | G | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-28969T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138857243 | ||||||
| chr5:138857308
|
A | G | 3 | a0001c0002t0003g0029a0001c0002t0008g0028a0001c0013t0003g0031 | 3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1063-28904A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138857308 | ||||||
| chr5:138857487
|
A | T | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1063-28725A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138857487 | ||||||
| chr5:138857488
|
A | AT | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1063-28717dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138857488 | |||||
| chr5:138857488
|
A | T | 21 | a0001c0001t0001g0036a0001c0001t0001g0092a0001c0001t0001g0094others(18): Show | 21 | HG01099.hp2 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1063-28724A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138857488 | ||||||
| chr5:138857592
|
C | T | 1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1063-28620C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138857592 | ||||||
| chr5:138857687
|
G | A | 4 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063-28525G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138857687 | ||||||
| chr5:138857784
|
C | T | 1 | a0001c0001t0006g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1063-28428C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138857784 | ||||||
| chr5:138857826
|
A | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1063-28386A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138857826 | ||||||
| chr5:138857973
|
G | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-28239G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138857973 | ||||||
| chr5:138858076
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1063-28136C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138858076 | ||||||
| chr5:138858095
|
T | C | 1 | a0001c0002t0005g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1063-28117T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138858095 | ||||||
| chr5:138858120
|
TA | T | 5 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 5 | HG01070.hp1 HG01109.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1063-28084delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858120 | |||||
| chr5:138858128
|
AT | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.1063-28068delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858128 | |||||
| chr5:138858576
|
T | TTTTTTC | 17 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(14): Show | 17 | HG00423.hp2 HG02486.hp2 HG02735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1063-27618_1063-27 others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858576 | |||||
| chr5:138858576
|
T | TTTTTTCT others(5): Show |
2 | a0001c0001t0001g0097a0001c0004t0004g0007 | 2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1063-27624_1063-27 others(18): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858576 | |||||
| chr5:138858594
|
CT | C | 6 | a0001c0001t0001g0040a0001c0001t0001g0166a0001c0002t0002g0081others(3): Show | 6 | HG00438.hp2 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1063-27599delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858594 | |||||
| chr5:138858595
|
T | TTTTTC | 92 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.1063-27613_1063-27 others(11): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858595 | |||||
| chr5:138858595
|
T | TTTTTCTT others(4): Show |
4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(1): Show | 4 | HG02074.hp2 HG02129.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-27613_1063-27 others(17): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858595 | |||||
| chr5:138858595
|
T | TTTTTCTT others(16): Show |
9 | a0001c0002t0003g0004a0001c0002t0003g0032a0001c0002t0003g0033others(6): Show | 9 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1063-27613_1063-27 others(29): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858595 | |||||
| chr5:138858596
|
T | TTTTCTTT others(3): Show |
10 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(7): Show | 10 | HG01109.hp2 HG01993.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1063-27613_1063-27 others(16): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858596 | |||||
| chr5:138858596
|
T | TTTTCTTT others(9): Show |
1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1063-27613_1063-27 others(22): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858596 | |||||
| chr5:138858597
|
T | TTTCTTTT others(8): Show |
1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1063-27613_1063-27 others(21): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858597 | |||||
| chr5:138858676
|
A | C | 1 | a0001c0001t0001g0150 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1063-27536A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138858676 | ||||||
| chr5:138858700
|
A | G | 13 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(10): Show | 13 | HG00423.hp2 HG01243.hp2 HG03486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1063-27512A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138858700 | ||||||
| chr5:138859188
|
G | C | 3 | a0001c0002t0003g0020a0001c0002t0003g0025a0001c0012t0003g0019 | 3 | HG02280.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1063-27024G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138859188 | ||||||
| chr5:138859299
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.1063-26913C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138859299 | ||||||
| chr5:138859513
|
A | G | 1 | a0001c0002t0003g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1063-26699A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138859513 | ||||||
| chr5:138859528
|
T | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.1063-26684T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138859528 | ||||||
| chr5:138859624
|
G | A | 11 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(8): Show | 11 | HG00423.hp2 NA18946.hp1 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-26588G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138859624 | ||||||
| chr5:138859662
|
G | A | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-26550G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138859662 | ||||||
| chr5:138860104
|
A | G | 95 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1063-26108A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138860104 | ||||||
| chr5:138860128
|
A | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1063-26084A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138860128 | ||||||
| chr5:138860181
|
A | G | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1063-26031A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138860181 | ||||||
| chr5:138860463
|
C | A | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1063-25749C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138860463 | ||||||
| chr5:138860493
|
TTTG | T | 14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1063-25716_1063-25 others(9): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138860493 | |||||
| chr5:138860496
|
G | GTTTGT | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1063-25696_1063-25 others(11): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138860496 | |||||
| chr5:138860500
|
GT | G | 14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1063-25708delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138860500 | |||||
| chr5:138860584
|
C | T | 81 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.1063-25628C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138860584 | ||||||
| chr5:138860759
|
A | T | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1063-25453A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138860759 | ||||||
| chr5:138861042
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1063-25170C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138861042 | ||||||
| chr5:138861071
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1063-25141G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138861071 | ||||||
| chr5:138861285
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1063-24927T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138861285 | ||||||
| chr5:138861470
|
A | T | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-24742A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138861470 | ||||||
| chr5:138861517
|
C | G | 1 | a0001c0002t0008g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1063-24695C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138861517 | ||||||
| chr5:138862373
|
T | C | 2 | a0001c0003t0002g0062a0001c0003t0002g0064 | 2 | HG01346.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1063-23839T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138862373 | ||||||
| chr5:138862644
|
A | T | 1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1063-23568A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138862644 | ||||||
| chr5:138862655
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1063-23557T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138862655 | ||||||
| chr5:138862687
|
G | A | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1063-23525G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138862687 | ||||||
| chr5:138862900
|
G | T | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1063-23312G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138862900 | ||||||
| chr5:138863015
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1063-23197A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138863015 | ||||||
| chr5:138863182
|
T | G | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1063-23030T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138863182 | ||||||
| chr5:138863226
|
T | A | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1063-22986T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138863226 | ||||||
| chr5:138863360
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0017 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1063-22852C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138863360 | ||||||
| chr5:138863435
|
A | G | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-22777A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138863435 | ||||||
| chr5:138863490
|
C | T | 13 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(10): Show | 13 | HG00423.hp2 HG01243.hp2 HG03486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1063-22722C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138863490 | ||||||
| chr5:138863501
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1063-22711C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138863501 | ||||||
| chr5:138863671
|
G | A | 10 | a0001c0001t0001g0131a0001c0001t0001g0135a0001c0001t0001g0136others(7): Show | 10 | HG01071.hp2 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1063-22541G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138863671 | ||||||
| chr5:138863875
|
A | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1063-22337A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138863875 | ||||||
| chr5:138864212
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1063-22000A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138864212 | ||||||
| chr5:138864250
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1063-21962C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138864250 | ||||||
| chr5:138864285
|
G | A | 1 | a0001c0002t0005g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1063-21927G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138864285 | ||||||
| chr5:138864340
|
A | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1063-21872A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138864340 | ||||||
| chr5:138864481
|
C | A | 1 | a0001c0001t0001g0133 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1063-21731C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138864481 | ||||||
| chr5:138864546
|
A | G | 1 | a0001c0001t0001g0001 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1063-21666A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138864546 | ||||||
| chr5:138864638
|
A | G | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1063-21574A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138864638 | ||||||
| chr5:138864768
|
G | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1063-21444G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138864768 | ||||||
| chr5:138864796
|
TTTTTTG | T | 30 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(27): Show | 30 | HG00438.hp2 HG00741.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1063-21385_1063-21 others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138864796 | |||||
| chr5:138864797
|
TTTTTG | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1063-21410_1063-21 others(11): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138864797 | |||||
| chr5:138864797
|
TTTTTGTT others(4): Show |
T | 1 | a0001c0001t0001g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1063-21410_1063-21 others(17): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138864797 | |||||
| chr5:138864876
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0162 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1063-21336G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138864876 | ||||||
| chr5:138864877
|
C | T | 95 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1063-21335C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138864877 | ||||||
| chr5:138865091
|
C | T | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1063-21121C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138865091 | ||||||
| chr5:138865101
|
C | T | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1063-21111C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138865101 | ||||||
| chr5:138865244
|
C | T | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1063-20968C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138865244 | ||||||
| chr5:138865253
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.1063-20959C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138865253 | ||||||
| chr5:138865308
|
C | T | 3 | a0001c0002t0005g0026a0001c0002t0005g0050a0001c0002t0005g0068 | 3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1063-20904C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138865308 | ||||||
| chr5:138865602
|
G | A | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-20610G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138865602 | ||||||
| chr5:138865746
|
A | T | 1 | a0001c0014t0001g0145 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1063-20466A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138865746 | ||||||
| chr5:138866241
|
A | G | 1 | a0001c0002t0002g0057 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1063-19971A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138866241 | ||||||
| chr5:138866273
|
C | CATTT | 52 | a0001c0001t0001g0038a0001c0001t0001g0086a0001c0001t0001g0087others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1063-19886_1063-19 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866273 | |||||
| chr5:138866273
|
C | CATTTATT others(1): Show |
15 | a0001c0001t0001g0096a0001c0001t0001g0108a0001c0001t0001g0116others(12): Show | 15 | HG00099.hp1 HG00323.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1063-19890_1063-19 others(14): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866273 | |||||
| chr5:138866273
|
C | CATTTATT others(5): Show |
2 | a0001c0001t0001g0102a0001c0005t0001g0168 | 2 | HG03654.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1063-19894_1063-19 others(18): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866273 | |||||
| chr5:138866273
|
CATTT | C | 26 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(23): Show | 26 | HG00438.hp1 HG00438.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1063-19886_1063-19 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866273 | |||||
| chr5:138866273
|
CATTTATT others(1): Show |
C | 11 | a0001c0001t0001g0046a0001c0001t0001g0097a0001c0001t0001g0103others(8): Show | 11 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1063-19890_1063-19 others(14): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866273 | |||||
| chr5:138866273
|
CATTTATT others(5): Show |
C | 3 | a0001c0001t0001g0037a0001c0001t0001g0120a0001c0004t0004g0007 | 3 | HG01993.hp2 HG03492.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1063-19894_1063-19 others(18): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866273 | |||||
| chr5:138866273
|
CATTTATT others(9): Show |
C | 1 | a0001c0001t0001g0160 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1063-19898_1063-19 others(22): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866273 | |||||
| chr5:138866273
|
CATTTATT others(13): Show |
C | 11 | a0001c0002t0003g0004a0001c0002t0003g0032a0001c0002t0003g0033others(8): Show | 11 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-19902_1063-19 others(26): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866273 | |||||
| chr5:138866289
|
T | TATTA | 2 | a0001c0002t0002g0080a0001c0002t0002g0081 | 2 | HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1063-19920_1063-19 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866289 | |||||
| chr5:138866310
|
A | AT | 8 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1063-19899dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866310 | |||||
| chr5:138866310
|
A | ATTTAT | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp2 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-19899_1063-19 others(11): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866310 | |||||
| chr5:138866372
|
A | G | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-19840A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138866372 | ||||||
| chr5:138866483
|
A | G | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-19729A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138866483 | ||||||
| chr5:138866554
|
G | C | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-19658G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138866554 | ||||||
| chr5:138866680
|
C | T | 2 | a0001c0001t0001g0109a0001c0002t0002g0073 | 2 | HG02735.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1063-19532C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138866680 | ||||||
| chr5:138866796
|
A | G | 11 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(8): Show | 11 | HG00423.hp2 NA18946.hp1 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-19416A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138866796 | ||||||
| chr5:138867027
|
A | T | 9 | a0001c0002t0002g0056a0001c0002t0002g0057a0001c0002t0002g0058others(6): Show | 9 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1063-19185A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138867027 | ||||||
| chr5:138867109
|
T | C | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1063-19103T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138867109 | ||||||
| chr5:138867344
|
C | T | 3 | a0001c0002t0002g0061a0001c0002t0002g0073a0001c0002t0002g0085 | 3 | HG01361.hp2 HG02735.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1063-18868C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138867344 | ||||||
| chr5:138867345
|
T | G | 65 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(62): Show | 65 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1063-18867T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138867345 | ||||||
| chr5:138867360
|
A | G | 11 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(8): Show | 11 | HG00423.hp2 NA18946.hp1 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-18852A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138867360 | ||||||
| chr5:138867575
|
T | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1063-18637T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138867575 | ||||||
| chr5:138867743
|
C | T | 4 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063-18469C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138867743 | ||||||
| chr5:138867743
|
CTTTCTTT others(7): Show |
C | 1 | a0001c0002t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1063-18455_1063-18 others(20): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138867743 | |||||
| chr5:138867747
|
C | CT | 17 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(14): Show | 17 | HG00423.hp2 HG01243.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1063-18452dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138867747 | |||||
| chr5:138867747
|
CT | C | 63 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(60): Show | 63 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1063-18452delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138867747 | |||||
| chr5:138867760
|
T | C | 3 | a0001c0001t0001g0153a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | HG01074.hp2 HG01081.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1063-18452T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138867760 | ||||||
| chr5:138868294
|
C | T | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-17918C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138868294 | ||||||
| chr5:138868322
|
T | C | 69 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(66): Show | 69 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1063-17890T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138868322 | ||||||
| chr5:138868418
|
G | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0164 | 2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1063-17794G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138868418 | ||||||
| chr5:138868567
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1063-17645C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138868567 | ||||||
| chr5:138868730
|
T | C | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-17482T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138868730 | ||||||
| chr5:138868792
|
A | G | 29 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0110others(26): Show | 29 | HG00099.hp2 HG00323.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1063-17420A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138868792 | ||||||
| chr5:138869173
|
T | TA | 23 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0001t0001g0104others(20): Show | 23 | HG00423.hp1 HG01099.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1063-17022dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138869173 | |||||
| chr5:138869173
|
T | TAA | 35 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(32): Show | 35 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1063-17023_1063-17 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138869173 | |||||
| chr5:138869173
|
TA | T | 15 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(12): Show | 15 | HG00423.hp2 HG00642.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1063-17022delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138869173 | |||||
| chr5:138869205
|
A | T | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1063-17007A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138869205 | ||||||
| chr5:138869272
|
A | T | 1 | a0001c0002t0003g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1063-16940A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138869272 | ||||||
| chr5:138869374
|
C | CT | 11 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(8): Show | 11 | HG00423.hp2 HG03516.hp1 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-16823dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138869374 | |||||
| chr5:138869374
|
CT | C | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1063-16823delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138869374 | |||||
| chr5:138869459
|
G | A | 1 | a0001c0002t0003g0021 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1063-16753G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138869459 | ||||||
| chr5:138869744
|
G | A | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1063-16468G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138869744 | ||||||
| chr5:138870187
|
C | T | 5 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 5 | HG01070.hp1 HG01109.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1063-16025C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138870187 | ||||||
| chr5:138870511
|
G | T | 69 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(66): Show | 69 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1063-15701G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138870511 | ||||||
| chr5:138870612
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1063-15600C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138870612 | ||||||
| chr5:138870786
|
A | C | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1063-15426A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138870786 | ||||||
| chr5:138871403
|
C | T | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1063-14809C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138871403 | ||||||
| chr5:138871550
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1063-14662C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138871550 | ||||||
| chr5:138871791
|
A | T | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1063-14421A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138871791 | ||||||
| chr5:138871844
|
G | A | 69 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(66): Show | 69 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1063-14368G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138871844 | ||||||
| chr5:138872022
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1063-14190G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138872022 | ||||||
| chr5:138872027
|
A | AGT | 16 | a0001c0001t0001g0038a0001c0001t0001g0096a0001c0001t0001g0119others(13): Show | 16 | HG00099.hp1 HG00438.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1063-14145_1063-14 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138872027 | |||||
| chr5:138872027
|
A | AGTGT | 17 | a0001c0001t0001g0088a0001c0001t0001g0102a0001c0001t0001g0110others(14): Show | 17 | HG00099.hp2 HG00642.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1063-14147_1063-14 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138872027 | |||||
| chr5:138872027
|
AGT | A | 35 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(32): Show | 35 | HG00423.hp2 HG00741.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.1063-14145_1063-14 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138872027 | |||||
| chr5:138872027
|
AGTGT | A | 7 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0001g0101others(4): Show | 7 | HG00423.hp1 HG00639.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.1063-14147_1063-14 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138872027 | |||||
| chr5:138872027
|
AGTGTGTG others(5): Show |
A | 11 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(8): Show | 11 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1063-14155_1063-14 others(18): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138872027 | |||||
| chr5:138872057
|
TGTGTGTG others(5): Show |
T | 28 | a0001c0001t0001g0012a0001c0002t0002g0035a0001c0002t0002g0053others(25): Show | 28 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1063-14153_1063-14 others(18): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138872057 | |||||
| chr5:138872059
|
TGTGTGTG others(3): Show |
T | 26 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(23): Show | 26 | HG00438.hp2 HG00741.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.1063-14151_1063-14 others(16): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138872059 | |||||
| chr5:138872061
|
TGTGTGTG others(1): Show |
T | 5 | a0001c0001t0001g0045a0001c0002t0003g0021a0001c0002t0003g0023others(2): Show | 5 | HG01109.hp2 HG01993.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063-14149_1063-14 others(14): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138872061 | |||||
| chr5:138872063
|
TGTGTGC | T | 2 | a0001c0002t0003g0025a0001c0012t0003g0019 | 2 | HG02280.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1063-14147_1063-14 others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138872063 | |||||
| chr5:138872065
|
TGTGC | T | 6 | a0001c0002t0003g0022a0001c0002t0003g0029a0001c0002t0008g0028others(3): Show | 6 | HG02723.hp1 HG02809.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1063-14145_1063-14 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138872065 | |||||
| chr5:138872067
|
T | C | 1 | a0002c0006t0001g0095 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1063-14145T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138872067 | ||||||
| chr5:138872069
|
C | T | 2 | a0001c0002t0003g0020a0001c0013t0003g0031 | 2 | HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1063-14143C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138872069 | ||||||
| chr5:138872420
|
G | A | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1063-13792G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138872420 | ||||||
| chr5:138872713
|
C | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1063-13499C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138872713 | ||||||
| chr5:138872751
|
C | T | 3 | a0001c0003t0002g0055a0001c0003t0002g0076a0001c0003t0002g0077 | 3 | HG00642.hp1 HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1063-13461C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138872751 | ||||||
| chr5:138872752
|
A | G | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1063-13460A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138872752 | ||||||
| chr5:138872778
|
T | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | NA18946.hp2 NA19003.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1063-13434T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138872778 | ||||||
| chr5:138872820
|
A | T | 4 | a0001c0001t0001g0131a0001c0001t0001g0136a0001c0001t0001g0140others(1): Show | 4 | HG02258.hp2 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-13392A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138872820 | ||||||
| chr5:138873064
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1063-13148A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138873064 | ||||||
| chr5:138873090
|
G | T | 1 | a0001c0001t0001g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1063-13122G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138873090 | ||||||
| chr5:138873439
|
A | G | 2 | a0002c0006t0001g0090a0002c0006t0001g0095 | 2 | NA19057.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1063-12773A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138873439 | ||||||
| chr5:138874363
|
C | T | 1 | a0001c0001t0001g0001 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1063-11849C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138874363 | ||||||
| chr5:138874798
|
A | C | 1 | a0001c0002t0002g0061 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1063-11414A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138874798 | ||||||
| chr5:138874814
|
T | C | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1063-11398T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138874814 | ||||||
| chr5:138874883
|
A | G | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1063-11329A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138874883 | ||||||
| chr5:138875206
|
C | A | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1063-11006C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138875206 | ||||||
| chr5:138875259
|
G | T | 1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1063-10953G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138875259 | ||||||
| chr5:138875283
|
G | C | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1063-10929G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138875283 | ||||||
| chr5:138875430
|
G | C | 1 | a0001c0001t0001g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1063-10782G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138875430 | ||||||
| chr5:138875495
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1063-10717C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138875495 | ||||||
| chr5:138875702
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1063-10510A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138875702 | ||||||
| chr5:138876240
|
G | T | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-9972G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138876240 | ||||||
| chr5:138876589
|
A | G | 5 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1063-9623A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138876589 | ||||||
| chr5:138876605
|
C | G | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1063-9607C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138876605 | ||||||
| chr5:138876728
|
A | T | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1063-9484A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138876728 | ||||||
| chr5:138876945
|
G | A | 1 | a0001c0002t0002g0053 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1063-9267G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138876945 | ||||||
| chr5:138877038
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1063-9174G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877038 | ||||||
| chr5:138877118
|
A | G | 2 | a0001c0004t0004g0005a0001c0009t0004g0006 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1063-9094A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877118 | ||||||
| chr5:138877143
|
T | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1063-9069T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877143 | ||||||
| chr5:138877441
|
C | CT | 39 | a0001c0001t0001g0046a0001c0001t0001g0139a0001c0001t0001g0176others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1063-8754dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138877441 | |||||
| chr5:138877479
|
C | T | 3 | a0001c0002t0005g0026a0001c0002t0005g0050a0001c0002t0005g0068 | 3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1063-8733C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877479 | ||||||
| chr5:138877512
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1063-8700A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877512 | ||||||
| chr5:138877541
|
G | A | 10 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(7): Show | 10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1063-8671G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877541 | ||||||
| chr5:138877549
|
G | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-8663G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877549 | ||||||
| chr5:138877603
|
A | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 84 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.1063-8609A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877603 | ||||||
| chr5:138877606
|
C | T | 11 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0117others(8): Show | 11 | HG00099.hp2 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-8606C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877606 | ||||||
| chr5:138877608
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1063-8604C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877608 | ||||||
| chr5:138877742
|
C | T | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1063-8470C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877742 | ||||||
| chr5:138877917
|
A | G | 1 | a0001c0002t0002g0085 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1063-8295A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877917 | ||||||
| chr5:138877975
|
G | A | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1063-8237G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877975 | ||||||
| chr5:138878177
|
T | A | 3 | a0001c0002t0005g0026a0001c0002t0005g0050a0001c0002t0005g0068 | 3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1063-8035T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138878177 | ||||||
| chr5:138878405
|
T | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 84 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.1063-7807T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138878405 | ||||||
| chr5:138878439
|
C | T | 2 | a0001c0001t0006g0174a0001c0001t0006g0175 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1063-7773C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138878439 | ||||||
| chr5:138879048
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1063-7164G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138879048 | ||||||
| chr5:138879171
|
T | TA | 36 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0091others(33): Show | 36 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.1063-7016dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138879171 | |||||
| chr5:138879171
|
T | TAA | 32 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(29): Show | 32 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1063-7017_1063-701 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138879171 | |||||
| chr5:138879171
|
T | TAAA | 18 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0017others(15): Show | 18 | HG01099.hp2 HG01109.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.1063-7018_1063-701 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138879171 | |||||
| chr5:138879171
|
T | TAAAA | 26 | a0001c0002t0002g0003a0001c0002t0002g0035a0001c0002t0002g0051others(23): Show | 26 | HG00642.hp1 HG00741.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.1063-7019_1063-701 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138879171 | |||||
| chr5:138879171
|
T | TAAAAA | 9 | a0001c0002t0002g0002a0001c0002t0002g0056a0001c0002t0002g0058others(6): Show | 9 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1063-7020_1063-701 others(9): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138879171 | |||||
| chr5:138879172
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1063-7040A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138879172 | ||||||
| chr5:138879473
|
G | GT | 6 | a0001c0001t0001g0088a0001c0001t0001g0101a0001c0001t0001g0176others(3): Show | 6 | HG01099.hp2 HG01891.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1063-6730dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138879473 | |||||
| chr5:138879482
|
T | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-6730T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138879482 | ||||||
| chr5:138879631
|
T | A | 1 | a0001c0005t0001g0156 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1063-6581T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138879631 | ||||||
| chr5:138879639
|
G | A | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1063-6573G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138879639 | ||||||
| chr5:138879720
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1063-6492A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138879720 | ||||||
| chr5:138879794
|
G | A | 6 | a0001c0002t0003g0004a0001c0002t0003g0043a0001c0002t0003g0044others(3): Show | 6 | HG01167.hp2 HG01243.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1063-6418G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138879794 | ||||||
| chr5:138880112
|
T | C | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-6100T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138880112 | ||||||
| chr5:138880221
|
T | C | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1063-5991T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138880221 | ||||||
| chr5:138880314
|
T | A | 1 | a0001c0001t0001g0042 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1063-5898T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138880314 | ||||||
| chr5:138880377
|
T | C | 69 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(66): Show | 69 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1063-5835T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138880377 | ||||||
| chr5:138880594
|
A | G | 65 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(62): Show | 65 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1063-5618A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138880594 | ||||||
| chr5:138880723
|
A | G | 2 | a0001c0002t0002g0080a0001c0002t0002g0081 | 2 | HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1063-5489A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138880723 | ||||||
| chr5:138880763
|
A | G | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1063-5449A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138880763 | ||||||
| chr5:138880936
|
G | GA | 40 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(37): Show | 40 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1063-5265dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138880936 | |||||
| chr5:138880946
|
A | AC | 3 | a0001c0002t0005g0026a0001c0002t0005g0050a0001c0002t0005g0068 | 3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1063-5266_1063-526 others(5): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138880946 | ||||||
| chr5:138880971
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1063-5241A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138880971 | ||||||
| chr5:138881438
|
T | C | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-4774T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138881438 | ||||||
| chr5:138881468
|
T | C | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-4744T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138881468 | ||||||
| chr5:138881616
|
T | C | 36 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(33): Show | 36 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1063-4596T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138881616 | ||||||
| chr5:138881761
|
T | TTTG | 69 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(66): Show | 69 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1063-4438_1063-443 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138881761 | |||||
| chr5:138882022
|
T | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1063-4190T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138882022 | ||||||
| chr5:138882061
|
T | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1063-4151T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138882061 | ||||||
| chr5:138882077
|
C | G | 4 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063-4135C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138882077 | ||||||
| chr5:138882115
|
A | G | 2 | a0001c0001t0001g0101a0001c0002t0003g0023 | 2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1063-4097A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138882115 | ||||||
| chr5:138882134
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1063-4078T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138882134 | ||||||
| chr5:138882345
|
A | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1063-3867A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138882345 | ||||||
| chr5:138882489
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1063-3723A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138882489 | ||||||
| chr5:138882956
|
G | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-3256G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138882956 | ||||||
| chr5:138883158
|
C | T | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-3054C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138883158 | ||||||
| chr5:138883373
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp2 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-2839C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138883373 | ||||||
| chr5:138884190
|
G | A | 2 | a0001c0002t0003g0025a0001c0012t0003g0019 | 2 | HG02280.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1063-2022G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138884190 | ||||||
| chr5:138884630
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1063-1582A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138884630 | ||||||
| chr5:138884668
|
T | C | 2 | a0001c0004t0004g0005a0001c0009t0004g0006 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1063-1544T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138884668 | ||||||
| chr5:138885086
|
A | G | 13 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(10): Show | 13 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1063-1126A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138885086 | ||||||
| chr5:138885471
|
G | T | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1063-741G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138885471 | ||||||
| chr5:138885530
|
T | TA | 2 | a0001c0002t0002g0056a0001c0002t0002g0060 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1063-681dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138885530 | |||||
| chr5:138885569
|
G | A | 1 | a0001c0002t0002g0072 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1063-643G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138885569 | ||||||
| chr5:138885678
|
C | G | 1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1063-534C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138885678 | ||||||
| chr5:138885917
|
T | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | NA18946.hp2 NA19003.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1063-295T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138885917 | ||||||
| chr5:138886300
|
G | C | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
splice_region_variant&intron_variant | LOW | c.1143+8G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 8/17 | chr5 | 138886300 | ||||||
| chr5:138886641
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1143+349G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 8/17 | chr5 | 138886641 | ||||||
| chr5:138886905
|
A | G | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1144-585A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 8/17 | chr5 | 138886905 | ||||||
| chr5:138887051
|
C | G | 1 | a0001c0014t0001g0145 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1144-439C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 8/17 | chr5 | 138887051 | ||||||
| chr5:138887139
|
A | T | 1 | a0001c0001t0001g0126 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1144-351A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 8/17 | chr5 | 138887139 | ||||||
| chr5:138887191
|
G | A | 3 | a0001c0005t0001g0156a0001c0005t0001g0167a0001c0005t0001g0168 | 3 | HG00099.hp1 HG00741.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1144-299G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 8/17 | chr5 | 138887191 | ||||||
| chr5:138887305
|
C | G | 54 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(51): Show | 54 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.1144-185C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 8/17 | chr5 | 138887305 | ||||||
| chr5:138887467
|
A | T | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1144-23A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 8/17 | chr5 | 138887467 | ||||||
| chr5:138887888
|
C | T | 2 | a0001c0002t0005g0050a0001c0002t0005g0068 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1296+246C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138887888 | ||||||
| chr5:138887944
|
A | G | 64 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(61): Show | 64 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1296+302A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138887944 | ||||||
| chr5:138887983
|
C | T | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1296+341C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138887983 | ||||||
| chr5:138888103
|
A | G | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1296+461A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138888103 | ||||||
| chr5:138888359
|
A | G | 69 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(66): Show | 69 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1296+717A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138888359 | ||||||
| chr5:138888586
|
A | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(80): Show | 83 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1296+944A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138888586 | ||||||
| chr5:138888594
|
C | T | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1296+952C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138888594 | ||||||
| chr5:138888609
|
A | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(80): Show | 83 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1296+967A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138888609 | ||||||
| chr5:138888746
|
C | T | 10 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(7): Show | 10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1296+1104C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138888746 | ||||||
| chr5:138888885
|
G | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+1243G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138888885 | ||||||
| chr5:138889169
|
A | G | 1 | a0001c0003t0002g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1296+1527A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138889169 | ||||||
| chr5:138889532
|
G | A | 1 | a0001c0001t0006g0174 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1296+1890G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138889532 | ||||||
| chr5:138889905
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1296+2263C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138889905 | ||||||
| chr5:138890264
|
T | C | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+2622T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138890264 | ||||||
| chr5:138890326
|
T | G | 10 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(7): Show | 10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1296+2684T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138890326 | ||||||
| chr5:138890349
|
AT | A | 68 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(65): Show | 68 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1296+2710delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138890349 | |||||
| chr5:138890529
|
G | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1296+2887G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138890529 | ||||||
| chr5:138890576
|
A | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1296+2934A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138890576 | ||||||
| chr5:138891039
|
A | G | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+3397A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138891039 | ||||||
| chr5:138891078
|
T | C | 69 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(66): Show | 69 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1296+3436T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138891078 | ||||||
| chr5:138891376
|
A | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(80): Show | 83 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1296+3734A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138891376 | ||||||
| chr5:138891396
|
C | CT | 40 | a0001c0001t0001g0176a0001c0002t0002g0002a0001c0002t0002g0003others(37): Show | 40 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1296+3764dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138891396 | |||||
| chr5:138891578
|
G | A | 4 | a0001c0001t0001g0088a0001c0001t0001g0149a0003c0007t0001g0099others(1): Show | 4 | HG02723.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1296+3936G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138891578 | ||||||
| chr5:138891710
|
G | C | 26 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(23): Show | 26 | HG00438.hp2 HG00741.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1296+4068G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138891710 | ||||||
| chr5:138891947
|
G | A | 14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1296+4305G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138891947 | ||||||
| chr5:138892004
|
G | T | 1 | a0001c0001t0001g0040 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1296+4362G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138892004 | ||||||
| chr5:138892037
|
C | T | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1296+4395C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138892037 | ||||||
| chr5:138892090
|
T | G | 2 | a0001c0004t0004g0005a0001c0009t0004g0006 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1296+4448T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138892090 | ||||||
| chr5:138892328
|
G | GT | 28 | a0001c0001t0001g0040a0001c0001t0001g0046a0001c0001t0001g0096others(25): Show | 28 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1296+4715dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138892328 | |||||
| chr5:138892328
|
G | GTT | 16 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0128others(13): Show | 16 | HG00423.hp2 HG00438.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.1296+4714_1296+471 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138892328 | |||||
| chr5:138892328
|
G | GTTTT | 8 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0092others(5): Show | 8 | HG02895.hp2 HG03486.hp1 NA18522.hp2 others(5): Show |
intron_variant | MODIFIER | c.1296+4712_1296+471 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138892328 | |||||
| chr5:138892328
|
G | GTTTTT | 5 | a0001c0001t0001g0087a0001c0001t0001g0091a0001c0001t0001g0118others(2): Show | 5 | HG00741.hp1 HG02486.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.1296+4711_1296+471 others(9): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138892328 | |||||
| chr5:138892328
|
GT | G | 13 | a0001c0001t0001g0088a0001c0001t0001g0135a0001c0001t0001g0171others(10): Show | 13 | HG01071.hp2 HG01361.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.1296+4715delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138892328 | |||||
| chr5:138892328
|
GTT | G | 6 | a0001c0002t0003g0020a0001c0002t0003g0029a0001c0002t0005g0026others(3): Show | 6 | HG02647.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1296+4714_1296+471 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138892328 | |||||
| chr5:138892328
|
GTTTTTTT | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(7): Show | 10 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1296+4709_1296+471 others(11): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138892328 | |||||
| chr5:138892328
|
GTTTTTTT others(3): Show |
G | 34 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(31): Show | 34 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1296+4706_1296+471 others(14): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138892328 | |||||
| chr5:138892328
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0002t0002g0060 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1296+4705_1296+471 others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138892328 | |||||
| chr5:138892939
|
C | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+5297C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138892939 | ||||||
| chr5:138892973
|
G | A | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1296+5331G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138892973 | ||||||
| chr5:138893159
|
G | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+5517G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138893159 | ||||||
| chr5:138893282
|
C | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+5640C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138893282 | ||||||
| chr5:138893357
|
G | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+5715G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138893357 | ||||||
| chr5:138893515
|
A | G | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1296+5873A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138893515 | ||||||
| chr5:138893595
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1296+5953T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138893595 | ||||||
| chr5:138893632
|
G | A | 69 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(66): Show | 69 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1296+5990G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138893632 | ||||||
| chr5:138893793
|
T | G | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+6151T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138893793 | ||||||
| chr5:138893843
|
C | T | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1296+6201C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138893843 | ||||||
| chr5:138893865
|
T | G | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+6223T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138893865 | ||||||
| chr5:138894275
|
C | CTTTCTT | 37 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(34): Show | 37 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1296+6638_1296+663 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138894275 | |||||
| chr5:138894279
|
C | CTTTT | 36 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(33): Show | 36 | HG00438.hp2 HG00741.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.1296+6638_1296+663 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138894279 | |||||
| chr5:138894280
|
T | TTTTTC | 4 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1296+6638_1296+663 others(9): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138894280 | ||||||
| chr5:138894281
|
C | T | 48 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175others(45): Show | 48 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1296+6639C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138894281 | ||||||
| chr5:138894281
|
CT | C | 5 | a0001c0001t0001g0109a0001c0001t0001g0115a0001c0001t0001g0158others(2): Show | 5 | HG01070.hp1 HG01099.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1296+6657delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138894281 | |||||
| chr5:138894284
|
T | TCTTTC | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1296+6642_1296+664 others(9): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138894284 | ||||||
| chr5:138894442
|
A | G | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+6800A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138894442 | ||||||
| chr5:138894574
|
A | G | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1296+6932A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138894574 | ||||||
| chr5:138894595
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1296+6953C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138894595 | ||||||
| chr5:138894641
|
C | CTGATTA | 7 | a0001c0001t0001g0152a0001c0001t0001g0155a0001c0002t0002g0054others(4): Show | 7 | HG00423.hp2 HG01433.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1296+7035_1296+704 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138894641 | |||||
| chr5:138894641
|
CTGATTA | C | 11 | a0001c0001t0001g0036a0001c0001t0001g0103a0001c0001t0001g0151others(8): Show | 11 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1296+7035_1296+704 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138894641 | |||||
| chr5:138894641
|
CTGATTAT others(5): Show |
C | 12 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(9): Show | 12 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1296+7029_1296+704 others(16): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138894641 | |||||
| chr5:138894753
|
T | G | 1 | a0001c0002t0003g0024 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1296+7111T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138894753 | ||||||
| chr5:138894939
|
C | T | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1296+7297C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138894939 | ||||||
| chr5:138894962
|
T | C | 3 | a0001c0002t0002g0053a0001c0002t0002g0054a0001c0002t0002g0072 | 3 | HG01433.hp2 HG01515.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1296+7320T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138894962 | ||||||
| chr5:138895269
|
A | G | 1 | a0001c0002t0002g0074 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1296+7627A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138895269 | ||||||
| chr5:138895416
|
G | A | 2 | a0001c0002t0005g0050a0001c0002t0005g0068 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1296+7774G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138895416 | ||||||
| chr5:138895503
|
TG | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 84 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.1296+7871delG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138895503 | |||||
| chr5:138895714
|
C | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(94): Show | 97 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1296+8072C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138895714 | ||||||
| chr5:138895956
|
C | T | 69 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(66): Show | 69 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1296+8314C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138895956 | ||||||
| chr5:138896266
|
T | G | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1297-8083T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138896266 | ||||||
| chr5:138896389
|
T | C | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0165 | 3 | HG02970.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1297-7960T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138896389 | ||||||
| chr5:138896398
|
T | C | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1297-7951T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138896398 | ||||||
| chr5:138896545
|
T | C | 4 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1297-7804T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138896545 | ||||||
| chr5:138896736
|
A | G | 3 | a0001c0002t0003g0029a0001c0002t0008g0028a0001c0013t0003g0031 | 3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1297-7613A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138896736 | ||||||
| chr5:138896838
|
G | A | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1297-7511G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138896838 | ||||||
| chr5:138897050
|
A | G | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-7299A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897050 | ||||||
| chr5:138897084
|
G | GC | 107 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(104): Show | 107 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1297-7265_1297-726 others(5): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897084 | ||||||
| chr5:138897294
|
A | AC | 37 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(34): Show | 37 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1297-7041dupC | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138897294 | |||||
| chr5:138897294
|
A | ACC | 28 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(25): Show | 28 | HG01071.hp2 HG01074.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.1297-7042_1297-704 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138897294 | |||||
| chr5:138897294
|
A | ACCC | 14 | a0001c0001t0001g0017a0001c0001t0001g0037a0001c0001t0001g0092others(11): Show | 14 | HG00323.hp1 HG00438.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1297-7043_1297-704 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138897294 | |||||
| chr5:138897294
|
AC | A | 19 | a0001c0001t0001g0087a0001c0001t0001g0101a0001c0001t0001g0102others(16): Show | 19 | HG01099.hp2 HG01109.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.1297-7041delC | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138897294 | |||||
| chr5:138897294
|
ACCCCCCC others(4): Show |
A | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1297-7051_1297-704 others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138897294 | |||||
| chr5:138897297
|
C | G | 1 | a0001c0002t0003g0021 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1297-7052C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897297 | ||||||
| chr5:138897298
|
C | G | 3 | a0001c0002t0003g0022a0001c0002t0003g0023a0001c0002t0003g0024 | 3 | HG01109.hp2 HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1297-7051C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897298 | ||||||
| chr5:138897303
|
C | G | 1 | a0001c0001t0001g0087 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1297-7046C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897303 | ||||||
| chr5:138897309
|
G | C | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-7040G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897309 | ||||||
| chr5:138897310
|
C | G | 10 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(7): Show | 10 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1297-7039C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897310 | ||||||
| chr5:138897497
|
A | G | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-6852A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897497 | ||||||
| chr5:138897683
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1297-6666C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897683 | ||||||
| chr5:138897892
|
C | G | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-6457C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897892 | ||||||
| chr5:138897965
|
A | G | 1 | a0001c0002t0002g0082 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1297-6384A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897965 | ||||||
| chr5:138898158
|
A | AC | 56 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(53): Show | 56 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.1297-6182dupC | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138898158 | |||||
| chr5:138898194
|
C | A | 1 | a0001c0001t0001g0039 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1297-6155C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138898194 | ||||||
| chr5:138898308
|
A | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1297-6041A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138898308 | ||||||
| chr5:138898427
|
G | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(98): Show | 101 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1297-5922G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138898427 | ||||||
| chr5:138898441
|
G | T | 65 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(62): Show | 65 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1297-5908G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138898441 | ||||||
| chr5:138898601
|
T | TA | 62 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(59): Show | 62 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.1297-5732dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138898601 | |||||
| chr5:138898601
|
T | TAA | 7 | a0001c0001t0001g0088a0001c0001t0001g0149a0001c0002t0002g0082others(4): Show | 7 | HG02486.hp2 HG02602.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1297-5733_1297-573 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138898601 | |||||
| chr5:138899160
|
G | A | 3 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023 | 3 | HG01993.hp1 HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1297-5189G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138899160 | ||||||
| chr5:138899184
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1297-5165C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138899184 | ||||||
| chr5:138899348
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1297-5001C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138899348 | ||||||
| chr5:138899688
|
C | A | 1 | a0001c0003t0002g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1297-4661C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138899688 | ||||||
| chr5:138899851
|
A | G | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1297-4498A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138899851 | ||||||
| chr5:138900011
|
T | G | 3 | a0001c0002t0005g0026a0001c0002t0005g0050a0001c0002t0005g0068 | 3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1297-4338T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138900011 | ||||||
| chr5:138900307
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1297-4042A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138900307 | ||||||
| chr5:138900379
|
TTATGAGA others(2029): Show |
T | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1297-3968_1297-193 others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138900379 | |||||
| chr5:138900631
|
A | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1297-3718A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138900631 | ||||||
| chr5:138901029
|
C | G | 3 | a0001c0002t0005g0026a0001c0002t0005g0050a0001c0002t0005g0068 | 3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1297-3320C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901029 | ||||||
| chr5:138901066
|
G | A | 64 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(61): Show | 64 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1297-3283G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901066 | ||||||
| chr5:138901140
|
C | T | 1 | a0001c0002t0002g0054 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1297-3209C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901140 | ||||||
| chr5:138901218
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1297-3131C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901218 | ||||||
| chr5:138901252
|
A | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(103): Show | 106 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.1297-3097A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901252 | ||||||
| chr5:138901262
|
A | G | 3 | a0001c0002t0003g0029a0001c0002t0008g0028a0001c0013t0003g0031 | 3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1297-3087A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901262 | ||||||
| chr5:138901572
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1297-2777G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901572 | ||||||
| chr5:138901591
|
A | G | 1 | a0001c0002t0005g0050 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1297-2758A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901591 | ||||||
| chr5:138901604
|
T | G | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-2745T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901604 | ||||||
| chr5:138901613
|
G | C | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1297-2736G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901613 | ||||||
| chr5:138901727
|
C | T | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-2622C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901727 | ||||||
| chr5:138901868
|
A | G | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1297-2481A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901868 | ||||||
| chr5:138901944
|
G | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1297-2405G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901944 | ||||||
| chr5:138902069
|
A | T | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-2280A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902069 | ||||||
| chr5:138902354
|
G | A | 68 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(65): Show | 68 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1297-1995G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902354 | ||||||
| chr5:138902419
|
G | T | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1297-1930G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902419 | ||||||
| chr5:138902426
|
G | T | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1297-1923G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902426 | ||||||
| chr5:138902432
|
G | T | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1297-1917G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902432 | ||||||
| chr5:138902482
|
T | G | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1297-1867T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902482 | ||||||
| chr5:138902511
|
T | C | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1297-1838T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902511 | ||||||
| chr5:138902513
|
A | G | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1297-1836A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902513 | ||||||
| chr5:138902565
|
G | A | 10 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(7): Show | 10 | HG00423.hp1 NA18946.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.1297-1784G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902565 | ||||||
| chr5:138902602
|
G | C | 1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1297-1747G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902602 | ||||||
| chr5:138902630
|
A | G | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1297-1719A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902630 | ||||||
| chr5:138902641
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1297-1708G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902641 | ||||||
| chr5:138902719
|
C | T | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-1630C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902719 | ||||||
| chr5:138902736
|
A | G | 3 | a0001c0002t0005g0026a0001c0002t0005g0050a0001c0002t0005g0068 | 3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1297-1613A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902736 | ||||||
| chr5:138902854
|
A | G | 6 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0114others(3): Show | 6 | HG02132.hp2 HG02602.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1297-1495A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902854 | ||||||
| chr5:138903049
|
T | G | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1297-1300T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138903049 | ||||||
| chr5:138903113
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1297-1236A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138903113 | ||||||
| chr5:138903116
|
T | G | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1297-1233T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138903116 | ||||||
| chr5:138903118
|
T | C | 5 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 5 | HG01070.hp1 HG01109.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1297-1231T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138903118 | ||||||
| chr5:138903158
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1297-1191C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138903158 | ||||||
| chr5:138903249
|
C | T | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1297-1100C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138903249 | ||||||
| chr5:138903663
|
C | T | 1 | a0001c0002t0002g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1297-686C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138903663 | ||||||
| chr5:138903989
|
C | T | 1 | a0001c0002t0003g0029 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1297-360C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138903989 | ||||||
| chr5:138904224
|
G | A | 1 | a0001c0002t0002g0080 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1297-125G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138904224 | ||||||
| chr5:138904235
|
C | G | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-114C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138904235 | ||||||
| chr5:138904704
|
C | T | 2 | a0001c0004t0004g0005a0001c0009t0004g0006 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1389+263C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138904704 | ||||||
| chr5:138904833
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1389+392G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138904833 | ||||||
| chr5:138905018
|
T | C | 69 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(66): Show | 69 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1389+577T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138905018 | ||||||
| chr5:138905028
|
A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0123 | 2 | HG00099.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1389+587A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138905028 | ||||||
| chr5:138905049
|
G | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1389+608G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138905049 | ||||||
| chr5:138905093
|
C | CA | 14 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(11): Show | 14 | HG00423.hp2 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1389+671dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138905093 | |||||
| chr5:138905093
|
C | CAA | 6 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1389+670_1389+671d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138905093 | |||||
| chr5:138905111
|
A | AAAATACA others(7): Show |
1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1389+671_1389+672i others(16): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138905111 | |||||
| chr5:138905111
|
A | AAATACAT others(6): Show |
14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0046others(11): Show | 14 | HG00438.hp2 HG01167.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1389+671_1389+672i others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138905111 | |||||
| chr5:138905111
|
A | AAATACAT others(10): Show |
5 | a0001c0002t0008g0028a0001c0004t0004g0005a0001c0004t0004g0180others(2): Show | 5 | HG02486.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1389+671_1389+672i others(19): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138905111 | |||||
| chr5:138905111
|
A | AATACATA others(5): Show |
46 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0002t0002g0002others(43): Show | 46 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.1389+678_1389+689d others(14): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138905111 | |||||
| chr5:138905111
|
A | AATACATA others(9): Show |
2 | a0001c0002t0003g0029a0001c0002t0005g0050 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1389+674_1389+689d others(18): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138905111 | |||||
| chr5:138905111
|
A | ACATACAT others(10): Show |
1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1389+670_1389+671i others(19): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138905111 | ||||||
| chr5:138905185
|
G | T | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1389+744G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138905185 | ||||||
| chr5:138905243
|
T | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1389+802T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138905243 | ||||||
| chr5:138905550
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1389+1109A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138905550 | ||||||
| chr5:138905586
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1389+1145C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138905586 | ||||||
| chr5:138905629
|
A | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 84 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.1389+1188A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138905629 | ||||||
| chr5:138905824
|
C | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1389+1383C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138905824 | ||||||
| chr5:138906076
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1389+1635G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138906076 | ||||||
| chr5:138906131
|
C | G | 65 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(62): Show | 65 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1389+1690C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138906131 | ||||||
| chr5:138906309
|
A | G | 1 | a0004c0010t0001g0169 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1389+1868A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138906309 | ||||||
| chr5:138906840
|
T | C | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1389+2399T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138906840 | ||||||
| chr5:138907211
|
G | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1389+2770G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138907211 | ||||||
| chr5:138907409
|
G | A | 69 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(66): Show | 69 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1389+2968G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138907409 | ||||||
| chr5:138907468
|
C | T | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1389+3027C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138907468 | ||||||
| chr5:138907470
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1389+3029G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138907470 | ||||||
| chr5:138907481
|
G | C | 1 | a0001c0002t0005g0068 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1389+3040G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138907481 | ||||||
| chr5:138907523
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1389+3082C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138907523 | ||||||
| chr5:138907577
|
G | A | 7 | a0001c0001t0001g0094a0001c0001t0001g0108a0001c0001t0001g0109others(4): Show | 7 | HG00423.hp2 HG02132.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1389+3136G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138907577 | ||||||
| chr5:138907739
|
T | C | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1389+3298T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138907739 | ||||||
| chr5:138907924
|
G | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1389+3483G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138907924 | ||||||
| chr5:138907965
|
C | T | 2 | a0001c0003t0002g0062a0001c0003t0002g0064 | 2 | HG01346.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1389+3524C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138907965 | ||||||
| chr5:138907969
|
C | CTT | 19 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(16): Show | 19 | HG00438.hp2 HG00741.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1389+3537_1389+353 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138907969 | |||||
| chr5:138908130
|
A | T | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1389+3689A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138908130 | ||||||
| chr5:138908342
|
C | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1389+3901C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138908342 | ||||||
| chr5:138908579
|
C | CGCTTGAG others(12): Show |
4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1389+4153_1389+415 others(23): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138908579 | |||||
| chr5:138908579
|
C | T | 85 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1389+4138C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138908579 | ||||||
| chr5:138908587
|
C | T | 3 | a0001c0002t0003g0020a0001c0002t0003g0025a0001c0012t0003g0019 | 3 | HG02280.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1389+4146C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138908587 | ||||||
| chr5:138908703
|
A | T | 1 | a0001c0001t0001g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1389+4262A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138908703 | ||||||
| chr5:138908773
|
AAG | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | NA18946.hp2 NA19003.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1389+4335_1389+433 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138908773 | |||||
| chr5:138909033
|
C | A | 1 | a0001c0002t0002g0053 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1389+4592C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138909033 | ||||||
| chr5:138909234
|
A | C | 1 | a0001c0001t0001g0172 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1389+4793A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138909234 | ||||||
| chr5:138909359
|
C | G | 5 | a0001c0002t0003g0004a0001c0002t0003g0043a0001c0002t0003g0044others(2): Show | 5 | HG01243.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1389+4918C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138909359 | ||||||
| chr5:138909462
|
A | C | 1 | a0001c0001t0001g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1389+5021A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138909462 | ||||||
| chr5:138909531
|
A | T | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1389+5090A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138909531 | ||||||
| chr5:138909720
|
G | T | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1389+5279G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138909720 | ||||||
| chr5:138909740
|
T | G | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1389+5299T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138909740 | ||||||
| chr5:138910226
|
C | CT | 6 | a0001c0001t0001g0097a0001c0001t0001g0134a0001c0001t0001g0147others(3): Show | 6 | HG00438.hp1 HG01099.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1389+5812dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138910226 | |||||
| chr5:138910226
|
CT | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0013others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.1389+5812delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138910226 | |||||
| chr5:138910226
|
CTT | C | 41 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(38): Show | 41 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1389+5811_1389+581 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138910226 | |||||
| chr5:138910226
|
CTTT | C | 7 | a0001c0001t0001g0124a0001c0002t0002g0003a0001c0002t0002g0053others(4): Show | 7 | HG01433.hp1 HG01515.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1389+5810_1389+581 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138910226 | |||||
| chr5:138910226
|
CTTTT | C | 10 | a0001c0002t0003g0004a0001c0002t0003g0020a0001c0002t0003g0025others(7): Show | 10 | HG00741.hp1 HG01243.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1389+5809_1389+581 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138910226 | |||||
| chr5:138910226
|
CTTTTT | C | 6 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(3): Show | 6 | HG01109.hp2 HG01167.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1389+5808_1389+581 others(9): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138910226 | |||||
| chr5:138910226
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0004t0004g0005a0001c0012t0003g0019 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1389+5802_1389+581 others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138910226 | |||||
| chr5:138910252
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1389+5811T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138910252 | ||||||
| chr5:138910412
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1389+5971G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138910412 | ||||||
| chr5:138910472
|
G | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1389+6031G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138910472 | ||||||
| chr5:138910542
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1389+6101C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138910542 | ||||||
| chr5:138910639
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 79 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.1389+6198G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138910639 | ||||||
| chr5:138910787
|
A | G | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1389+6346A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138910787 | ||||||
| chr5:138911089
|
T | C | 60 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(57): Show | 60 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1389+6648T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138911089 | ||||||
| chr5:138911376
|
C | T | 4 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1390-6366C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138911376 | ||||||
| chr5:138911458
|
A | AC | 17 | a0001c0002t0002g0075a0001c0002t0002g0084a0001c0002t0003g0004others(14): Show | 17 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1390-6275dupC | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138911458 | |||||
| chr5:138911459
|
C | T | 2 | a0001c0001t0006g0174a0001c0001t0006g0175 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1390-6283C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138911459 | ||||||
| chr5:138911515
|
G | T | 1 | a0001c0002t0002g0059 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1390-6227G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138911515 | ||||||
| chr5:138911891
|
A | G | 3 | a0001c0002t0005g0026a0001c0002t0005g0050a0001c0002t0005g0068 | 3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1390-5851A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138911891 | ||||||
| chr5:138911948
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1390-5794C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138911948 | ||||||
| chr5:138912226
|
G | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1390-5516G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138912226 | ||||||
| chr5:138912338
|
G | T | 4 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1390-5404G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138912338 | ||||||
| chr5:138912376
|
TAGA | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1390-5359_1390-535 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138912376 | |||||
| chr5:138912699
|
C | T | 4 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1390-5043C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138912699 | ||||||
| chr5:138912758
|
TTA | T | 64 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(61): Show | 64 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1390-4979_1390-497 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138912758 | |||||
| chr5:138912885
|
T | A | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1390-4857T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138912885 | ||||||
| chr5:138912885
|
T | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0018 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1390-4857T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138912885 | ||||||
| chr5:138912965
|
C | T | 3 | a0001c0002t0005g0026a0001c0002t0005g0050a0001c0002t0005g0068 | 3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1390-4777C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138912965 | ||||||
| chr5:138913054
|
G | A | 1 | a0001c0011t0001g0107 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1390-4688G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138913054 | ||||||
| chr5:138913058
|
CT | C | 18 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(15): Show | 18 | HG02257.hp1 HG02451.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1390-4672delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138913058 | |||||
| chr5:138913058
|
CTT | C | 60 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(57): Show | 60 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1390-4673_1390-467 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138913058 | |||||
| chr5:138913076
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1390-4666T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138913076 | ||||||
| chr5:138913316
|
G | T | 9 | a0001c0002t0003g0004a0001c0002t0003g0032a0001c0002t0003g0033others(6): Show | 9 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1390-4426G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138913316 | ||||||
| chr5:138913569
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0123 | 2 | HG00099.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1390-4173G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138913569 | ||||||
| chr5:138913583
|
CA | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 76 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.1390-4143delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138913583 | |||||
| chr5:138913670
|
G | T | 1 | a0001c0001t0001g0161 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1390-4072G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138913670 | ||||||
| chr5:138913860
|
A | G | 10 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(7): Show | 10 | HG00423.hp1 NA18946.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.1390-3882A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138913860 | ||||||
| chr5:138913887
|
G | T | 8 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0114others(5): Show | 8 | HG02132.hp2 HG02602.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1390-3855G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138913887 | ||||||
| chr5:138913892
|
T | C | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0161 | 3 | HG01070.hp1 HG01109.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1390-3850T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138913892 | ||||||
| chr5:138913895
|
G | T | 9 | a0001c0001t0001g0131a0001c0001t0001g0136a0001c0001t0001g0140others(6): Show | 9 | HG02258.hp2 HG02451.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1390-3847G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138913895 | ||||||
| chr5:138913996
|
G | T | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1390-3746G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138913996 | ||||||
| chr5:138914251
|
C | A | 64 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(61): Show | 64 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1390-3491C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138914251 | ||||||
| chr5:138914417
|
G | A | 64 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(61): Show | 64 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1390-3325G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138914417 | ||||||
| chr5:138914630
|
G | A | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1390-3112G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138914630 | ||||||
| chr5:138914932
|
G | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1390-2810G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138914932 | ||||||
| chr5:138915104
|
G | A | 7 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(4): Show | 7 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1390-2638G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138915104 | ||||||
| chr5:138915235
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1390-2507C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138915235 | ||||||
| chr5:138915407
|
T | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0166a0001c0001t0001g0170 | 3 | HG00323.hp2 HG02129.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1390-2335T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138915407 | ||||||
| chr5:138915516
|
G | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1390-2226G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138915516 | ||||||
| chr5:138915587
|
A | C | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1390-2155A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138915587 | ||||||
| chr5:138915634
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1390-2108T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138915634 | ||||||
| chr5:138916000
|
G | A | 60 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(57): Show | 60 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1390-1742G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138916000 | ||||||
| chr5:138916003
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1390-1739C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138916003 | ||||||
| chr5:138916067
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1390-1675A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138916067 | ||||||
| chr5:138916177
|
C | CAAA | 5 | a0001c0001t0001g0101a0001c0002t0003g0021a0001c0002t0003g0022others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1390-1553_1390-155 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | |||||
| chr5:138916177
|
C | CAAAAAAA others(2): Show |
30 | a0001c0002t0002g0003a0001c0002t0002g0035a0001c0002t0002g0053others(27): Show | 30 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1390-1559_1390-155 others(13): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | |||||
| chr5:138916177
|
C | CAAAAAAA others(3): Show |
17 | a0001c0002t0002g0002a0001c0002t0002g0051a0001c0002t0002g0054others(14): Show | 17 | HG00741.hp1 HG01081.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1390-1560_1390-155 others(14): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | |||||
| chr5:138916177
|
C | CAAAAAAA others(4): Show |
2 | a0001c0002t0003g0047a0001c0002t0005g0050 | 2 | HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1390-1561_1390-155 others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | |||||
| chr5:138916177
|
C | CAAAAAAA others(6): Show |
3 | a0001c0002t0003g0020a0001c0002t0003g0029a0001c0013t0003g0031 | 3 | HG02723.hp1 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1390-1563_1390-155 others(17): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | |||||
| chr5:138916177
|
C | CAAAAAAA others(7): Show |
9 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(6): Show | 9 | HG02451.hp2 HG02559.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.1390-1564_1390-155 others(18): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | |||||
| chr5:138916177
|
C | CAAAAAAA others(8): Show |
4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(1): Show | 4 | HG02257.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1390-1551_1390-155 others(19): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | |||||
| chr5:138916177
|
C | CAAAAAAA others(9): Show |
1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1390-1551_1390-155 others(20): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | |||||
| chr5:138916177
|
C | CAAAAAAA others(12): Show |
1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1390-1551_1390-155 others(23): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | |||||
| chr5:138916177
|
C | CAAAAAAA others(13): Show |
1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1390-1551_1390-155 others(24): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | |||||
| chr5:138916177
|
C | CAAAAAAA others(19): Show |
2 | a0001c0001t0001g0092a0003c0007t0001g0100 | 2 | HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1390-1551_1390-155 others(30): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | |||||
| chr5:138916177
|
C | CAAAAAAA others(20): Show |
1 | a0003c0007t0001g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1390-1551_1390-155 others(31): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | |||||
| chr5:138916177
|
C | CAAAAAAA others(22): Show |
2 | a0001c0001t0001g0104a0002c0006t0001g0095 | 2 | HG00423.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1390-1551_1390-155 others(33): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | |||||
| chr5:138916177
|
C | CAAAAAAA others(25): Show |
1 | a0002c0006t0001g0090 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1390-1551_1390-155 others(36): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | |||||
| chr5:138916177
|
C | CAAAAAAA others(29): Show |
4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0093others(1): Show | 4 | HG02723.hp2 HG06807.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1390-1551_1390-155 others(40): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | |||||
| chr5:138916177
|
C | CAAAAAAA others(30): Show |
2 | a0001c0001t0001g0087a0001c0001t0001g0179 | 2 | NA18986.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1390-1551_1390-155 others(41): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | |||||
| chr5:138916177
|
C | CAAAAAAA others(31): Show |
1 | a0001c0001t0001g0118 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1390-1551_1390-155 others(42): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | |||||
| chr5:138916177
|
C | CAAAAAAA others(33): Show |
1 | a0001c0001t0001g0091 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1390-1551_1390-155 others(44): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | |||||
| chr5:138916177
|
C | CAAAAAAA others(34): Show |
1 | a0001c0001t0001g0086 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1390-1551_1390-155 others(45): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | |||||
| chr5:138916177
|
C | CAAAAAAA others(42): Show |
1 | a0001c0001t0001g0097 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1390-1551_1390-155 others(53): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | |||||
| chr5:138916312
|
C | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1390-1430C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138916312 | ||||||
| chr5:138916395
|
C | CT | 18 | a0001c0001t0001g0101a0001c0001t0001g0176a0001c0001t0006g0174others(15): Show | 18 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1390-1332dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916395 | |||||
| chr5:138916779
|
A | AT | 51 | a0001c0001t0001g0094a0001c0001t0001g0151a0001c0001t0001g0162others(48): Show | 51 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1390-953dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916779 | |||||
| chr5:138916779
|
A | ATT | 13 | a0001c0002t0003g0004a0001c0002t0003g0021a0001c0002t0003g0022others(10): Show | 13 | HG00741.hp1 HG01109.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1390-954_1390-953d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916779 | |||||
| chr5:138916782
|
T | TA | 3 | a0001c0002t0003g0020a0001c0002t0003g0025a0001c0012t0003g0019 | 3 | HG02280.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1390-960_1390-959i others(3): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138916782 | ||||||
| chr5:138916783
|
T | A | 7 | a0001c0001t0001g0088a0001c0001t0001g0149a0001c0001t0001g0176others(4): Show | 7 | HG01099.hp2 HG02723.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1390-959T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138916783 | ||||||
| chr5:138916797
|
C | G | 1 | a0001c0003t0002g0077 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1390-945C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138916797 | ||||||
| chr5:138916961
|
A | T | 1 | a0001c0001t0001g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1390-781A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138916961 | ||||||
| chr5:138916962
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1390-780C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138916962 | ||||||
| chr5:138916982
|
C | CA | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1390-759dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916982 | |||||
| chr5:138917052
|
C | T | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1390-690C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138917052 | ||||||
| chr5:138917454
|
A | C | 3 | a0001c0001t0001g0176a0001c0001t0006g0174a0001c0001t0006g0175 | 3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1390-288A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138917454 | ||||||
| chr5:138917531
|
TTTTA | T | 36 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(33): Show | 36 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1390-207_1390-204d others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138917531 | |||||
| chr5:138917731
|
A | G | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1390-11A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138917731 | ||||||
| chr5:138917982
|
A | G | 9 | a0001c0001t0001g0106a0001c0001t0001g0113a0001c0001t0001g0119others(6): Show | 9 | HG01099.hp1 HG01168.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546+84A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138917982 | ||||||
| chr5:138918194
|
G | GA | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1546+297dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138918194 | |||||
| chr5:138918456
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1546+558A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138918456 | ||||||
| chr5:138918568
|
G | A | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1546+670G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138918568 | ||||||
| chr5:138918635
|
G | C | 4 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0023others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1546+737G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138918635 | ||||||
| chr5:138918858
|
G | A | 8 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(5): Show | 8 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1546+960G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138918858 | ||||||
| chr5:138919243
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1546+1345A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138919243 | ||||||
| chr5:138919410
|
CA | C | 2 | a0001c0001t0006g0174a0001c0001t0006g0175 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1546+1513delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138919410 | ||||||
| chr5:138919857
|
G | A | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1546+1959G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138919857 | ||||||
| chr5:138919967
|
A | AT | 10 | a0001c0001t0001g0018a0001c0001t0001g0176a0001c0002t0002g0059others(7): Show | 10 | HG01074.hp1 HG01099.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1546+2095dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138919967 | |||||
| chr5:138919967
|
AT | A | 102 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1546+2095delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138919967 | |||||
| chr5:138919967
|
ATT | A | 5 | a0001c0001t0001g0115a0001c0001t0001g0141a0001c0001t0001g0153others(2): Show | 5 | HG01074.hp2 HG01515.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546+2094_1546+209 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138919967 | |||||
| chr5:138919967
|
ATTT | A | 9 | a0001c0002t0003g0004a0001c0002t0003g0032a0001c0002t0003g0033others(6): Show | 9 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546+2093_1546+209 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138919967 | |||||
| chr5:138920040
|
G | A | 9 | a0001c0002t0003g0004a0001c0002t0003g0032a0001c0002t0003g0033others(6): Show | 9 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546+2142G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920040 | ||||||
| chr5:138920272
|
G | C | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1546+2374G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920272 | ||||||
| chr5:138920279
|
C | G | 2 | a0001c0001t0006g0174a0001c0001t0006g0175 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1546+2381C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920279 | ||||||
| chr5:138920329
|
T | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(75): Show | 78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.1546+2431T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920329 | ||||||
| chr5:138920410
|
G | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 76 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.1546+2512G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920410 | ||||||
| chr5:138920450
|
C | T | 36 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(33): Show | 36 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1546+2552C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920450 | ||||||
| chr5:138920497
|
G | T | 1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1546+2599G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920497 | ||||||
| chr5:138920589
|
C | T | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1546+2691C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920589 | ||||||
| chr5:138920608
|
T | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1546+2710T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920608 | ||||||
| chr5:138920616
|
A | G | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1546+2718A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920616 | ||||||
| chr5:138920964
|
A | T | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1546+3066A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920964 | ||||||
| chr5:138921596
|
A | AT | 20 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(17): Show | 20 | HG00323.hp2 HG01891.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.1547-2891dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138921596 | |||||
| chr5:138921596
|
A | ATT | 7 | a0001c0001t0001g0018a0001c0002t0002g0003a0001c0002t0002g0061others(4): Show | 7 | HG01975.hp1 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1547-2892_1547-289 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138921596 | |||||
| chr5:138921596
|
A | ATTT | 40 | a0001c0002t0002g0035a0001c0002t0002g0051a0001c0002t0002g0053others(37): Show | 40 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1547-2893_1547-289 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138921596 | |||||
| chr5:138921596
|
A | ATTTT | 5 | a0001c0002t0002g0002a0001c0002t0002g0058a0001c0002t0002g0072others(2): Show | 5 | HG01981.hp1 HG02258.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1547-2894_1547-289 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138921596 | |||||
| chr5:138921596
|
A | ATTTTT | 22 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(19): Show | 22 | HG00423.hp1 HG01109.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.1547-2895_1547-289 others(9): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138921596 | |||||
| chr5:138921821
|
G | A | 1 | a0001c0002t0003g0021 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1547-2689G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138921821 | ||||||
| chr5:138921907
|
C | G | 1 | a0001c0002t0002g0079 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1547-2603C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138921907 | ||||||
| chr5:138921907
|
C | T | 1 | a0001c0002t0002g0073 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1547-2603C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138921907 | ||||||
| chr5:138921917
|
A | AT | 12 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(9): Show | 12 | HG00423.hp1 HG02258.hp2 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1547-2580dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138921917 | |||||
| chr5:138922163
|
C | G | 4 | a0001c0001t0001g0113a0001c0001t0001g0119a0001c0001t0001g0120others(1): Show | 4 | HG01433.hp1 HG01975.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-2347C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138922163 | ||||||
| chr5:138922181
|
A | T | 1 | a0001c0002t0002g0079 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1547-2329A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138922181 | ||||||
| chr5:138922220
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.1547-2290T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138922220 | ||||||
| chr5:138922488
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(87): Show | 90 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.1547-2022G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138922488 | ||||||
| chr5:138922664
|
C | T | 2 | a0001c0001t0007g0111a0001c0001t0007g0112 | 2 | HG01099.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.1547-1846C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138922664 | ||||||
| chr5:138922672
|
C | A | 9 | a0001c0002t0003g0004a0001c0002t0003g0032a0001c0002t0003g0033others(6): Show | 9 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1547-1838C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138922672 | ||||||
| chr5:138922672
|
C | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0149 | 2 | HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1547-1838C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138922672 | ||||||
| chr5:138922894
|
G | A | 2 | a0001c0001t0006g0174a0001c0001t0006g0175 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1547-1616G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138922894 | ||||||
| chr5:138922930
|
TA | T | 53 | a0001c0001t0006g0174a0001c0001t0006g0175a0001c0002t0002g0002others(50): Show | 53 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1547-1566delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138922930 | |||||
| chr5:138922947
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1547-1563G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138922947 | ||||||
| chr5:138923001
|
T | TGTTTAA | 76 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(73): Show | 76 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1547-1509_1547-150 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138923001 | ||||||
| chr5:138923061
|
A | G | 2 | a0001c0002t0002g0080a0001c0002t0002g0081 | 2 | HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1547-1449A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138923061 | ||||||
| chr5:138923113
|
A | C | 76 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(73): Show | 76 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1547-1397A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138923113 | ||||||
| chr5:138923636
|
C | T | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-874C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138923636 | ||||||
| chr5:138923754
|
C | T | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1547-756C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138923754 | ||||||
| chr5:138923853
|
T | A | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1547-657T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138923853 | ||||||
| chr5:138923953
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1547-557G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138923953 | ||||||
| chr5:138924149
|
T | TA | 2 | a0001c0001t0006g0174a0001c0001t0006g0175 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1547-360dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138924149 | |||||
| chr5:138924282
|
G | GT | 46 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(43): Show | 46 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.1547-215dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138924282 | |||||
| chr5:138924282
|
G | T | 1 | a0001c0002t0002g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1547-228G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138924282 | ||||||
| chr5:138924295
|
TA | T | 18 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(15): Show | 18 | HG02257.hp1 HG02451.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1547-210delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138924295 | |||||
| chr5:138924296
|
A | T | 57 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(54): Show | 57 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.1547-214A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138924296 | ||||||
| chr5:138924301
|
C | A | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1547-209C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138924301 | ||||||
| chr5:138924907
|
G | A | 2 | a0001c0001t0007g0111a0001c0001t0007g0112 | 2 | HG01099.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.1747+197G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 12/17 | chr5 | 138924907 | ||||||
| chr5:138924916
|
C | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | NA18946.hp2 NA19003.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1747+206C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 12/17 | chr5 | 138924916 | ||||||
| chr5:138925114
|
A | G | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1748-142A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 12/17 | chr5 | 138925114 | ||||||
| chr5:138925425
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1899+18A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138925425 | ||||||
| chr5:138925765
|
T | C | 1 | a0001c0002t0008g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1899+358T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138925765 | ||||||
| chr5:138925859
|
T | G | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1899+452T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138925859 | ||||||
| chr5:138925982
|
C | T | 49 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(46): Show | 49 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.1899+575C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138925982 | ||||||
| chr5:138926060
|
T | C | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1899+653T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138926060 | ||||||
| chr5:138926172
|
C | T | 2 | a0001c0001t0006g0174a0001c0001t0006g0175 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1899+765C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138926172 | ||||||
| chr5:138926187
|
C | A | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1899+780C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138926187 | ||||||
| chr5:138926301
|
A | G | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1899+894A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138926301 | ||||||
| chr5:138926526
|
G | A | 1 | a0001c0002t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1899+1119G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138926526 | ||||||
| chr5:138926546
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0097 | 2 | HG01243.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1899+1139G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138926546 | ||||||
| chr5:138926601
|
G | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(12): Show | 15 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1899+1194G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138926601 | ||||||
| chr5:138926728
|
GA | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(11): Show | 14 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1899+1330delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 138926728 | |||||
| chr5:138926910
|
A | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1899+1503A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138926910 | ||||||
| chr5:138926967
|
G | A | 2 | a0001c0002t0002g0002a0001c0002t0002g0003 | 2 | HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1899+1560G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138926967 | ||||||
| chr5:138926981
|
A | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(54): Show | 57 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.1899+1574A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138926981 | ||||||
| chr5:138927102
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1899+1695C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927102 | ||||||
| chr5:138927126
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1899+1719A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927126 | ||||||
| chr5:138927211
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1899+1804C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927211 | ||||||
| chr5:138927439
|
T | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.1900-1807T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927439 | ||||||
| chr5:138927442
|
C | T | 1 | a0001c0002t0003g0029 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1900-1804C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927442 | ||||||
| chr5:138927478
|
C | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1900-1768C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927478 | ||||||
| chr5:138927560
|
G | A | 36 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(33): Show | 36 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1900-1686G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927560 | ||||||
| chr5:138927710
|
T | TAATG | 29 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0045others(26): Show | 29 | HG00099.hp2 HG00741.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1900-1502_1900-149 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 138927710 | |||||
| chr5:138927710
|
T | TAATGAAT others(1): Show |
7 | a0001c0001t0001g0088a0001c0001t0001g0149a0001c0002t0003g0004others(4): Show | 7 | HG01167.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1900-1506_1900-149 others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 138927710 | |||||
| chr5:138927710
|
TAATG | T | 8 | a0001c0001t0001g0171a0001c0002t0003g0021a0001c0002t0003g0022others(5): Show | 8 | HG01109.hp2 HG01361.hp1 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.1900-1502_1900-149 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 138927710 | |||||
| chr5:138927710
|
TAATGAAT others(1): Show |
T | 4 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0006g0174others(1): Show | 4 | HG01243.hp2 HG03486.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1900-1506_1900-149 others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 138927710 | |||||
| chr5:138927710
|
TAATGAAT others(7): Show |
T | 36 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(33): Show | 36 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1900-1535_1900-152 others(18): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927710 | ||||||
| chr5:138927871
|
C | T | 10 | a0001c0002t0003g0004a0001c0002t0003g0027a0001c0002t0003g0032others(7): Show | 10 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1900-1375C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927871 | ||||||
| chr5:138927916
|
T | G | 2 | a0001c0002t0002g0056a0001c0002t0002g0060 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1900-1330T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927916 | ||||||
| chr5:138927934
|
G | A | 20 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0001g0159others(17): Show | 20 | HG01070.hp1 HG01109.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1900-1312G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927934 | ||||||
| chr5:138927938
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1900-1308A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927938 | ||||||
| chr5:138928369
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 76 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.1900-877C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138928369 | ||||||
| chr5:138928387
|
CTCTTT | C | 3 | a0001c0002t0005g0026a0001c0002t0005g0050a0001c0002t0005g0068 | 3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1900-852_1900-848d others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 138928387 | |||||
| chr5:138928724
|
A | G | 1 | a0001c0002t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1900-522A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138928724 | ||||||
| chr5:138928735
|
A | G | 36 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(33): Show | 36 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1900-511A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138928735 | ||||||
| chr5:138928762
|
C | T | 15 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(12): Show | 15 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1900-484C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138928762 | ||||||
| chr5:138928790
|
C | T | 2 | a0001c0001t0006g0174a0001c0001t0006g0175 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1900-456C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138928790 | ||||||
| chr5:138928859
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1900-387C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138928859 | ||||||
| chr5:138928876
|
A | G | 2 | a0001c0001t0006g0174a0001c0001t0006g0175 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1900-370A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138928876 | ||||||
| chr5:138928931
|
G | A | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1900-315G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138928931 | ||||||
| chr5:138928940
|
G | GA | 66 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(63): Show | 66 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1900-295dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 138928940 | |||||
| chr5:138928973
|
T | C | 10 | a0001c0002t0003g0004a0001c0002t0003g0027a0001c0002t0003g0032others(7): Show | 10 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1900-273T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138928973 | ||||||
| chr5:138929030
|
C | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0138 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1900-216C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138929030 | ||||||
| chr5:138929105
|
T | C | 2 | a0001c0004t0004g0005a0001c0009t0004g0006 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1900-141T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138929105 | ||||||
| chr5:138929222
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1900-24C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138929222 | ||||||
| chr5:138929476
|
G | A | 11 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(8): Show | 11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2010+120G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 14/17 | chr5 | 138929476 | ||||||
| chr5:138929867
|
T | C | 3 | a0001c0002t0003g0029a0001c0002t0008g0028a0001c0013t0003g0031 | 3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2010+511T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 14/17 | chr5 | 138929867 | ||||||
| chr5:138930208
|
G | A | 3 | a0001c0002t0002g0066a0001c0002t0002g0067a0001c0002t0002g0083 | 3 | HG00323.hp1 HG00639.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.2011-265G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 14/17 | chr5 | 138930208 | ||||||
| chr5:138930377
|
A | G | 10 | a0001c0002t0003g0004a0001c0002t0003g0027a0001c0002t0003g0032others(7): Show | 10 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.2011-96A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 14/17 | chr5 | 138930377 | ||||||
| chr5:138930399
|
A | C | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2011-74A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 14/17 | chr5 | 138930399 | ||||||
| chr5:138930696
|
T | A | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2192+42T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 15/17 | chr5 | 138930696 | ||||||
| chr5:138931188
|
C | T | 1 | a0001c0002t0003g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2298+253C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138931188 | ||||||
| chr5:138931252
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2298+317C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138931252 | ||||||
| chr5:138931358
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2298+423G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138931358 | ||||||
| chr5:138931374
|
A | G | 1 | a0001c0009t0004g0006 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2298+439A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138931374 | ||||||
| chr5:138931394
|
T | C | 73 | a0001c0001t0001g0039a0001c0001t0001g0086a0001c0001t0001g0087others(70): Show | 73 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.2298+459T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138931394 | ||||||
| chr5:138931525
|
T | G | 23 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(20): Show | 23 | HG00423.hp1 HG01109.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.2298+590T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138931525 | ||||||
| chr5:138931688
|
G | A | 60 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(57): Show | 60 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.2298+753G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138931688 | ||||||
| chr5:138932053
|
TTACTC | T | 3 | a0001c0002t0003g0032a0001c0002t0003g0033a0001c0002t0003g0034 | 3 | HG00741.hp1 HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2299-524_2299-520d others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138932053 | ||||||
| chr5:138932127
|
A | G | 76 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(73): Show | 76 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.2299-451A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138932127 | ||||||
| chr5:138932289
|
G | A | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2299-289G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138932289 | ||||||
| chr5:138932376
|
G | A | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2299-202G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138932376 | ||||||
| chr5:138932503
|
T | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.2299-75T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138932503 | ||||||
| chr5:138933111
|
G | C | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2433+399G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 17/17 | chr5 | 138933111 | ||||||
| chr5:138933130
|
TCAAAA | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0017 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2433+425_2433+429d others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr5 | 138933130 | |||||
| chr5:138933141
|
C | T | 4 | a0001c0001t0001g0088a0001c0001t0001g0149a0003c0007t0001g0099others(1): Show | 4 | HG02723.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2433+429C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 17/17 | chr5 | 138933141 | ||||||
| chr5:138933293
|
T | C | 4 | a0001c0004t0004g0005a0001c0004t0004g0007a0001c0004t0004g0180others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2434-509T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 17/17 | chr5 | 138933293 | ||||||
| chr5:138933316
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2434-486A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 17/17 | chr5 | 138933316 | ||||||
| chr5:138933459
|
G | A | 37 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0035others(34): Show | 37 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.2434-343G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 17/17 | chr5 | 138933459 | ||||||
| chr5:138933609
|
G | A | 1 | a0001c0001t0006g0174 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2434-193G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 17/17 | chr5 | 138933609 | ||||||
| chr5:138933653
|
C | G | 1 | a0001c0009t0004g0006 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2434-149C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 17/17 | chr5 | 138933653 | ||||||
| chr5:138933774
|
C | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.2434-28C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 17/17 | chr5 | 138933774 |