Search by Gene
| geneid | 306 |
|---|---|
| ensemblid | ENSG00000138772.13 |
| hgncid | 541 |
| symbol | ANXA3 |
| name | annexin A3 |
| refseq_nuc | NM_005139.3 |
| refseq_prot | NP_005130.1 |
| ensembl_nuc | ENST00000264908.11 |
| ensembl_prot | ENSP00000264908.6 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 78551770 |
| end | 78610447 |
| strand | + |
| ver | v1.2 |
| region | chr4:78551770-78610447 |
| region5000 | chr4:78546770-78615447 |
| regionname0 | ANXA3_chr4_78551770_78610447 |
| regionname5000 | ANXA3_chr4_78546770_78615447 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| 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 | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 323 | 313 | 83 | 48 | 144 | 6 | 30 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0002 | 0/0 | 323 | 6 | 6 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0003 | 0/0 | 323 | 4 | 4 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0004 | 0/0 | 323 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0005 | 0/0 | 323 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0006 | 0/0 | 323 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0007 | 0/0 | 323 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0008 | 0/0 | 323 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0009 | 0/0 | 323 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 972 | 287 | 58 | 48 | 143 | 6 | 30 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| c0002 | 0/0 | 972 | 23 | 23 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| c0003 | 0/0 | 972 | 6 | 6 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| c0004 | 0/0 | 972 | 4 | 4 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| c0005 | 0/0 | 972 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| c0006 | 0/0 | 972 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| c0007 | 0/0 | 972 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| c0008 | 0/0 | 972 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| c0009 | 0/0 | 972 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| c0010 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| c0011 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| c0012 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| c0013 | 0/0 | 972 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| thapid | 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
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 461 | 144 | 30 | 16 | 81 | 3 | 13 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| t0002 | 1/0 | 461 | 78 | 23 | 26 | 15 | 2 | 11 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| t0003 | 0/0 | 461 | 71 | 6 | 6 | 50 | 1 | 8 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| t0004 | 0/0 | 461 | 18 | 18 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| t0005 | 0/0 | 461 | 9 | 9 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| t0006 | 0/0 | 458 | 8 | 8 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| t0007 | 0/0 | 461 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| t0008 | 0/0 | 461 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| achapid | ahapid | 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 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 287 | 58 | 48 | 143 | 6 | 30 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/0 | 23 | 23 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0001c0006 | a0001 | c0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0001c0011 | a0001 | c0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0001c0012 | a0001 | c0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0002c0003 | a0002 | c0003 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0003c0004 | a0003 | c0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0004c0005 | a0004 | c0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0005c0009 | a0005 | c0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0006c0008 | a0006 | c0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0007c0007 | a0007 | c0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0008c0010 | a0008 | c0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0009c0013 | a0009 | c0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| acthapid | ahapid | chapid | thapid | 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 | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/1 | 124 | 13 | 16 | 78 | 3 | 13 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 1/0 | 76 | 22 | 26 | 15 | 2 | 10 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 66 | 2 | 6 | 50 | 1 | 7 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0001c0002t0001 | a0001 | c0002 | t0001 | 0/0 | 16 | 16 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0001c0002t0003 | a0001 | c0002 | t0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0001c0002t0004 | a0001 | c0002 | t0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0001c0002t0006 | a0001 | c0002 | t0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0001c0006t0001 | a0001 | c0006 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0001c0011t0008 | a0001 | c0011 | t0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0001c0012t0001 | a0001 | c0012 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0002c0003t0004 | a0002 | c0003 | t0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0002c0003t0006 | a0002 | c0003 | t0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0003c0004t0002 | a0003 | c0004 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0003c0004t0004 | a0003 | c0004 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0003c0004t0006 | a0003 | c0004 | t0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0004c0005t0003 | a0004 | c0005 | t0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0005c0009t0001 | a0005 | c0009 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0006c0008t0002 | a0006 | c0008 | t0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0007c0007t0001 | a0007 | c0007 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0008c0010t0004 | a0008 | c0010 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| a0009c0013t0003 | a0009 | c0013 | t0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | copy fasta |
| actghapid | ahapid | chapid | thapid | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0006 | a0001 | c0001 | t0001 | g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0115 | a0001 | c0001 | t0001 | g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0174 | a0001 | c0001 | t0001 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0175 | a0001 | c0001 | t0001 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0184 | a0001 | c0001 | t0001 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0194 | a0001 | c0001 | t0001 | g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0196 | a0001 | c0001 | t0001 | g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0200 | a0001 | c0001 | t0001 | g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0201 | a0001 | c0001 | t0001 | g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0202 | a0001 | c0001 | t0001 | g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0211 | a0001 | c0001 | t0001 | g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0213 | a0001 | c0001 | t0001 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0215 | a0001 | c0001 | t0001 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0216 | a0001 | c0001 | t0001 | g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0217 | a0001 | c0001 | t0001 | g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0219 | a0001 | c0001 | t0001 | g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0220 | a0001 | c0001 | t0001 | g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0223 | a0001 | c0001 | t0001 | g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0224 | a0001 | c0001 | t0001 | g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0226 | a0001 | c0001 | t0001 | g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0229 | a0001 | c0001 | t0001 | g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0231 | a0001 | c0001 | t0001 | g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0232 | a0001 | c0001 | t0001 | g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0233 | a0001 | c0001 | t0001 | g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0234 | a0001 | c0001 | t0001 | g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0235 | a0001 | c0001 | t0001 | g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0236 | a0001 | c0001 | t0001 | g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0237 | a0001 | c0001 | t0001 | g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0238 | a0001 | c0001 | t0001 | g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0240 | a0001 | c0001 | t0001 | g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0241 | a0001 | c0001 | t0001 | g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0242 | a0001 | c0001 | t0001 | g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0243 | a0001 | c0001 | t0001 | g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0244 | a0001 | c0001 | t0001 | g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0245 | a0001 | c0001 | t0001 | g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0246 | a0001 | c0001 | t0001 | g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0247 | a0001 | c0001 | t0001 | g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0249 | a0001 | c0001 | t0001 | g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0250 | a0001 | c0001 | t0001 | g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0251 | a0001 | c0001 | t0001 | g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0253 | a0001 | c0001 | t0001 | g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0254 | a0001 | c0001 | t0001 | g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0255 | a0001 | c0001 | t0001 | g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0256 | a0001 | c0001 | t0001 | g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0258 | a0001 | c0001 | t0001 | g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0268 | a0001 | c0001 | t0001 | g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0269 | a0001 | c0001 | t0001 | g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0270 | a0001 | c0001 | t0001 | g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0272 | a0001 | c0001 | t0001 | g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0277 | a0001 | c0001 | t0001 | g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0278 | a0001 | c0001 | t0001 | g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0279 | a0001 | c0001 | t0001 | g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0280 | a0001 | c0001 | t0001 | g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0282 | a0001 | c0001 | t0001 | g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0283 | a0001 | c0001 | t0001 | g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0289 | a0001 | c0001 | t0001 | g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0290 | a0001 | c0001 | t0001 | g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0291 | a0001 | c0001 | t0001 | g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0293 | a0001 | c0001 | t0001 | g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0295 | a0001 | c0001 | t0001 | g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0297 | a0001 | c0001 | t0001 | g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0298 | a0001 | c0001 | t0001 | g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0299 | a0001 | c0001 | t0001 | g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0303 | a0001 | c0001 | t0001 | g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0307 | a0001 | c0001 | t0001 | g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0001g0308 | a0001 | c0001 | t0001 | g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0001 | a0001 | c0001 | t0002 | g0001 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0007 | a0001 | c0001 | t0002 | g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0011 | a0001 | c0001 | t0002 | g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0015 | a0001 | c0001 | t0002 | g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0017 | a0001 | c0001 | t0002 | g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0020 | a0001 | c0001 | t0002 | g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0026 | a0001 | c0001 | t0002 | g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0027 | a0001 | c0001 | t0002 | g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0028 | a0001 | c0001 | t0002 | g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0029 | a0001 | c0001 | t0002 | g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0030 | a0001 | c0001 | t0002 | g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0031 | a0001 | c0001 | t0002 | g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0033 | a0001 | c0001 | t0002 | g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0035 | a0001 | c0001 | t0002 | g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0053 | a0001 | c0001 | t0002 | g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0054 | a0001 | c0001 | t0002 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0055 | a0001 | c0001 | t0002 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0056 | a0001 | c0001 | t0002 | g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0058 | a0001 | c0001 | t0002 | g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0059 | a0001 | c0001 | t0002 | g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0062 | a0001 | c0001 | t0002 | g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0085 | a0001 | c0001 | t0002 | g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0086 | a0001 | c0001 | t0002 | g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0087 | a0001 | c0001 | t0002 | g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0088 | a0001 | c0001 | t0002 | g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0089 | a0001 | c0001 | t0002 | g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0092 | a0001 | c0001 | t0002 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0099 | a0001 | c0001 | t0002 | g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0100 | a0001 | c0001 | t0002 | g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0101 | a0001 | c0001 | t0002 | g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0106 | a0001 | c0001 | t0002 | g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0107 | a0001 | c0001 | t0002 | g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0108 | a0001 | c0001 | t0002 | g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0110 | a0001 | c0001 | t0002 | g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0117 | a0001 | c0001 | t0002 | g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0118 | a0001 | c0001 | t0002 | g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0119 | a0001 | c0001 | t0002 | g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0143 | a0001 | c0001 | t0002 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0144 | a0001 | c0001 | t0002 | g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0156 | a0001 | c0001 | t0002 | g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0158 | a0001 | c0001 | t0002 | g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0159 | a0001 | c0001 | t0002 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0161 | a0001 | c0001 | t0002 | g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0162 | a0001 | c0001 | t0002 | g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0163 | a0001 | c0001 | t0002 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0164 | a0001 | c0001 | t0002 | g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0167 | a0001 | c0001 | t0002 | g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0183 | a0001 | c0001 | t0002 | g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0185 | a0001 | c0001 | t0002 | g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0197 | a0001 | c0001 | t0002 | g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0198 | a0001 | c0001 | t0002 | g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0205 | a0001 | c0001 | t0002 | g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0206 | a0001 | c0001 | t0002 | g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0207 | a0001 | c0001 | t0002 | g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0208 | a0001 | c0001 | t0002 | g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0209 | a0001 | c0001 | t0002 | g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0210 | a0001 | c0001 | t0002 | g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0212 | a0001 | c0001 | t0002 | g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0221 | a0001 | c0001 | t0002 | g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0225 | a0001 | c0001 | t0002 | g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0264 | a0001 | c0001 | t0002 | g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0266 | a0001 | c0001 | t0002 | g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0267 | a0001 | c0001 | t0002 | g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0281 | a0001 | c0001 | t0002 | g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0284 | a0001 | c0001 | t0002 | g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0285 | a0001 | c0001 | t0002 | g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0286 | a0001 | c0001 | t0002 | g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0287 | a0001 | c0001 | t0002 | g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0301 | a0001 | c0001 | t0002 | g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0002g0310 | a0001 | c0001 | t0002 | g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0002 | a0001 | c0001 | t0003 | g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0009 | a0001 | c0001 | t0003 | g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0010 | a0001 | c0001 | t0003 | g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0016 | a0001 | c0001 | t0003 | g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0018 | a0001 | c0001 | t0003 | g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0036 | a0001 | c0001 | t0003 | g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0078 | a0001 | c0001 | t0003 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0079 | a0001 | c0001 | t0003 | g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0080 | a0001 | c0001 | t0003 | g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0083 | a0001 | c0001 | t0003 | g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0094 | a0001 | c0001 | t0003 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0098 | a0001 | c0001 | t0003 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0104 | a0001 | c0001 | t0003 | g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0112 | a0001 | c0001 | t0003 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0113 | a0001 | c0001 | t0003 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0120 | a0001 | c0001 | t0003 | g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0123 | a0001 | c0001 | t0003 | g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0135 | a0001 | c0001 | t0003 | g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0136 | a0001 | c0001 | t0003 | g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0138 | a0001 | c0001 | t0003 | g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0139 | a0001 | c0001 | t0003 | g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0140 | a0001 | c0001 | t0003 | g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0145 | a0001 | c0001 | t0003 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0168 | a0001 | c0001 | t0003 | g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0170 | a0001 | c0001 | t0003 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0171 | a0001 | c0001 | t0003 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0172 | a0001 | c0001 | t0003 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0176 | a0001 | c0001 | t0003 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0178 | a0001 | c0001 | t0003 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0179 | a0001 | c0001 | t0003 | g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0180 | a0001 | c0001 | t0003 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0181 | a0001 | c0001 | t0003 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0182 | a0001 | c0001 | t0003 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0186 | a0001 | c0001 | t0003 | g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0187 | a0001 | c0001 | t0003 | g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0188 | a0001 | c0001 | t0003 | g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0190 | a0001 | c0001 | t0003 | g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0191 | a0001 | c0001 | t0003 | g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0192 | a0001 | c0001 | t0003 | g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0193 | a0001 | c0001 | t0003 | g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0195 | a0001 | c0001 | t0003 | g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0199 | a0001 | c0001 | t0003 | g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0203 | a0001 | c0001 | t0003 | g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0204 | a0001 | c0001 | t0003 | g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0214 | a0001 | c0001 | t0003 | g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0218 | a0001 | c0001 | t0003 | g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0222 | a0001 | c0001 | t0003 | g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0227 | a0001 | c0001 | t0003 | g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0230 | a0001 | c0001 | t0003 | g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0239 | a0001 | c0001 | t0003 | g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0248 | a0001 | c0001 | t0003 | g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0257 | a0001 | c0001 | t0003 | g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0265 | a0001 | c0001 | t0003 | g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0271 | a0001 | c0001 | t0003 | g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0273 | a0001 | c0001 | t0003 | g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0274 | a0001 | c0001 | t0003 | g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0275 | a0001 | c0001 | t0003 | g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0276 | a0001 | c0001 | t0003 | g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0292 | a0001 | c0001 | t0003 | g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0294 | a0001 | c0001 | t0003 | g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0003g0311 | a0001 | c0001 | t0003 | g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0004g0022 | a0001 | c0001 | t0004 | g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0004g0043 | a0001 | c0001 | t0004 | g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0004g0060 | a0001 | c0001 | t0004 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0004g0061 | a0001 | c0001 | t0004 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0004g0068 | a0001 | c0001 | t0004 | g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0004g0076 | a0001 | c0001 | t0004 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0004g0147 | a0001 | c0001 | t0004 | g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0004g0148 | a0001 | c0001 | t0004 | g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0004g0153 | a0001 | c0001 | t0004 | g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0004g0288 | a0001 | c0001 | t0004 | g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0005g0023 | a0001 | c0001 | t0005 | g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0005g0046 | a0001 | c0001 | t0005 | g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0005g0047 | a0001 | c0001 | t0005 | g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0005g0141 | a0001 | c0001 | t0005 | g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0005g0259 | a0001 | c0001 | t0005 | g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0005g0260 | a0001 | c0001 | t0005 | g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0005g0261 | a0001 | c0001 | t0005 | g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0005g0262 | a0001 | c0001 | t0005 | g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0005g0263 | a0001 | c0001 | t0005 | g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0006g0057 | a0001 | c0001 | t0006 | g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0001t0007g0154 | a0001 | c0001 | t0007 | g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0001g0019 | a0001 | c0002 | t0001 | g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0001g0037 | a0001 | c0002 | t0001 | g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0001g0039 | a0001 | c0002 | t0001 | g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0001g0041 | a0001 | c0002 | t0001 | g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0001g0052 | a0001 | c0002 | t0001 | g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0001g0063 | a0001 | c0002 | t0001 | g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0001g0064 | a0001 | c0002 | t0001 | g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0001g0065 | a0001 | c0002 | t0001 | g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0001g0066 | a0001 | c0002 | t0001 | g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0001g0067 | a0001 | c0002 | t0001 | g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0001g0069 | a0001 | c0002 | t0001 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0001g0077 | a0001 | c0002 | t0001 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0001g0152 | a0001 | c0002 | t0001 | g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0001g0304 | a0001 | c0002 | t0001 | g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0001g0305 | a0001 | c0002 | t0001 | g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0001g0306 | a0001 | c0002 | t0001 | g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0003g0038 | a0001 | c0002 | t0003 | g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0003g0050 | a0001 | c0002 | t0003 | g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0004g0040 | a0001 | c0002 | t0004 | g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0004g0042 | a0001 | c0002 | t0004 | g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0004g0151 | a0001 | c0002 | t0004 | g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0006g0149 | a0001 | c0002 | t0006 | g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0002t0006g0300 | a0001 | c0002 | t0006 | g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0006t0001g0252 | a0001 | c0006 | t0001 | g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0011t0008g0074 | a0001 | c0011 | t0008 | g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0001c0012t0001g0302 | a0001 | c0012 | t0001 | g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0002c0003t0004g0048 | a0002 | c0003 | t0004 | g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0002c0003t0004g0049 | a0002 | c0003 | t0004 | g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0002c0003t0004g0150 | a0002 | c0003 | t0004 | g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0002c0003t0006g0005 | a0002 | c0003 | t0006 | g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0002c0003t0006g0137 | a0002 | c0003 | t0006 | g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0003c0004t0002g0072 | a0003 | c0004 | t0002 | g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0003c0004t0004g0309 | a0003 | c0004 | t0004 | g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0003c0004t0006g0071 | a0003 | c0004 | t0006 | g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0003c0004t0006g0073 | a0003 | c0004 | t0006 | g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0004c0005t0003g0051 | a0004 | c0005 | t0003 | g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0004c0005t0003g0070 | a0004 | c0005 | t0003 | g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0005c0009t0001g0189 | a0005 | c0009 | t0001 | g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0006c0008t0002g0134 | a0006 | c0008 | t0002 | g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0007c0007t0001g0296 | a0007 | c0007 | t0001 | g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0008c0010t0004g0157 | a0008 | c0010 | t0004 | g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| a0009c0013t0003g0228 | a0009 | c0013 | t0003 | g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0100 | EUR | GBR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | GBR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0198 | EUR | FIN | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0278 | EUR | FIN | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0139 | EUR | FIN | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | FIN | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00423 | hp1 | a0001 | c0006 | t0001 | g0252 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0140 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0120 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | CLM | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01884 | hp1 | a0003 | c0004 | t0004 | g0309 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0261 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01891 | hp1 | a0001 | c0002 | t0006 | g0149 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01891 | hp2 | a0008 | c0010 | t0004 | g0157 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0239 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0230 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02145 | hp2 | a0002 | c0003 | t0004 | g0048 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CDX | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02155 | hp2 | a0007 | c0007 | t0001 | g0296 | EAS | CDX | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02258 | hp1 | a0002 | c0003 | t0006 | g0137 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0047 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0123 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0064 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02280 | hp2 | a0003 | c0004 | t0006 | g0071 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0294 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0148 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02572 | hp2 | a0002 | c0003 | t0004 | g0049 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0285 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0060 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0262 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0259 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02717 | hp2 | a0001 | c0002 | t0004 | g0151 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02809 | hp1 | a0002 | c0003 | t0004 | g0150 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02818 | hp1 | a0003 | c0004 | t0002 | g0072 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0305 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0069 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0306 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0286 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0141 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02976 | hp1 | a0001 | c0002 | t0006 | g0300 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0057 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0288 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03195 | hp2 | a0001 | c0002 | t0003 | g0038 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0263 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0065 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0304 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03486 | hp1 | a0001 | c0002 | t0004 | g0040 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03486 | hp2 | a0004 | c0005 | t0003 | g0070 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03516 | hp1 | a0001 | c0011 | t0008 | g0074 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03516 | hp2 | a0001 | c0002 | t0004 | g0042 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0154 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0061 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0077 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | STU | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0104 | SAS | STU | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0080 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | BEB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03831 | hp2 | a0009 | c0013 | t0003 | g0228 | SAS | BEB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0079 | SAS | BEB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | BEB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0311 | SAS | STU | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | STU | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0083 | SAS | STU | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | STU | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0265 | SAS | STU | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG04204 | hp2 | a0006 | c0008 | t0002 | g0134 | SAS | STU | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0138 | SAS | STU | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | STU | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18522 | hp1 | a0003 | c0004 | t0006 | g0073 | AFR | YRI | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | YRI | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18612 | hp1 | a0005 | c0009 | t0001 | g0189 | EAS | CHB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | CHB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | YRI | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18906 | hp2 | a0002 | c0003 | t0006 | g0005 | AFR | YRI | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19030 | hp1 | a0001 | c0012 | t0001 | g0302 | AFR | LWK | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | LWK | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | LWK | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19043 | hp2 | a0004 | c0005 | t0003 | g0051 | AFR | LWK | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0043 | AFR | YRI | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | YRI | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA20129 | hp1 | a0002 | c0003 | t0006 | g0005 | AFR | ASW | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0260 | AFR | ASW | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0310 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG02559 | hp2 | a0001 | c0002 | t0003 | g0050 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0152 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0063 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | USA | ANXA3_chr4_78546770_78615447 | ANXA3 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | USA | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | USA | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0068 | AFR | USA | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | LWK | ANXA3_chr4_78546770_78615447 | ANXA3 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0076 | AFR | LWK | ANXA3_chr4_78546770_78615447 | ANXA3 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0194 | REF | REF | ANXA3_chr4_78546770_78615447 | ANXA3 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0001 | REF | REF | ANXA3_chr4_78546770_78615447 | ANXA3 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:78573220
|
G | A | 1 | a0003 | 4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
missense_variant | MODERATE | c.56G>A | p.Ser19Asn | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/13 | 184/1432 | 56/972 | 19/323 | chr4 | 78573220 | ||
| chr4:78579027
|
G | T | 1 | a0009 | 1 | HG03831.hp2 | missense_variant&splice_region_variant | MODERATE | c.104G>T | p.Gly35Val | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/13 | 232/1432 | 104/972 | 35/323 | chr4 | 78579027 | ||
| chr4:78586263
|
G | A | 1 | a0007 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.316G>A | p.Ala106Thr | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/13 | 444/1432 | 316/972 | 106/323 | chr4 | 78586263 | ||
| chr4:78586264
|
C | T | 1 | a0008 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.317C>T | p.Ala106Val | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/13 | 445/1432 | 317/972 | 106/323 | chr4 | 78586264 | ||
| chr4:78586326
|
G | A | 1 | a0006 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.379G>A | p.Asp127Asn | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/13 | 507/1432 | 379/972 | 127/323 | chr4 | 78586326 | ||
| chr4:78597340
|
T | A | 1 | a0002 | 6 | HG02145.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
missense_variant | MODERATE | c.656T>A | p.Ile219Asn | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/13 | 784/1432 | 656/972 | 219/323 | chr4 | 78597340 | ||
| chr4:78601528
|
C | T | 1 | a0005 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.749C>T | p.Thr250Met | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/13 | 877/1432 | 749/972 | 250/323 | chr4 | 78601528 | ||
| chr4:78610081
|
T | C | 1 | a0004 | 2 | HG03486.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.938T>C | p.Ile313Thr | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 13/13 | 1066/1432 | 938/972 | 313/323 | chr4 | 78610081 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:78579031
|
T | A | 1 | a0009c0013 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.108T>A | p.Thr36Thr | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/13 | 236/1432 | 108/972 | 36/323 | chr4 | 78579031 | ||
| chr4:78579073
|
T | C | 1 | a0001c0006 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.150T>C | p.Asn50Asn | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/13 | 278/1432 | 150/972 | 50/323 | chr4 | 78579073 | ||
| chr4:78582248
|
A | G | 3 | a0001c0002a0001c0011a0001c0012 | 25 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(22): Show |
synonymous_variant | LOW | c.270A>G | p.Pro90Pro | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/13 | 398/1432 | 270/972 | 90/323 | chr4 | 78582248 | ||
| chr4:78586265
|
G | T | 3 | a0001c0002a0001c0011a0001c0012 | 25 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(22): Show |
synonymous_variant | LOW | c.318G>T | p.Ala106Ala | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/13 | 446/1432 | 318/972 | 106/323 | chr4 | 78586265 | ||
| chr4:78591578
|
C | T | 1 | a0001c0012 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.438C>T | p.Ser146Ser | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/13 | 566/1432 | 438/972 | 146/323 | chr4 | 78591578 | ||
| chr4:78597320
|
A | G | 1 | a0001c0011 | 1 | HG03516.hp1 | splice_region_variant&synonymous_variant | LOW | c.636A>G | p.Thr212Thr | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/13 | 764/1432 | 636/972 | 212/323 | chr4 | 78597320 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:78551791
|
C | G | 1 | a0001c0011t0008 | 1 | HG03516.hp1 | 5_prime_UTR_variant | MODIFIER | c.-107C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/13 | 2683 | chr4 | 78551791 | |||||
| chr4:78610154
|
C | T | 7 | a0001c0001t0001a0001c0002t0001a0001c0006t0001others(4): Show | 145 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*39C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 13/13 | 39 | chr4 | 78610154 | |||||
| chr4:78610227
|
T | G | 6 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(3): Show | 81 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*112T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 13/13 | 112 | chr4 | 78610227 | |||||
| chr4:78610250
|
TAAC | T | 4 | a0001c0001t0006a0001c0002t0006a0002c0003t0006others(1): Show | 8 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*147_*149delCAA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 13/13 | 147 | INFO_REALIGN_3_PRIME | chr4 | 78610250 | ||||
| chr4:78610367
|
T | A | 1 | a0001c0001t0005 | 9 | HG01884.hp2 HG02258.hp2 HG02630.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*252T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 13/13 | 252 | chr4 | 78610367 | |||||
| chr4:78610399
|
C | A | 22 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(19): Show | 252 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*284C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 13/13 | 284 | chr4 | 78610399 | |||||
| chr4:78610434
|
T | G | 1 | a0001c0001t0007 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*319T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 13/13 | 319 | chr4 | 78610434 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:78551902
|
A | C | 282 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0012others(279): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-39+43A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78551902 | ||||||
| chr4:78551949
|
G | T | 1 | a0001c0001t0003g0311 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-39+90G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78551949 | ||||||
| chr4:78551982
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-39+123G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78551982 | ||||||
| chr4:78552035
|
C | G | 251 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0012others(248): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-39+176C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552035 | ||||||
| chr4:78552121
|
G | A | 71 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0044others(68): Show | 74 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.-39+262G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552121 | ||||||
| chr4:78552130
|
G | A | 1 | a0001c0001t0005g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-39+271G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552130 | ||||||
| chr4:78552216
|
C | T | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG00323.hp1 HG01106.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-39+357C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552216 | ||||||
| chr4:78552240
|
A | G | 71 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0044others(68): Show | 74 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.-39+381A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552240 | ||||||
| chr4:78552314
|
C | T | 1 | a0001c0001t0002g0310 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-39+455C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552314 | ||||||
| chr4:78552369
|
T | C | 75 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0044others(72): Show | 78 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.-39+510T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552369 | ||||||
| chr4:78552417
|
G | A | 10 | a0001c0001t0001g0045a0001c0001t0002g0053a0001c0001t0002g0054others(7): Show | 10 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-39+558G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552417 | ||||||
| chr4:78552458
|
T | C | 10 | a0001c0001t0001g0045a0001c0001t0002g0053a0001c0001t0002g0054others(7): Show | 10 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-39+599T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552458 | ||||||
| chr4:78552529
|
T | C | 1 | a0001c0001t0003g0018 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-39+670T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552529 | ||||||
| chr4:78552548
|
A | G | 76 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0044others(73): Show | 79 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-39+689A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552548 | ||||||
| chr4:78552580
|
TA | T | 75 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0044others(72): Show | 78 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.-39+722delA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552580 | ||||||
| chr4:78552643
|
C | A | 72 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0044others(69): Show | 75 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.-39+784C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552643 | ||||||
| chr4:78552886
|
C | A | 199 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(196): Show | 211 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-39+1027C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552886 | ||||||
| chr4:78553075
|
T | A | 1 | a0001c0001t0001g0044 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-39+1216T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553075 | ||||||
| chr4:78553161
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-38-1275C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553161 | ||||||
| chr4:78553237
|
C | A | 1 | a0001c0001t0001g0146 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-38-1199C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553237 | ||||||
| chr4:78553306
|
G | A | 2 | a0001c0001t0004g0147a0001c0001t0004g0148 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-38-1130G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553306 | ||||||
| chr4:78553349
|
A | T | 151 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0012others(148): Show | 161 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.-38-1087A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553349 | ||||||
| chr4:78553428
|
C | T | 4 | a0001c0001t0001g0295a0001c0001t0001g0297a0001c0001t0001g0298others(1): Show | 4 | HG02129.hp2 HG02155.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38-1008C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553428 | ||||||
| chr4:78553471
|
A | G | 8 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0007others(5): Show | 9 | HG00733.hp1 HG01070.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.-38-965A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553471 | ||||||
| chr4:78553552
|
T | C | 6 | a0001c0001t0004g0153a0001c0001t0007g0154a0001c0002t0001g0152others(3): Show | 6 | HG01891.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38-884T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553552 | ||||||
| chr4:78553613
|
T | C | 10 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0039others(7): Show | 10 | HG02145.hp1 HG02723.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38-823T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553613 | ||||||
| chr4:78553658
|
A | T | 6 | a0001c0001t0004g0153a0001c0001t0007g0154a0001c0002t0001g0152others(3): Show | 6 | HG01891.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38-778A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553658 | ||||||
| chr4:78553665
|
A | G | 75 | a0001c0001t0001g0045a0001c0001t0001g0075a0001c0001t0001g0114others(72): Show | 79 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.-38-771A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553665 | ||||||
| chr4:78553681
|
C | G | 5 | a0001c0001t0001g0024a0001c0001t0004g0022a0001c0001t0004g0060others(2): Show | 5 | HG02622.hp2 HG02886.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38-755C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553681 | ||||||
| chr4:78553732
|
T | G | 221 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(218): Show | 236 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.-38-704T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553732 | ||||||
| chr4:78553808
|
C | A | 20 | a0001c0001t0001g0024a0001c0001t0002g0053a0001c0001t0002g0054others(17): Show | 21 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.-38-628C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553808 | ||||||
| chr4:78553900
|
C | A | 2 | a0001c0001t0004g0060a0001c0001t0004g0061 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-38-536C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553900 | ||||||
| chr4:78554192
|
A | AT | 14 | a0001c0001t0004g0076a0001c0002t0001g0019a0001c0002t0001g0037others(11): Show | 14 | HG02145.hp1 HG02280.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.-38-237dupT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 78554192 | |||||
| chr4:78554288
|
A | G | 4 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0002t0006g0300others(1): Show | 4 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38-148A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78554288 | ||||||
| chr4:78554403
|
T | C | 1 | a0001c0002t0001g0304 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-38-33T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78554403 | ||||||
| chr4:78554606
|
A | T | 3 | a0001c0001t0001g0211a0001c0001t0002g0212a0001c0001t0003g0123 | 3 | HG01106.hp1 HG02273.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.15+118A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78554606 | ||||||
| chr4:78554882
|
A | G | 2 | a0001c0001t0005g0046a0001c0001t0005g0047 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.15+394A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78554882 | ||||||
| chr4:78554907
|
A | G | 215 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(212): Show | 229 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.15+419A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78554907 | ||||||
| chr4:78555032
|
C | G | 1 | a0001c0001t0001g0293 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.15+544C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555032 | ||||||
| chr4:78555036
|
T | A | 9 | a0001c0001t0001g0111a0001c0001t0001g0213a0001c0001t0001g0215others(6): Show | 9 | HG00621.hp2 HG02056.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.15+548T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555036 | ||||||
| chr4:78555248
|
T | G | 19 | a0001c0001t0001g0024a0001c0001t0002g0053a0001c0001t0002g0054others(16): Show | 20 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.15+760T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555248 | ||||||
| chr4:78555250
|
T | A | 240 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(237): Show | 255 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.15+762T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555250 | ||||||
| chr4:78555267
|
A | G | 240 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(237): Show | 255 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.15+779A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555267 | ||||||
| chr4:78555350
|
C | T | 2 | a0001c0001t0001g0291a0001c0001t0003g0292 | 2 | NA18960.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.15+862C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555350 | ||||||
| chr4:78555394
|
A | G | 1 | a0001c0001t0001g0290 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.15+906A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555394 | ||||||
| chr4:78555402
|
T | A | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00735.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.15+914T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555402 | ||||||
| chr4:78555405
|
G | A | 2 | a0001c0001t0004g0060a0001c0001t0004g0061 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.15+917G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555405 | ||||||
| chr4:78555674
|
TA | T | 29 | a0001c0001t0001g0024a0001c0001t0001g0290a0001c0001t0002g0053others(26): Show | 30 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.15+1204delA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78555674 | |||||
| chr4:78555688
|
A | AC | 3 | a0001c0001t0001g0213a0001c0001t0003g0214a0001c0011t0008g0074 | 3 | HG02056.hp2 HG02523.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.15+1200_15+1201ins others(1): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555688 | ||||||
| chr4:78555688
|
A | C | 202 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(199): Show | 216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.15+1200A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555688 | ||||||
| chr4:78555714
|
T | G | 241 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(238): Show | 256 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.15+1226T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555714 | ||||||
| chr4:78555721
|
T | C | 212 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(209): Show | 226 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.15+1233T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555721 | ||||||
| chr4:78555722
|
G | A | 211 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(208): Show | 225 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.15+1234G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555722 | ||||||
| chr4:78555852
|
T | TA | 190 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(187): Show | 204 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.15+1376dupA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78555852 | |||||
| chr4:78556141
|
G | A | 4 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0207others(1): Show | 4 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+1653G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78556141 | ||||||
| chr4:78556212
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.15+1724G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78556212 | ||||||
| chr4:78556410
|
C | G | 1 | a0001c0011t0008g0074 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.15+1922C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78556410 | ||||||
| chr4:78556700
|
C | T | 3 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0002t0001g0077 | 3 | HG02572.hp1 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.15+2212C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78556700 | ||||||
| chr4:78556781
|
C | T | 2 | a0001c0001t0005g0046a0001c0001t0005g0047 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.15+2293C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78556781 | ||||||
| chr4:78556783
|
C | G | 1 | a0001c0001t0002g0054 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.15+2295C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78556783 | ||||||
| chr4:78557145
|
G | T | 1 | a0001c0001t0001g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.15+2657G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557145 | ||||||
| chr4:78557181
|
C | T | 11 | a0001c0001t0001g0283a0001c0001t0001g0289a0001c0001t0001g0299others(8): Show | 11 | HG02486.hp1 HG02615.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+2693C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557181 | ||||||
| chr4:78557251
|
A | T | 241 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(238): Show | 256 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.15+2763A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557251 | ||||||
| chr4:78557482
|
A | G | 309 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(306): Show | 326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.15+2994A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557482 | ||||||
| chr4:78557523
|
G | C | 1 | a0001c0001t0002g0011 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.15+3035G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557523 | ||||||
| chr4:78557582
|
G | A | 6 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0088others(3): Show | 6 | HG00597.hp2 HG01928.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+3094G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557582 | ||||||
| chr4:78557636
|
C | A | 2 | a0001c0001t0005g0046a0001c0001t0005g0047 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.15+3148C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557636 | ||||||
| chr4:78557689
|
CT | C | 213 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(210): Show | 227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.15+3220delT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78557689 | |||||
| chr4:78557693
|
T | C | 14 | a0001c0001t0001g0024a0001c0001t0001g0282a0001c0001t0002g0053others(11): Show | 14 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.15+3205T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557693 | ||||||
| chr4:78557694
|
T | C | 210 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(207): Show | 224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.15+3206T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557694 | ||||||
| chr4:78557695
|
T | C | 1 | a0001c0001t0003g0292 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.15+3207T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557695 | ||||||
| chr4:78557708
|
T | C | 1 | a0001c0001t0002g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.15+3220T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557708 | ||||||
| chr4:78557844
|
A | G | 6 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0005g0046others(3): Show | 6 | HG00735.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+3356A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557844 | ||||||
| chr4:78558019
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.15+3531C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558019 | ||||||
| chr4:78558219
|
G | A | 2 | a0001c0002t0001g0063a0001c0002t0001g0064 | 2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.15+3731G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558219 | ||||||
| chr4:78558396
|
C | T | 7 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0007others(4): Show | 8 | HG00733.hp1 HG01070.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+3908C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558396 | ||||||
| chr4:78558418
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.15+3930G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558418 | ||||||
| chr4:78558510
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.15+4022G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558510 | ||||||
| chr4:78558529
|
G | A | 212 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(209): Show | 226 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.15+4041G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558529 | ||||||
| chr4:78558576
|
C | T | 4 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0002t0006g0300others(1): Show | 4 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+4088C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558576 | ||||||
| chr4:78558579
|
T | C | 201 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(198): Show | 215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.15+4091T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558579 | ||||||
| chr4:78558728
|
C | T | 211 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(208): Show | 225 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.15+4240C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558728 | ||||||
| chr4:78558762
|
A | C | 1 | a0001c0001t0003g0204 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.15+4274A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558762 | ||||||
| chr4:78558918
|
G | A | 8 | a0001c0001t0002g0053a0001c0001t0002g0054a0001c0002t0001g0052others(5): Show | 8 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+4430G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558918 | ||||||
| chr4:78559117
|
T | A | 1 | a0001c0001t0003g0145 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.15+4629T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78559117 | ||||||
| chr4:78559183
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0220 | 2 | HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.15+4695G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78559183 | ||||||
| chr4:78559255
|
A | C | 24 | a0001c0001t0001g0024a0001c0001t0002g0053a0001c0001t0002g0054others(21): Show | 25 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.15+4767A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78559255 | ||||||
| chr4:78559264
|
A | G | 212 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(209): Show | 226 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.15+4776A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78559264 | ||||||
| chr4:78559524
|
G | A | 2 | a0001c0001t0001g0308a0001c0001t0004g0043 | 2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.15+5036G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78559524 | ||||||
| chr4:78559761
|
T | C | 8 | a0001c0001t0002g0053a0001c0001t0002g0054a0001c0002t0001g0052others(5): Show | 8 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+5273T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78559761 | ||||||
| chr4:78560030
|
C | G | 4 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0002t0006g0300others(1): Show | 4 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+5542C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78560030 | ||||||
| chr4:78560055
|
C | G | 5 | a0001c0001t0001g0280a0001c0001t0001g0291a0001c0001t0002g0017others(2): Show | 6 | HG01358.hp2 HG01934.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+5567C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78560055 | ||||||
| chr4:78560374
|
T | C | 214 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(211): Show | 228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.15+5886T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78560374 | ||||||
| chr4:78560424
|
T | G | 168 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(165): Show | 182 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.15+5936T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78560424 | ||||||
| chr4:78560431
|
G | A | 8 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0039others(5): Show | 8 | HG02145.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+5943G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78560431 | ||||||
| chr4:78560603
|
G | A | 1 | a0001c0001t0002g0159 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.15+6115G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78560603 | ||||||
| chr4:78560644
|
A | C | 242 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(239): Show | 257 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.15+6156A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78560644 | ||||||
| chr4:78560840
|
C | G | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | HG00280.hp2 HG01168.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.15+6352C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78560840 | ||||||
| chr4:78560923
|
T | A | 1 | a0008c0010t0004g0157 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.15+6435T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78560923 | ||||||
| chr4:78561012
|
T | G | 304 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(301): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.15+6524T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561012 | ||||||
| chr4:78561032
|
G | A | 147 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(144): Show | 156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.15+6544G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561032 | ||||||
| chr4:78561138
|
C | T | 1 | a0001c0001t0003g0271 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.15+6650C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561138 | ||||||
| chr4:78561251
|
G | A | 1 | a0001c0001t0002g0301 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.15+6763G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561251 | ||||||
| chr4:78561255
|
A | C | 143 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(140): Show | 152 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.15+6767A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561255 | ||||||
| chr4:78561555
|
T | C | 1 | a0001c0001t0002g0221 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.15+7067T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561555 | ||||||
| chr4:78561578
|
C | T | 4 | a0001c0001t0001g0289a0001c0001t0001g0299a0001c0001t0002g0310others(1): Show | 4 | HG02486.hp1 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+7090C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561578 | ||||||
| chr4:78561639
|
T | A | 3 | a0001c0001t0001g0093a0001c0001t0002g0092a0001c0001t0003g0094 | 3 | HG02155.hp1 NA18945.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.15+7151T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561639 | ||||||
| chr4:78561808
|
A | G | 2 | a0001c0001t0001g0280a0001c0001t0002g0281 | 2 | NA18951.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.15+7320A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561808 | ||||||
| chr4:78561828
|
A | G | 309 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(306): Show | 326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.15+7340A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561828 | ||||||
| chr4:78561950
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.15+7462A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561950 | ||||||
| chr4:78561965
|
A | G | 1 | a0001c0001t0003g0203 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.15+7477A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561965 | ||||||
| chr4:78562184
|
G | A | 71 | a0001c0001t0001g0075a0001c0001t0001g0133a0001c0001t0001g0169others(68): Show | 76 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.15+7696G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78562184 | ||||||
| chr4:78562227
|
G | GA | 218 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(215): Show | 232 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.15+7746dupA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78562227 | |||||
| chr4:78562281
|
A | G | 124 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(121): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.15+7793A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78562281 | ||||||
| chr4:78562398
|
G | C | 1 | a0001c0001t0003g0222 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.15+7910G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78562398 | ||||||
| chr4:78562438
|
T | A | 1 | a0004c0005t0003g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.15+7950T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78562438 | ||||||
| chr4:78562498
|
G | A | 2 | a0001c0002t0006g0300a0001c0011t0008g0074 | 2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.15+8010G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78562498 | ||||||
| chr4:78562704
|
T | C | 1 | a0001c0011t0008g0074 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.15+8216T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78562704 | ||||||
| chr4:78562716
|
T | C | 1 | a0001c0001t0002g0301 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.15+8228T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78562716 | ||||||
| chr4:78562717
|
G | A | 22 | a0001c0001t0001g0024a0001c0001t0002g0053a0001c0001t0002g0054others(19): Show | 23 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.15+8229G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78562717 | ||||||
| chr4:78562965
|
C | A | 1 | a0001c0001t0001g0095 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.15+8477C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78562965 | ||||||
| chr4:78563148
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.15+8660C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78563148 | ||||||
| chr4:78563162
|
A | G | 1 | a0001c0011t0008g0074 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.15+8674A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78563162 | ||||||
| chr4:78563238
|
G | A | 71 | a0001c0001t0001g0075a0001c0001t0001g0133a0001c0001t0001g0169others(68): Show | 76 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.15+8750G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78563238 | ||||||
| chr4:78563297
|
G | T | 3 | a0001c0001t0003g0135a0001c0001t0003g0136a0008c0010t0004g0157 | 3 | HG00735.hp1 HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.15+8809G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78563297 | ||||||
| chr4:78563333
|
A | G | 2 | a0001c0001t0004g0153a0001c0001t0007g0154 | 2 | HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.15+8845A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78563333 | ||||||
| chr4:78563463
|
G | GT | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | HG00280.hp2 HG01168.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.15+8975_15+8976ins others(1): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78563463 | ||||||
| chr4:78563506
|
AG | A | 135 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(132): Show | 144 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.15+9020delG | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78563506 | |||||
| chr4:78563526
|
ACGT | A | 215 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(212): Show | 229 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.15+9040_15+9042del others(3): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78563526 | |||||
| chr4:78563531
|
T | A | 215 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(212): Show | 229 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.15+9043T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78563531 | ||||||
| chr4:78563548
|
A | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0130a0001c0001t0001g0131others(1): Show | 5 | NA18978.hp2 NA18979.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+9060A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78563548 | ||||||
| chr4:78563564
|
G | A | 1 | a0001c0001t0002g0028 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.15+9076G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78563564 | ||||||
| chr4:78563731
|
G | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0289a0001c0001t0001g0299others(1): Show | 4 | HG02647.hp1 HG03041.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+9243G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78563731 | ||||||
| chr4:78564536
|
G | C | 1 | a0001c0001t0001g0213 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.16-8644G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78564536 | ||||||
| chr4:78564722
|
G | A | 122 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(119): Show | 131 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.16-8458G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78564722 | ||||||
| chr4:78564991
|
AT | A | 126 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(123): Show | 135 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.16-8169delT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78564991 | |||||
| chr4:78564991
|
ATT | A | 26 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0004g0076others(23): Show | 27 | HG00735.hp1 HG01891.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.16-8170_16-8169del others(2): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78564991 | |||||
| chr4:78564991
|
ATTT | A | 12 | a0001c0001t0001g0024a0001c0001t0002g0053a0001c0001t0004g0022others(9): Show | 12 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.16-8171_16-8169del others(3): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78564991 | |||||
| chr4:78565146
|
A | T | 1 | a0001c0001t0004g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.16-8034A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78565146 | ||||||
| chr4:78565178
|
G | A | 1 | a0001c0001t0002g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.16-8002G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78565178 | ||||||
| chr4:78565264
|
G | A | 5 | a0001c0001t0001g0283a0001c0001t0001g0289a0001c0001t0001g0299others(2): Show | 5 | HG02486.hp1 HG02647.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-7916G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78565264 | ||||||
| chr4:78565510
|
G | T | 3 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140 | 3 | HG00323.hp1 HG01106.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.16-7670G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78565510 | ||||||
| chr4:78565540
|
C | T | 2 | a0001c0001t0002g0053a0001c0001t0002g0054 | 2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.16-7640C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78565540 | ||||||
| chr4:78565610
|
C | T | 13 | a0001c0001t0001g0024a0001c0001t0002g0053a0001c0001t0002g0054others(10): Show | 13 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.16-7570C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78565610 | ||||||
| chr4:78565680
|
C | T | 1 | a0001c0001t0003g0113 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.16-7500C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78565680 | ||||||
| chr4:78565906
|
A | C | 216 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(213): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.16-7274A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78565906 | ||||||
| chr4:78566052
|
T | G | 10 | a0001c0001t0002g0301a0001c0001t0004g0147a0001c0001t0004g0148others(7): Show | 11 | HG02258.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.16-7128T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78566052 | ||||||
| chr4:78566054
|
A | G | 1 | a0001c0001t0001g0268 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.16-7126A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78566054 | ||||||
| chr4:78566156
|
T | A | 1 | a0001c0001t0002g0035 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.16-7024T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78566156 | ||||||
| chr4:78566440
|
A | AATACT | 209 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(206): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.16-6721_16-6717dup others(5): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78566440 | |||||
| chr4:78566440
|
A | AATACTAT others(3): Show |
6 | a0001c0002t0001g0063a0001c0002t0001g0064a0001c0002t0001g0065others(3): Show | 6 | HG02280.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.16-6726_16-6717dup others(10): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78566440 | |||||
| chr4:78566441
|
A | G | 3 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0002t0001g0077 | 3 | HG02572.hp1 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.16-6739A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78566441 | ||||||
| chr4:78566488
|
C | CA | 240 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(237): Show | 255 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.16-6678dupA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78566488 | |||||
| chr4:78566712
|
A | G | 3 | a0001c0001t0003g0135a0001c0001t0003g0136a0008c0010t0004g0157 | 3 | HG00735.hp1 HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.16-6468A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78566712 | ||||||
| chr4:78566847
|
A | T | 1 | a0008c0010t0004g0157 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.16-6333A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78566847 | ||||||
| chr4:78566901
|
A | T | 117 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(114): Show | 126 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.16-6279A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78566901 | ||||||
| chr4:78567036
|
C | T | 1 | a0001c0002t0006g0300 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.16-6144C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567036 | ||||||
| chr4:78567116
|
G | A | 211 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(208): Show | 225 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.16-6064G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567116 | ||||||
| chr4:78567257
|
T | C | 1 | a0001c0001t0002g0206 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.16-5923T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567257 | ||||||
| chr4:78567264
|
A | G | 2 | a0001c0001t0004g0147a0001c0001t0004g0148 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.16-5916A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567264 | ||||||
| chr4:78567306
|
A | T | 68 | a0001c0001t0001g0075a0001c0001t0001g0133a0001c0001t0001g0173others(65): Show | 73 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.16-5874A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567306 | ||||||
| chr4:78567330
|
C | G | 1 | a0001c0001t0002g0059 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16-5850C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567330 | ||||||
| chr4:78567359
|
G | A | 1 | a0001c0001t0003g0171 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.16-5821G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567359 | ||||||
| chr4:78567411
|
C | T | 1 | a0001c0001t0003g0214 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.16-5769C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567411 | ||||||
| chr4:78567472
|
G | A | 18 | a0001c0001t0001g0024a0001c0001t0002g0053a0001c0001t0004g0022others(15): Show | 18 | HG01884.hp1 HG02145.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.16-5708G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567472 | ||||||
| chr4:78567488
|
CAT | C | 7 | a0001c0001t0001g0024a0001c0001t0004g0022a0001c0001t0004g0060others(4): Show | 7 | HG02622.hp2 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.16-5691_16-5690del others(2): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567488 | ||||||
| chr4:78567564
|
A | G | 1 | a0001c0001t0001g0196 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.16-5616A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567564 | ||||||
| chr4:78567950
|
C | T | 1 | a0001c0001t0003g0195 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.16-5230C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567950 | ||||||
| chr4:78568000
|
C | G | 9 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0039others(6): Show | 9 | HG01891.hp1 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.16-5180C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78568000 | ||||||
| chr4:78568070
|
A | ATC | 8 | a0001c0001t0002g0062a0001c0001t0002g0301a0003c0004t0002g0072others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-5108_16-5107dup others(2): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78568070 | |||||
| chr4:78568395
|
G | A | 10 | a0001c0001t0001g0024a0001c0001t0002g0053a0001c0001t0002g0054others(7): Show | 10 | HG02145.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.16-4785G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78568395 | ||||||
| chr4:78568671
|
C | A | 1 | a0001c0002t0003g0050 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.16-4509C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78568671 | ||||||
| chr4:78568685
|
A | C | 1 | a0001c0001t0001g0034 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.16-4495A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78568685 | ||||||
| chr4:78568970
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.16-4210C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78568970 | ||||||
| chr4:78568985
|
T | A | 10 | a0001c0002t0001g0052a0001c0002t0001g0063a0001c0002t0001g0064others(7): Show | 10 | HG02109.hp2 HG02280.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.16-4195T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78568985 | ||||||
| chr4:78569042
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.16-4138C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78569042 | ||||||
| chr4:78569049
|
A | G | 8 | a0001c0001t0002g0062a0001c0001t0002g0301a0003c0004t0002g0072others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-4131A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78569049 | ||||||
| chr4:78569215
|
A | G | 1 | a0001c0001t0001g0268 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.16-3965A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78569215 | ||||||
| chr4:78569222
|
T | A | 5 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0004g0076others(2): Show | 5 | HG00735.hp1 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.16-3958T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78569222 | ||||||
| chr4:78569313
|
C | T | 7 | a0001c0001t0002g0062a0001c0001t0002g0301a0003c0004t0002g0072others(4): Show | 7 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-3867C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78569313 | ||||||
| chr4:78569314
|
G | A | 2 | a0001c0001t0001g0229a0001c0011t0008g0074 | 2 | HG01175.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.16-3866G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78569314 | ||||||
| chr4:78569711
|
C | T | 3 | a0001c0001t0001g0109a0001c0001t0001g0165a0008c0010t0004g0157 | 3 | HG01891.hp2 NA18944.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.16-3469C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78569711 | ||||||
| chr4:78569767
|
A | G | 1 | a0001c0001t0002g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16-3413A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78569767 | ||||||
| chr4:78570108
|
C | G | 22 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0039others(19): Show | 22 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.16-3072C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78570108 | ||||||
| chr4:78570162
|
A | G | 1 | a0001c0001t0002g0287 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.16-3018A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78570162 | ||||||
| chr4:78570697
|
T | C | 1 | a0001c0001t0004g0043 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.16-2483T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78570697 | ||||||
| chr4:78570754
|
T | C | 4 | a0003c0004t0002g0072a0003c0004t0004g0309a0003c0004t0006g0071others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-2426T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78570754 | ||||||
| chr4:78570772
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.16-2408T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78570772 | ||||||
| chr4:78570778
|
G | A | 1 | a0001c0001t0002g0310 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.16-2402G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78570778 | ||||||
| chr4:78571022
|
T | C | 1 | a0008c0010t0004g0157 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.16-2158T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78571022 | ||||||
| chr4:78571253
|
C | G | 1 | a0001c0001t0007g0154 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.16-1927C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78571253 | ||||||
| chr4:78571270
|
G | T | 4 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0004g0147others(1): Show | 4 | HG00735.hp1 HG02572.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-1910G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78571270 | ||||||
| chr4:78571299
|
C | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0130a0001c0001t0001g0201 | 4 | NA18979.hp1 NA18998.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-1881C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78571299 | ||||||
| chr4:78571496
|
G | C | 1 | a0001c0001t0002g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.16-1684G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78571496 | ||||||
| chr4:78571634
|
A | G | 1 | a0003c0004t0006g0073 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.16-1546A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78571634 | ||||||
| chr4:78571794
|
A | G | 8 | a0001c0001t0002g0062a0001c0001t0002g0301a0003c0004t0002g0072others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-1386A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78571794 | ||||||
| chr4:78572173
|
T | C | 1 | a0001c0001t0003g0214 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.16-1007T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78572173 | ||||||
| chr4:78572689
|
G | A | 94 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(91): Show | 100 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.16-491G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78572689 | ||||||
| chr4:78572690
|
G | C | 1 | a0001c0001t0001g0229 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.16-490G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78572690 | ||||||
| chr4:78572692
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.16-488C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78572692 | ||||||
| chr4:78572771
|
G | A | 1 | a0001c0001t0003g0214 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.16-409G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78572771 | ||||||
| chr4:78573153
|
A | G | 6 | a0001c0001t0001g0024a0001c0001t0004g0022a0001c0001t0004g0060others(3): Show | 6 | HG02622.hp2 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-27A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78573153 | ||||||
| chr4:78573276
|
T | C | 67 | a0001c0001t0001g0133a0001c0001t0001g0160a0001c0001t0001g0177others(64): Show | 72 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.103+9T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78573276 | ||||||
| chr4:78573291
|
T | G | 1 | a0001c0001t0003g0230 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.103+24T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78573291 | ||||||
| chr4:78573392
|
G | C | 4 | a0003c0004t0002g0072a0003c0004t0004g0309a0003c0004t0006g0071others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+125G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78573392 | ||||||
| chr4:78573511
|
C | T | 2 | a0001c0001t0002g0156a0001c0001t0002g0267 | 2 | HG00642.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.103+244C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78573511 | ||||||
| chr4:78573652
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.103+385G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78573652 | ||||||
| chr4:78573734
|
G | T | 1 | a0001c0001t0003g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.103+467G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78573734 | ||||||
| chr4:78573864
|
G | A | 1 | a0001c0001t0003g0176 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.103+597G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78573864 | ||||||
| chr4:78574027
|
T | A | 12 | a0001c0001t0001g0177a0001c0001t0001g0291a0001c0001t0002g0225others(9): Show | 13 | NA18952.hp2 NA18960.hp2 NA18968.hp1 others(10): Show |
intron_variant | MODIFIER | c.103+760T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78574027 | ||||||
| chr4:78574155
|
C | A | 228 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(225): Show | 240 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.103+888C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78574155 | ||||||
| chr4:78574802
|
A | T | 179 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(176): Show | 190 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.103+1535A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78574802 | ||||||
| chr4:78574904
|
C | T | 1 | a0001c0012t0001g0302 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.103+1637C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78574904 | ||||||
| chr4:78575014
|
C | A | 1 | a0001c0001t0002g0092 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.103+1747C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575014 | ||||||
| chr4:78575240
|
T | A | 1 | a0001c0001t0003g0079 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.103+1973T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575240 | ||||||
| chr4:78575325
|
G | A | 22 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0039others(19): Show | 22 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.103+2058G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575325 | ||||||
| chr4:78575334
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.103+2067G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575334 | ||||||
| chr4:78575399
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.103+2132G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575399 | ||||||
| chr4:78575443
|
C | T | 13 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0004g0076others(10): Show | 14 | HG00735.hp1 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.103+2176C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575443 | ||||||
| chr4:78575444
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.103+2177G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575444 | ||||||
| chr4:78575556
|
T | TG | 44 | a0001c0001t0001g0024a0001c0001t0002g0062a0001c0001t0002g0301others(41): Show | 45 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.103+2289_103+2290i others(3): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575556 | ||||||
| chr4:78575674
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.103+2407G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575674 | ||||||
| chr4:78575681
|
G | T | 6 | a0001c0001t0001g0024a0001c0001t0004g0022a0001c0001t0004g0060others(3): Show | 6 | HG02622.hp2 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.103+2414G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575681 | ||||||
| chr4:78575827
|
T | C | 1 | a0001c0001t0004g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.103+2560T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575827 | ||||||
| chr4:78576085
|
G | A | 2 | a0001c0001t0001g0308a0001c0001t0004g0043 | 2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.103+2818G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576085 | ||||||
| chr4:78576191
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.104-2836A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576191 | ||||||
| chr4:78576507
|
C | T | 9 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0096others(6): Show | 11 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.104-2520C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576507 | ||||||
| chr4:78576572
|
T | G | 1 | a0001c0001t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.104-2455T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576572 | ||||||
| chr4:78576575
|
A | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0220 | 2 | HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.104-2452A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576575 | ||||||
| chr4:78576583
|
C | A | 6 | a0001c0001t0001g0024a0001c0001t0004g0022a0001c0001t0004g0060others(3): Show | 6 | HG02622.hp2 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-2444C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576583 | ||||||
| chr4:78576598
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.104-2429G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576598 | ||||||
| chr4:78576631
|
T | A | 2 | a0001c0001t0003g0036a0001c0001t0007g0154 | 2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.104-2396T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576631 | ||||||
| chr4:78576713
|
C | T | 4 | a0001c0002t0006g0300a0001c0011t0008g0074a0002c0003t0006g0005others(1): Show | 5 | HG02258.hp1 HG02976.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-2314C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576713 | ||||||
| chr4:78576734
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.104-2293G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576734 | ||||||
| chr4:78576740
|
G | T | 4 | a0001c0002t0006g0300a0001c0011t0008g0074a0002c0003t0006g0005others(1): Show | 5 | HG02258.hp1 HG02976.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-2287G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576740 | ||||||
| chr4:78576793
|
G | A | 5 | a0001c0001t0001g0044a0001c0001t0003g0079a0001c0001t0003g0080others(2): Show | 5 | HG01109.hp2 HG03704.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-2234G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576793 | ||||||
| chr4:78577030
|
A | T | 7 | a0001c0001t0001g0111a0001c0001t0001g0202a0001c0001t0001g0213others(4): Show | 7 | HG00621.hp2 HG02056.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.104-1997A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78577030 | ||||||
| chr4:78577242
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.104-1785C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78577242 | ||||||
| chr4:78577267
|
T | G | 1 | a0001c0001t0001g0124 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.104-1760T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78577267 | ||||||
| chr4:78577367
|
A | G | 45 | a0001c0001t0001g0024a0001c0001t0002g0062a0001c0001t0002g0301others(42): Show | 46 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(43): Show |
intron_variant | MODIFIER | c.104-1660A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78577367 | ||||||
| chr4:78577814
|
G | A | 4 | a0001c0002t0006g0300a0001c0011t0008g0074a0002c0003t0006g0005others(1): Show | 5 | HG02258.hp1 HG02976.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-1213G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78577814 | ||||||
| chr4:78577934
|
C | T | 178 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(175): Show | 189 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.104-1093C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78577934 | ||||||
| chr4:78577968
|
T | A | 1 | a0008c0010t0004g0157 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.104-1059T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78577968 | ||||||
| chr4:78578000
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.104-1027C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578000 | ||||||
| chr4:78578105
|
C | T | 22 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0039others(19): Show | 22 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.104-922C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578105 | ||||||
| chr4:78578121
|
T | TA | 7 | a0001c0001t0001g0280a0001c0001t0002g0055a0001c0001t0002g0056others(4): Show | 7 | HG01243.hp2 HG02615.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.104-896dupA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578121 | |||||
| chr4:78578266
|
A | G | 1 | a0008c0010t0004g0157 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.104-761A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578266 | ||||||
| chr4:78578282
|
A | G | 41 | a0001c0001t0001g0024a0001c0001t0002g0062a0001c0001t0002g0301others(38): Show | 42 | HG00735.hp1 HG01891.hp1 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.104-745A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578282 | ||||||
| chr4:78578298
|
C | CGA | 9 | a0001c0001t0001g0024a0001c0001t0001g0125a0001c0001t0001g0277others(6): Show | 9 | HG02055.hp2 HG02615.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.104-698_104-697dup others(2): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
C | CGAGA | 13 | a0001c0001t0001g0114a0001c0001t0001g0122a0001c0001t0001g0194others(10): Show | 15 | HG00733.hp1 HG01175.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.104-700_104-697dup others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
C | CGAGAGA | 10 | a0001c0001t0001g0044a0001c0001t0001g0075a0001c0001t0001g0115others(7): Show | 10 | HG01070.hp2 HG01109.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.104-702_104-697dup others(6): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
C | CGAGAGAG others(1): Show |
10 | a0001c0001t0001g0021a0001c0001t0001g0081a0001c0001t0001g0116others(7): Show | 10 | HG00280.hp2 HG00673.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.104-704_104-697dup others(8): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
C | CGAGAGAG others(3): Show |
7 | a0001c0001t0001g0082a0001c0001t0001g0233a0001c0001t0001g0234others(4): Show | 7 | HG00140.hp2 HG00642.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.104-706_104-697dup others(10): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
C | CGAGAGAG others(5): Show |
24 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0025others(21): Show | 26 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.104-708_104-697dup others(12): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
C | CGAGAGAG others(7): Show |
16 | a0001c0001t0001g0129a0001c0001t0001g0174a0001c0001t0001g0219others(13): Show | 16 | HG01099.hp2 HG01175.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.104-710_104-697dup others(14): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
C | CGAGAGAG others(9): Show |
13 | a0001c0001t0001g0013a0001c0001t0001g0096a0001c0001t0001g0131others(10): Show | 14 | HG00408.hp2 HG02615.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.104-712_104-697dup others(16): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
C | CGAGAGAG others(11): Show |
21 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0014others(18): Show | 24 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.104-714_104-697dup others(18): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
C | CGAGAGAG others(13): Show |
4 | a0001c0001t0001g0045a0001c0001t0001g0213a0001c0001t0002g0310others(1): Show | 4 | HG02056.hp2 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-716_104-697dup others(20): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
C | CGAGAGAG others(15): Show |
4 | a0001c0001t0002g0205a0001c0001t0002g0207a0001c0001t0002g0208others(1): Show | 4 | HG01109.hp1 HG01167.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-718_104-697dup others(22): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
C | CGAGAGAG others(19): Show |
1 | a0001c0001t0005g0263 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.104-722_104-697dup others(26): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
C | CGAGAGCG others(3): Show |
1 | a0001c0001t0003g0135 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.104-724_104-723ins others(10): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
C | CGAGAGCG others(7): Show |
1 | a0001c0001t0003g0136 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.104-724_104-723ins others(14): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
C | CGAGAGCG others(11): Show |
1 | a0001c0001t0004g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.104-724_104-723ins others(18): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
C | CGAGAGTG others(5): Show |
6 | a0001c0001t0001g0177a0001c0001t0001g0291a0001c0001t0002g0225others(3): Show | 6 | HG04228.hp1 NA18952.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-724_104-723ins others(12): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
C | CGAGAGTG others(9): Show |
34 | a0001c0001t0001g0160a0001c0001t0001g0184a0001c0001t0001g0200others(31): Show | 38 | HG00323.hp1 HG00423.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.104-724_104-723ins others(16): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
C | CGAGAGTG others(11): Show |
7 | a0001c0001t0001g0133a0001c0001t0001g0196a0001c0001t0003g0018others(4): Show | 7 | HG02074.hp1 NA18612.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.104-724_104-723ins others(18): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
C | CGAGAGTG others(13): Show |
3 | a0001c0001t0003g0016a0001c0001t0003g0274a0001c0001t0003g0275 | 4 | NA18967.hp1 NA18970.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-724_104-723ins others(20): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
CGA | C | 6 | a0001c0002t0006g0300a0003c0004t0002g0072a0003c0004t0004g0309others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.104-698_104-697del others(2): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
CGAGA | C | 5 | a0001c0001t0002g0161a0001c0001t0004g0147a0001c0001t0004g0148others(2): Show | 6 | HG02258.hp1 HG02572.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-700_104-697del others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
CGAGAGAG others(3): Show |
C | 1 | a0001c0002t0003g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.104-706_104-697del others(10): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578298
|
CGAGAGAG others(5): Show |
C | 1 | a0001c0001t0003g0311 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.104-708_104-697del others(12): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | |||||
| chr4:78578300
|
A | AGAGC | 18 | a0001c0002t0001g0019a0001c0002t0001g0039a0001c0002t0001g0041others(15): Show | 18 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.104-724_104-723ins others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578300 | |||||
| chr4:78578302
|
A | T | 1 | a0001c0011t0008g0074 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.104-725A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578302 | ||||||
| chr4:78578304
|
A | C | 3 | a0001c0001t0002g0062a0001c0001t0002g0301a0001c0002t0003g0050 | 3 | HG02559.hp2 HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.104-723A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578304 | ||||||
| chr4:78578304
|
A | T | 4 | a0001c0001t0003g0112a0001c0001t0003g0140a0001c0001t0003g0192others(1): Show | 4 | HG00544.hp1 HG01106.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-723A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578304 | ||||||
| chr4:78578306
|
A | C | 1 | a0004c0005t0003g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.104-721A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578306 | ||||||
| chr4:78578308
|
A | C | 2 | a0001c0001t0004g0147a0001c0001t0004g0148 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.104-719A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578308 | ||||||
| chr4:78578314
|
A | C | 1 | a0001c0002t0003g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.104-713A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578314 | ||||||
| chr4:78578330
|
A | AGAGAGAG others(2): Show |
4 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0279others(1): Show | 4 | HG01168.hp2 HG01255.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-697_104-696ins others(9): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578330 | ||||||
| chr4:78578330
|
A | AGAGAGAG others(6): Show |
7 | a0001c0001t0001g0175a0001c0001t0001g0223a0001c0001t0001g0247others(4): Show | 7 | HG00408.hp1 HG00558.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.104-697_104-696ins others(13): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578330 | ||||||
| chr4:78578330
|
A | AGAGAGAG others(8): Show |
1 | a0001c0001t0001g0250 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.104-697_104-696ins others(15): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578330 | ||||||
| chr4:78578330
|
A | AGAGAGAG others(10): Show |
6 | a0001c0001t0001g0155a0001c0001t0001g0201a0001c0001t0003g0112others(3): Show | 6 | HG00544.hp1 HG01106.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-697_104-696ins others(17): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578330 | ||||||
| chr4:78578330
|
A | AGAGAGAG others(12): Show |
2 | a0001c0001t0001g0130a0001c0001t0001g0299 | 2 | HG06807.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.104-697_104-696ins others(19): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578330 | ||||||
| chr4:78578330
|
A | AGAGAGAG others(14): Show |
2 | a0001c0001t0001g0097a0001c0001t0002g0206 | 2 | HG01243.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.104-697_104-696ins others(21): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578330 | ||||||
| chr4:78578345
|
G | C | 1 | a0001c0001t0005g0259 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.104-682G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578345 | ||||||
| chr4:78578362
|
A | AGAGGGAG others(9): Show |
40 | a0001c0001t0001g0024a0001c0001t0002g0062a0001c0001t0003g0135others(37): Show | 41 | HG00735.hp1 HG01891.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.104-655_104-654ins others(16): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578362 | |||||
| chr4:78578467
|
G | T | 4 | a0003c0004t0002g0072a0003c0004t0004g0309a0003c0004t0006g0071others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-560G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578467 | ||||||
| chr4:78578473
|
G | T | 1 | a0001c0002t0003g0050 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.104-554G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578473 | ||||||
| chr4:78578533
|
G | A | 1 | a0001c0002t0001g0077 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.104-494G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578533 | ||||||
| chr4:78578702
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.104-325C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578702 | ||||||
| chr4:78578720
|
A | T | 1 | a0001c0001t0006g0057 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.104-307A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578720 | ||||||
| chr4:78578722
|
A | G | 10 | a0001c0001t0001g0024a0001c0001t0004g0022a0001c0001t0004g0060others(7): Show | 11 | HG02258.hp1 HG02622.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.104-305A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578722 | ||||||
| chr4:78578753
|
G | A | 22 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0039others(19): Show | 22 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.104-274G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578753 | ||||||
| chr4:78578768
|
A | C | 1 | a0008c0010t0004g0157 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.104-259A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578768 | ||||||
| chr4:78578825
|
CT | C | 41 | a0001c0001t0001g0024a0001c0001t0002g0062a0001c0001t0002g0183others(38): Show | 42 | HG00735.hp1 HG01891.hp1 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.104-193delT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578825 | |||||
| chr4:78578834
|
T | C | 178 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(175): Show | 189 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.104-193T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578834 | ||||||
| chr4:78578852
|
A | AAAAT | 34 | a0001c0001t0001g0045a0001c0001t0001g0082a0001c0001t0001g0084others(31): Show | 35 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.104-139_104-136dup others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578852 | |||||
| chr4:78578852
|
A | AAAATAAA others(1): Show |
70 | a0001c0001t0001g0160a0001c0001t0001g0177a0001c0001t0001g0184others(67): Show | 75 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.104-143_104-136dup others(8): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578852 | |||||
| chr4:78578852
|
A | AAAATAAA others(5): Show |
4 | a0001c0001t0001g0308a0001c0001t0002g0054a0001c0001t0004g0043others(1): Show | 4 | HG02717.hp1 HG02970.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-147_104-136dup others(12): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578852 | |||||
| chr4:78578852
|
A | AAAATAAA others(9): Show |
1 | a0001c0001t0005g0047 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.104-151_104-136dup others(16): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578852 | |||||
| chr4:78578852
|
AAAATAAA others(1): Show |
A | 31 | a0001c0001t0001g0024a0001c0001t0004g0022a0001c0001t0004g0060others(28): Show | 32 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.104-143_104-136del others(8): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578852 | |||||
| chr4:78579192
|
G | A | 6 | a0001c0001t0001g0024a0001c0001t0004g0022a0001c0001t0004g0060others(3): Show | 6 | HG02622.hp2 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+71G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579192 | ||||||
| chr4:78579366
|
C | A | 1 | a0001c0001t0001g0109 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.198+245C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579366 | ||||||
| chr4:78579367
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.198+246A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579367 | ||||||
| chr4:78579464
|
C | G | 22 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0039others(19): Show | 22 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.198+343C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579464 | ||||||
| chr4:78579508
|
G | A | 1 | a0001c0001t0001g0194 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.198+387G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579508 | ||||||
| chr4:78579723
|
G | A | 4 | a0003c0004t0002g0072a0003c0004t0004g0309a0003c0004t0006g0071others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+602G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579723 | ||||||
| chr4:78579754
|
C | T | 1 | a0001c0001t0003g0172 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.198+633C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579754 | ||||||
| chr4:78579868
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.198+747G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579868 | ||||||
| chr4:78579920
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.198+799G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579920 | ||||||
| chr4:78579931
|
C | A | 2 | a0001c0002t0006g0300a0001c0011t0008g0074 | 2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.198+810C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579931 | ||||||
| chr4:78579955
|
G | A | 1 | a0001c0001t0003g0112 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.198+834G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579955 | ||||||
| chr4:78580145
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.198+1024G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580145 | ||||||
| chr4:78580349
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.198+1228G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580349 | ||||||
| chr4:78580408
|
G | A | 4 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0004g0147others(1): Show | 4 | HG00735.hp1 HG02572.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+1287G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580408 | ||||||
| chr4:78580586
|
G | C | 23 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0039others(20): Show | 23 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.198+1465G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580586 | ||||||
| chr4:78580591
|
A | G | 1 | a0001c0001t0002g0163 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.198+1470A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580591 | ||||||
| chr4:78580600
|
A | G | 6 | a0001c0001t0002g0053a0001c0001t0002g0054a0002c0003t0004g0048others(3): Show | 7 | HG02145.hp2 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+1479A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580600 | ||||||
| chr4:78580705
|
C | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0130a0001c0001t0001g0131others(2): Show | 6 | NA18978.hp2 NA18979.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-1472C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580705 | ||||||
| chr4:78580866
|
A | G | 1 | a0001c0001t0002g0301 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.199-1311A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580866 | ||||||
| chr4:78580871
|
G | A | 48 | a0001c0001t0001g0024a0001c0001t0002g0053a0001c0001t0002g0054others(45): Show | 49 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(46): Show |
intron_variant | MODIFIER | c.199-1306G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580871 | ||||||
| chr4:78580888
|
A | T | 25 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0039others(22): Show | 25 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.199-1289A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580888 | ||||||
| chr4:78580928
|
T | G | 3 | a0001c0001t0002g0210a0001c0001t0004g0153a0002c0003t0004g0150 | 3 | HG02809.hp1 HG02895.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.199-1249T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580928 | ||||||
| chr4:78581278
|
C | T | 23 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0039others(20): Show | 23 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-899C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78581278 | ||||||
| chr4:78581287
|
G | A | 177 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(174): Show | 188 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.199-890G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78581287 | ||||||
| chr4:78581343
|
G | C | 1 | a0008c0010t0004g0157 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.199-834G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78581343 | ||||||
| chr4:78581403
|
G | A | 1 | a0001c0001t0004g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.199-774G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78581403 | ||||||
| chr4:78581415
|
A | G | 226 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(223): Show | 238 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.199-762A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78581415 | ||||||
| chr4:78581616
|
T | C | 1 | a0001c0002t0006g0300 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.199-561T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78581616 | ||||||
| chr4:78581818
|
T | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(98): Show | 107 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.199-359T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78581818 | ||||||
| chr4:78581875
|
A | G | 1 | a0001c0001t0003g0123 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.199-302A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78581875 | ||||||
| chr4:78581942
|
A | G | 23 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0039others(20): Show | 23 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-235A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78581942 | ||||||
| chr4:78582076
|
T | C | 191 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(188): Show | 203 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.199-101T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78582076 | ||||||
| chr4:78582416
|
G | A | 2 | a0001c0002t0001g0063a0001c0002t0001g0064 | 2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.312+126G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78582416 | ||||||
| chr4:78582497
|
T | C | 2 | a0001c0001t0004g0060a0001c0001t0004g0061 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.312+207T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78582497 | ||||||
| chr4:78582580
|
A | G | 9 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0004g0147others(6): Show | 9 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.312+290A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78582580 | ||||||
| chr4:78582635
|
A | T | 1 | a0001c0001t0001g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.312+345A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78582635 | ||||||
| chr4:78582784
|
A | G | 25 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0039others(22): Show | 25 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.312+494A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78582784 | ||||||
| chr4:78582967
|
G | A | 215 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(212): Show | 227 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.312+677G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78582967 | ||||||
| chr4:78583098
|
G | A | 4 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0004g0147others(1): Show | 4 | HG00735.hp1 HG02572.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+808G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583098 | ||||||
| chr4:78583158
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.312+868G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583158 | ||||||
| chr4:78583175
|
C | G | 1 | a0004c0005t0003g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.312+885C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583175 | ||||||
| chr4:78583182
|
TA | T | 224 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(221): Show | 236 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.312+902delA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 78583182 | |||||
| chr4:78583216
|
C | A | 2 | a0001c0001t0002g0062a0004c0005t0003g0070 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.312+926C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583216 | ||||||
| chr4:78583287
|
A | G | 1 | a0001c0001t0002g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.312+997A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583287 | ||||||
| chr4:78583462
|
A | C | 1 | a0002c0003t0004g0150 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.312+1172A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583462 | ||||||
| chr4:78583536
|
A | C | 2 | a0001c0002t0006g0300a0001c0011t0008g0074 | 2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.312+1246A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583536 | ||||||
| chr4:78583550
|
G | A | 1 | a0001c0001t0004g0288 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.312+1260G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583550 | ||||||
| chr4:78583563
|
A | G | 25 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0039others(22): Show | 25 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.312+1273A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583563 | ||||||
| chr4:78583613
|
G | GA | 7 | a0001c0001t0001g0251a0001c0001t0002g0087a0001c0001t0003g0009others(4): Show | 8 | HG00544.hp1 HG01952.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.312+1338dupA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 78583613 | |||||
| chr4:78583626
|
A | G | 25 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0039others(22): Show | 25 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.312+1336A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583626 | ||||||
| chr4:78583756
|
T | G | 4 | a0003c0004t0002g0072a0003c0004t0004g0309a0003c0004t0006g0071others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+1466T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583756 | ||||||
| chr4:78584064
|
G | A | 2 | a0001c0001t0003g0010a0001c0001t0003g0199 | 3 | NA18968.hp1 NA18978.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.312+1774G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584064 | ||||||
| chr4:78584111
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.312+1821A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584111 | ||||||
| chr4:78584131
|
C | T | 10 | a0001c0001t0002g0301a0001c0001t0003g0135a0001c0001t0003g0136others(7): Show | 10 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.312+1841C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584131 | ||||||
| chr4:78584152
|
G | T | 1 | a0001c0002t0001g0306 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.312+1862G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584152 | ||||||
| chr4:78584163
|
T | A | 9 | a0001c0002t0001g0052a0001c0002t0001g0063a0001c0002t0001g0064others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.312+1873T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584163 | ||||||
| chr4:78584412
|
G | A | 2 | a0001c0002t0006g0300a0001c0011t0008g0074 | 2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.313-1848G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584412 | ||||||
| chr4:78584420
|
C | T | 3 | a0001c0001t0002g0031a0001c0001t0002g0162a0001c0001t0002g0197 | 3 | HG00673.hp2 HG02056.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.313-1840C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584420 | ||||||
| chr4:78584427
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.313-1833C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584427 | ||||||
| chr4:78584431
|
C | T | 1 | a0001c0001t0003g0172 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.313-1829C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584431 | ||||||
| chr4:78584513
|
T | G | 1 | a0004c0005t0003g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.313-1747T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584513 | ||||||
| chr4:78584618
|
T | C | 216 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(213): Show | 228 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.313-1642T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584618 | ||||||
| chr4:78584730
|
T | C | 177 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(174): Show | 188 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.313-1530T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584730 | ||||||
| chr4:78584784
|
T | A | 25 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0039others(22): Show | 25 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.313-1476T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584784 | ||||||
| chr4:78584814
|
G | A | 14 | a0001c0001t0001g0024a0001c0001t0002g0062a0001c0001t0002g0301others(11): Show | 14 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.313-1446G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584814 | ||||||
| chr4:78584828
|
G | C | 1 | a0001c0002t0006g0300 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.313-1432G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584828 | ||||||
| chr4:78584842
|
C | T | 1 | a0001c0001t0003g0188 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.313-1418C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584842 | ||||||
| chr4:78585041
|
G | A | 1 | a0001c0001t0002g0054 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.313-1219G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78585041 | ||||||
| chr4:78585268
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0001g0165 | 2 | NA18944.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.313-992T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78585268 | ||||||
| chr4:78585269
|
C | A | 1 | a0001c0001t0002g0310 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.313-991C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78585269 | ||||||
| chr4:78585380
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.313-880A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78585380 | ||||||
| chr4:78585574
|
C | G | 2 | a0001c0002t0006g0300a0001c0011t0008g0074 | 2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.313-686C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78585574 | ||||||
| chr4:78585710
|
G | T | 224 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(221): Show | 236 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.313-550G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78585710 | ||||||
| chr4:78585761
|
A | G | 6 | a0001c0001t0001g0024a0001c0001t0004g0022a0001c0001t0004g0060others(3): Show | 6 | HG02622.hp2 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.313-499A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78585761 | ||||||
| chr4:78585809
|
A | T | 4 | a0003c0004t0002g0072a0003c0004t0004g0309a0003c0004t0006g0071others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-451A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78585809 | ||||||
| chr4:78585990
|
A | G | 1 | a0001c0001t0004g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.313-270A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78585990 | ||||||
| chr4:78586257
|
T | C | 3 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0101 | 3 | HG00140.hp1 HG01099.hp1 HG02257.hp2 |
splice_region_variant&intron_variant | LOW | c.313-3T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78586257 | ||||||
| chr4:78586431
|
C | T | 4 | a0002c0003t0004g0048a0002c0003t0004g0049a0002c0003t0006g0005others(1): Show | 5 | HG02145.hp2 HG02258.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.403+81C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78586431 | ||||||
| chr4:78586681
|
G | A | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00735.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.403+331G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78586681 | ||||||
| chr4:78586681
|
G | T | 5 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0088others(2): Show | 5 | HG00597.hp2 HG01928.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.403+331G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78586681 | ||||||
| chr4:78586956
|
C | T | 8 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0039others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.403+606C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78586956 | ||||||
| chr4:78587059
|
T | C | 1 | a0001c0001t0005g0047 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.403+709T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587059 | ||||||
| chr4:78587087
|
A | C | 181 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(178): Show | 193 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.403+737A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587087 | ||||||
| chr4:78587218
|
C | T | 177 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(174): Show | 188 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.403+868C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587218 | ||||||
| chr4:78587410
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.403+1060C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587410 | ||||||
| chr4:78587453
|
G | A | 177 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(174): Show | 188 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.403+1103G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587453 | ||||||
| chr4:78587505
|
C | T | 1 | a0004c0005t0003g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.403+1155C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587505 | ||||||
| chr4:78587650
|
G | A | 1 | a0001c0001t0003g0265 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.403+1300G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587650 | ||||||
| chr4:78587712
|
C | T | 8 | a0001c0001t0001g0122a0001c0001t0001g0194a0001c0001t0002g0007others(5): Show | 10 | HG00733.hp1 HG01070.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.403+1362C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587712 | ||||||
| chr4:78587732
|
C | A | 1 | a0001c0002t0006g0300 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.403+1382C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587732 | ||||||
| chr4:78587732
|
C | T | 199 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(196): Show | 211 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.403+1382C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587732 | ||||||
| chr4:78587818
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.403+1468G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587818 | ||||||
| chr4:78587821
|
C | T | 191 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(188): Show | 203 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.403+1471C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587821 | ||||||
| chr4:78587853
|
G | A | 1 | a0001c0001t0003g0112 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.403+1503G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587853 | ||||||
| chr4:78588107
|
T | C | 1 | a0001c0001t0002g0156 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.403+1757T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78588107 | ||||||
| chr4:78588220
|
C | A | 199 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(196): Show | 211 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.403+1870C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78588220 | ||||||
| chr4:78588669
|
A | G | 2 | a0001c0002t0006g0300a0001c0011t0008g0074 | 2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.403+2319A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78588669 | ||||||
| chr4:78588927
|
T | C | 1 | a0001c0001t0003g0222 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.403+2577T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78588927 | ||||||
| chr4:78588986
|
G | A | 23 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0039others(20): Show | 23 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.404-2558G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78588986 | ||||||
| chr4:78589103
|
C | T | 224 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(221): Show | 236 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.404-2441C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589103 | ||||||
| chr4:78589142
|
C | A | 1 | a0001c0001t0002g0159 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.404-2402C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589142 | ||||||
| chr4:78589182
|
C | T | 1 | a0001c0001t0003g0123 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.404-2362C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589182 | ||||||
| chr4:78589212
|
C | T | 1 | a0001c0002t0006g0300 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.404-2332C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589212 | ||||||
| chr4:78589213
|
A | G | 215 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(212): Show | 227 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.404-2331A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589213 | ||||||
| chr4:78589304
|
A | G | 213 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(210): Show | 225 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.404-2240A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589304 | ||||||
| chr4:78589310
|
C | T | 4 | a0001c0001t0001g0024a0001c0001t0004g0022a0001c0001t0005g0023others(1): Show | 4 | HG02886.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-2234C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589310 | ||||||
| chr4:78589324
|
A | G | 23 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0039others(20): Show | 23 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.404-2220A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589324 | ||||||
| chr4:78589343
|
G | T | 2 | a0001c0001t0001g0122a0001c0002t0001g0304 | 2 | HG02040.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.404-2201G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589343 | ||||||
| chr4:78589359
|
G | A | 1 | a0001c0002t0006g0300 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.404-2185G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589359 | ||||||
| chr4:78589417
|
A | G | 24 | a0001c0001t0002g0301a0001c0002t0001g0019a0001c0002t0001g0037others(21): Show | 24 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.404-2127A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589417 | ||||||
| chr4:78589517
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG00408.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.404-2027G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589517 | ||||||
| chr4:78589677
|
G | A | 2 | a0001c0002t0006g0300a0001c0011t0008g0074 | 2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.404-1867G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589677 | ||||||
| chr4:78589801
|
A | G | 1 | a0001c0001t0002g0301 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.404-1743A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589801 | ||||||
| chr4:78589819
|
T | C | 224 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(221): Show | 236 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.404-1725T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589819 | ||||||
| chr4:78589877
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.404-1667C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589877 | ||||||
| chr4:78589900
|
G | A | 24 | a0001c0001t0002g0301a0001c0002t0001g0019a0001c0002t0001g0037others(21): Show | 24 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.404-1644G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589900 | ||||||
| chr4:78590163
|
G | C | 2 | a0001c0002t0006g0300a0001c0011t0008g0074 | 2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.404-1381G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590163 | ||||||
| chr4:78590209
|
T | C | 196 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(193): Show | 208 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.404-1335T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590209 | ||||||
| chr4:78590319
|
T | C | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG02486.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-1225T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590319 | ||||||
| chr4:78590322
|
A | T | 2 | a0001c0001t0002g0062a0004c0005t0003g0070 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.404-1222A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590322 | ||||||
| chr4:78590346
|
A | G | 1 | a0008c0010t0004g0157 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.404-1198A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590346 | ||||||
| chr4:78590385
|
A | G | 4 | a0001c0001t0001g0024a0001c0001t0004g0022a0001c0001t0005g0023others(1): Show | 4 | HG02886.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-1159A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590385 | ||||||
| chr4:78590400
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.404-1144G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590400 | ||||||
| chr4:78590504
|
C | A | 1 | a0001c0001t0003g0170 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.404-1040C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590504 | ||||||
| chr4:78590667
|
G | A | 4 | a0003c0004t0002g0072a0003c0004t0004g0309a0003c0004t0006g0071others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.404-877G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590667 | ||||||
| chr4:78590762
|
T | A | 1 | a0001c0001t0003g0078 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.404-782T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590762 | ||||||
| chr4:78590777
|
T | TAAGATTA others(321): Show |
1 | a0001c0002t0001g0039 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.404-756_404-755ins others(328): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 78590777 | |||||
| chr4:78590777
|
T | TAAGATTA others(318): Show |
1 | a0001c0002t0001g0304 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.404-756_404-755ins others(325): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 78590777 | |||||
| chr4:78590777
|
T | TAAGATTA others(319): Show |
2 | a0001c0002t0003g0050a0001c0012t0001g0302 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.404-756_404-755ins others(326): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 78590777 | |||||
| chr4:78590777
|
T | TAAGATTA others(320): Show |
3 | a0001c0002t0003g0038a0001c0002t0004g0151a0001c0002t0006g0149 | 3 | HG01891.hp1 HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.404-756_404-755ins others(327): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 78590777 | |||||
| chr4:78590777
|
T | TAAGATTA others(321): Show |
11 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.404-756_404-755ins others(328): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 78590777 | |||||
| chr4:78590777
|
T | TAAGATTA others(322): Show |
3 | a0001c0002t0001g0063a0001c0002t0001g0066a0001c0002t0001g0077 | 3 | HG03471.hp2 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.404-756_404-755ins others(329): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 78590777 | |||||
| chr4:78590777
|
T | TAAGATTA others(323): Show |
2 | a0001c0002t0001g0065a0001c0002t0001g0305 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.404-756_404-755ins others(330): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 78590777 | |||||
| chr4:78590832
|
A | AAGCCACT others(2): Show |
6 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0041others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.404-712_404-711ins others(9): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590832 | ||||||
| chr4:78590833
|
G | A | 6 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0041others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.404-711G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590833 | ||||||
| chr4:78590835
|
A | G | 6 | a0001c0002t0001g0019a0001c0002t0001g0037a0001c0002t0001g0041others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.404-709A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590835 | ||||||
| chr4:78590916
|
T | A | 2 | a0001c0002t0006g0300a0001c0011t0008g0074 | 2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.404-628T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590916 | ||||||
| chr4:78590920
|
A | G | 220 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(217): Show | 232 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.404-624A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590920 | ||||||
| chr4:78590946
|
T | G | 181 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(178): Show | 193 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.404-598T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590946 | ||||||
| chr4:78591646
|
T | A | 176 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(173): Show | 187 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.483+23T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78591646 | ||||||
| chr4:78591702
|
C | G | 1 | a0001c0001t0002g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.483+79C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78591702 | ||||||
| chr4:78591853
|
T | C | 2 | a0001c0002t0006g0300a0001c0011t0008g0074 | 2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.483+230T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78591853 | ||||||
| chr4:78591962
|
G | A | 1 | a0008c0010t0004g0157 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.483+339G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78591962 | ||||||
| chr4:78591975
|
C | A | 1 | a0001c0011t0008g0074 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.483+352C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78591975 | ||||||
| chr4:78592061
|
A | G | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(130): Show | 140 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.483+438A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592061 | ||||||
| chr4:78592217
|
T | C | 214 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(211): Show | 226 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.483+594T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592217 | ||||||
| chr4:78592230
|
A | G | 1 | a0008c0010t0004g0157 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.483+607A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592230 | ||||||
| chr4:78592288
|
A | G | 5 | a0001c0001t0002g0301a0003c0004t0002g0072a0003c0004t0004g0309others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.483+665A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592288 | ||||||
| chr4:78592320
|
A | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.483+697A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592320 | ||||||
| chr4:78592410
|
C | T | 1 | a0001c0001t0002g0163 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.483+787C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592410 | ||||||
| chr4:78592428
|
G | A | 6 | a0001c0001t0004g0022a0001c0001t0004g0060a0001c0001t0004g0061others(3): Show | 6 | HG02622.hp2 HG02886.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.483+805G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592428 | ||||||
| chr4:78592453
|
A | C | 215 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(212): Show | 227 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.483+830A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592453 | ||||||
| chr4:78592539
|
A | G | 22 | a0001c0001t0001g0299a0001c0002t0001g0019a0001c0002t0001g0037others(19): Show | 22 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.483+916A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592539 | ||||||
| chr4:78592612
|
T | C | 3 | a0001c0001t0003g0079a0001c0001t0003g0080a0001c0001t0003g0083 | 3 | HG03704.hp2 HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.483+989T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592612 | ||||||
| chr4:78592820
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.483+1197A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592820 | ||||||
| chr4:78592859
|
G | A | 3 | a0001c0001t0003g0135a0001c0001t0003g0136a0008c0010t0004g0157 | 3 | HG00735.hp1 HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.483+1236G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592859 | ||||||
| chr4:78593020
|
A | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18979.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.483+1397A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593020 | ||||||
| chr4:78593040
|
G | A | 2 | a0001c0001t0002g0062a0004c0005t0003g0070 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.483+1417G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593040 | ||||||
| chr4:78593112
|
A | AACACAC | 3 | a0001c0001t0001g0013a0001c0001t0001g0233a0001c0001t0002g0264 | 4 | HG03710.hp1 NA18951.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+1489_483+1490i others(8): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593112 | ||||||
| chr4:78593113
|
C | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0233a0001c0001t0002g0264 | 4 | HG03710.hp1 NA18951.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+1490C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593113 | ||||||
| chr4:78593113
|
C | CCA | 32 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0045others(29): Show | 33 | HG00423.hp1 HG00597.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.483+1528_483+1529d others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593113 | |||||
| chr4:78593113
|
C | CCACA | 123 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0044others(120): Show | 128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.483+1526_483+1529d others(6): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593113 | |||||
| chr4:78593113
|
C | CCACACA | 23 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0012others(20): Show | 27 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.483+1524_483+1529d others(8): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593113 | |||||
| chr4:78593113
|
C | CCACACAC others(1): Show |
12 | a0001c0001t0001g0082a0001c0001t0001g0125a0001c0001t0001g0126others(9): Show | 12 | HG00140.hp2 HG01099.hp1 HG03688.hp1 others(9): Show |
intron_variant | MODIFIER | c.483+1522_483+1529d others(10): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593113 | |||||
| chr4:78593113
|
C | CCACACAC others(3): Show |
2 | a0001c0001t0001g0097a0001c0001t0002g0221 | 2 | HG02135.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.483+1520_483+1529d others(12): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593113 | |||||
| chr4:78593113
|
C | CCACACAC others(5): Show |
1 | a0001c0001t0001g0270 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.483+1518_483+1529d others(14): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593113 | |||||
| chr4:78593113
|
CCA | C | 61 | a0001c0001t0001g0160a0001c0001t0001g0177a0001c0001t0001g0184others(58): Show | 66 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.483+1528_483+1529d others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593113 | |||||
| chr4:78593113
|
CCACA | C | 17 | a0001c0001t0002g0027a0001c0001t0003g0135a0001c0001t0003g0136others(14): Show | 17 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.483+1526_483+1529d others(6): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593113 | |||||
| chr4:78593113
|
CCACACA | C | 6 | a0001c0001t0004g0022a0001c0001t0004g0060a0001c0001t0004g0061others(3): Show | 6 | HG02622.hp2 HG02886.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.483+1524_483+1529d others(8): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593113 | |||||
| chr4:78593151
|
A | C | 7 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0011t0008g0074others(4): Show | 7 | HG00735.hp1 HG01884.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+1528A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593151 | ||||||
| chr4:78593186
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.483+1563G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593186 | ||||||
| chr4:78593224
|
A | G | 1 | a0001c0001t0003g0276 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.483+1601A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593224 | ||||||
| chr4:78593250
|
T | A | 22 | a0001c0001t0001g0299a0001c0002t0001g0019a0001c0002t0001g0037others(19): Show | 22 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.483+1627T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593250 | ||||||
| chr4:78593251
|
G | GA | 22 | a0001c0001t0001g0299a0001c0002t0001g0019a0001c0002t0001g0037others(19): Show | 22 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.483+1628_483+1629i others(3): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593251 | ||||||
| chr4:78593263
|
T | C | 143 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(140): Show | 149 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.483+1640T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593263 | ||||||
| chr4:78593264
|
G | A | 1 | a0001c0001t0005g0261 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.483+1641G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593264 | ||||||
| chr4:78593340
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.483+1717T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593340 | ||||||
| chr4:78593400
|
T | C | 30 | a0001c0001t0001g0299a0001c0001t0004g0022a0001c0001t0004g0060others(27): Show | 30 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.483+1777T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593400 | ||||||
| chr4:78593449
|
G | A | 6 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0003g0079others(3): Show | 6 | HG01109.hp2 HG02559.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.483+1826G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593449 | ||||||
| chr4:78593454
|
A | G | 1 | a0004c0005t0003g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.483+1831A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593454 | ||||||
| chr4:78593612
|
C | T | 30 | a0001c0001t0001g0299a0001c0001t0004g0022a0001c0001t0004g0060others(27): Show | 30 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.484-1769C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593612 | ||||||
| chr4:78593625
|
C | CATT | 6 | a0001c0001t0002g0106a0001c0001t0002g0143a0001c0001t0002g0206others(3): Show | 6 | HG01106.hp1 HG01192.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.484-1731_484-1729d others(5): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593625 | |||||
| chr4:78593625
|
C | CATTATTA others(2): Show |
23 | a0001c0001t0001g0299a0001c0002t0001g0019a0001c0002t0001g0037others(20): Show | 23 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.484-1737_484-1729d others(11): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593625 | |||||
| chr4:78593625
|
C | CATTATTA others(14): Show |
5 | a0002c0003t0004g0048a0002c0003t0004g0049a0002c0003t0004g0150others(2): Show | 6 | HG02145.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.484-1749_484-1729d others(23): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593625 | |||||
| chr4:78593763
|
A | G | 21 | a0001c0001t0001g0299a0001c0002t0001g0019a0001c0002t0001g0037others(18): Show | 21 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.484-1618A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593763 | ||||||
| chr4:78593774
|
C | G | 70 | a0001c0001t0001g0160a0001c0001t0001g0177a0001c0001t0001g0184others(67): Show | 75 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.484-1607C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593774 | ||||||
| chr4:78593795
|
T | C | 30 | a0001c0001t0001g0299a0001c0001t0004g0022a0001c0001t0004g0060others(27): Show | 30 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.484-1586T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593795 | ||||||
| chr4:78593798
|
A | G | 40 | a0001c0001t0001g0299a0001c0001t0003g0135a0001c0001t0003g0136others(37): Show | 40 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.484-1583A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593798 | ||||||
| chr4:78593803
|
A | AT | 22 | a0001c0001t0001g0133a0001c0001t0001g0146a0001c0001t0001g0165others(19): Show | 23 | HG00597.hp2 HG01168.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.484-1552dupT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593803 | |||||
| chr4:78593803
|
A | ATT | 15 | a0001c0001t0002g0266a0001c0002t0001g0019a0001c0002t0001g0037others(12): Show | 15 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.484-1553_484-1552d others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593803 | |||||
| chr4:78593803
|
AT | A | 115 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(112): Show | 121 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.484-1552delT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593803 | |||||
| chr4:78593803
|
ATT | A | 68 | a0001c0001t0001g0093a0001c0001t0001g0126a0001c0001t0001g0160others(65): Show | 73 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.484-1553_484-1552d others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593803 | |||||
| chr4:78593803
|
ATTTTTTT others(6): Show |
A | 5 | a0001c0002t0004g0151a0003c0004t0002g0072a0003c0004t0004g0309others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.484-1564_484-1552d others(15): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593803 | |||||
| chr4:78593835
|
G | A | 1 | a0001c0001t0003g0104 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.484-1546G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593835 | ||||||
| chr4:78594159
|
TCAGG | T | 30 | a0001c0001t0001g0299a0001c0001t0004g0022a0001c0001t0004g0060others(27): Show | 30 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.484-1216_484-1213d others(6): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78594159 | |||||
| chr4:78594211
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.484-1170G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78594211 | ||||||
| chr4:78594314
|
G | GT | 218 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(215): Show | 230 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.484-1064dupT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78594314 | |||||
| chr4:78594462
|
C | A | 1 | a0001c0001t0001g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.484-919C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78594462 | ||||||
| chr4:78594469
|
C | G | 2 | a0001c0002t0006g0300a0004c0005t0003g0070 | 2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.484-912C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78594469 | ||||||
| chr4:78594496
|
A | C | 2 | a0001c0002t0006g0300a0004c0005t0003g0070 | 2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.484-885A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78594496 | ||||||
| chr4:78594556
|
A | G | 7 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0011t0008g0074others(4): Show | 7 | HG00735.hp1 HG01884.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.484-825A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78594556 | ||||||
| chr4:78594570
|
A | G | 218 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(215): Show | 230 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.484-811A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78594570 | ||||||
| chr4:78594739
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.484-642G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78594739 | ||||||
| chr4:78594851
|
G | A | 2 | a0001c0001t0002g0310a0004c0005t0003g0051 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.484-530G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78594851 | ||||||
| chr4:78595045
|
G | A | 2 | a0001c0001t0004g0043a0001c0001t0005g0047 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.484-336G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78595045 | ||||||
| chr4:78595051
|
G | A | 30 | a0001c0001t0001g0299a0001c0001t0004g0022a0001c0001t0004g0060others(27): Show | 30 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.484-330G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78595051 | ||||||
| chr4:78595130
|
A | C | 30 | a0001c0001t0001g0299a0001c0001t0004g0022a0001c0001t0004g0060others(27): Show | 30 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.484-251A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78595130 | ||||||
| chr4:78595141
|
A | AATATAT | 7 | a0001c0001t0004g0022a0001c0001t0004g0060a0001c0001t0004g0061others(4): Show | 7 | HG01891.hp2 HG02622.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.484-231_484-226dup others(6): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78595141 | |||||
| chr4:78595163
|
C | T | 10 | a0001c0001t0001g0299a0001c0002t0001g0019a0001c0002t0001g0037others(7): Show | 10 | HG02145.hp1 HG02723.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.484-218C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78595163 | ||||||
| chr4:78595212
|
C | A | 2 | a0001c0002t0001g0304a0001c0002t0006g0149 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.484-169C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78595212 | ||||||
| chr4:78595227
|
G | T | 23 | a0001c0001t0001g0299a0001c0002t0001g0019a0001c0002t0001g0037others(20): Show | 23 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.484-154G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78595227 | ||||||
| chr4:78595233
|
C | T | 1 | a0003c0004t0002g0072 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.484-148C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78595233 | ||||||
| chr4:78595273
|
C | G | 1 | a0001c0001t0002g0085 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.484-108C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78595273 | ||||||
| chr4:78595291
|
A | G | 4 | a0003c0004t0002g0072a0003c0004t0004g0309a0003c0004t0006g0071others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-90A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78595291 | ||||||
| chr4:78595536
|
T | TTTTC | 21 | a0001c0001t0001g0299a0001c0002t0001g0019a0001c0002t0001g0037others(18): Show | 21 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.540+103_540+106dup others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr4 | 78595536 | |||||
| chr4:78595540
|
C | CT | 5 | a0001c0001t0003g0179a0001c0002t0001g0304a0001c0002t0006g0149others(2): Show | 6 | HG01891.hp1 HG02258.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+116dupT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr4 | 78595540 | |||||
| chr4:78595540
|
C | CTTTTTT | 7 | a0001c0001t0004g0022a0001c0001t0004g0060a0001c0001t0004g0061others(4): Show | 7 | HG01891.hp2 HG02622.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.540+111_540+116dup others(6): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr4 | 78595540 | |||||
| chr4:78595540
|
CT | C | 7 | a0001c0001t0001g0045a0001c0001t0001g0308a0001c0001t0004g0043others(4): Show | 7 | HG01884.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+116delT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr4 | 78595540 | |||||
| chr4:78595900
|
A | T | 7 | a0001c0001t0004g0022a0001c0001t0004g0060a0001c0001t0004g0061others(4): Show | 7 | HG01891.hp2 HG02622.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.634+13A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78595900 | ||||||
| chr4:78595956
|
A | G | 7 | a0001c0001t0004g0022a0001c0001t0004g0060a0001c0001t0004g0061others(4): Show | 7 | HG01891.hp2 HG02622.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.634+69A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78595956 | ||||||
| chr4:78596152
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.634+265G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78596152 | ||||||
| chr4:78596152
|
G | T | 1 | a0001c0002t0001g0039 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.634+265G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78596152 | ||||||
| chr4:78596359
|
T | C | 1 | a0001c0002t0004g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.634+472T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78596359 | ||||||
| chr4:78596360
|
C | T | 23 | a0001c0001t0001g0299a0001c0002t0001g0019a0001c0002t0001g0037others(20): Show | 23 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.634+473C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78596360 | ||||||
| chr4:78596389
|
G | T | 1 | a0001c0012t0001g0302 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.634+502G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78596389 | ||||||
| chr4:78596403
|
T | C | 39 | a0001c0001t0001g0299a0001c0001t0003g0135a0001c0001t0003g0136others(36): Show | 39 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.634+516T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78596403 | ||||||
| chr4:78596461
|
T | C | 30 | a0001c0001t0001g0299a0001c0001t0004g0022a0001c0001t0004g0060others(27): Show | 30 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.634+574T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78596461 | ||||||
| chr4:78596620
|
G | A | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG02486.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.635-699G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78596620 | ||||||
| chr4:78596839
|
A | G | 1 | a0001c0001t0005g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.635-480A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78596839 | ||||||
| chr4:78597058
|
A | G | 7 | a0001c0001t0004g0022a0001c0001t0004g0060a0001c0001t0004g0061others(4): Show | 7 | HG01891.hp2 HG02622.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.635-261A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78597058 | ||||||
| chr4:78597140
|
T | C | 12 | a0001c0001t0004g0022a0001c0001t0004g0060a0001c0001t0004g0061others(9): Show | 13 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.635-179T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78597140 | ||||||
| chr4:78597242
|
A | G | 1 | a0001c0001t0005g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.635-77A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78597242 | ||||||
| chr4:78597283
|
C | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0096others(6): Show | 11 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.635-36C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78597283 | ||||||
| chr4:78597284
|
G | A | 2 | a0001c0002t0001g0304a0001c0002t0006g0149 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.635-35G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78597284 | ||||||
| chr4:78597425
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.730+11G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78597425 | ||||||
| chr4:78597499
|
CT | C | 2 | a0002c0003t0006g0005a0002c0003t0006g0137 | 3 | HG02258.hp1 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.730+86delT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78597499 | ||||||
| chr4:78597693
|
G | C | 23 | a0001c0001t0001g0299a0001c0002t0001g0019a0001c0002t0001g0037others(20): Show | 23 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.730+279G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78597693 | ||||||
| chr4:78597733
|
C | T | 35 | a0001c0001t0001g0299a0001c0001t0004g0022a0001c0001t0004g0060others(32): Show | 36 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(33): Show |
intron_variant | MODIFIER | c.730+319C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78597733 | ||||||
| chr4:78597814
|
A | G | 1 | a0001c0002t0006g0149 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.730+400A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78597814 | ||||||
| chr4:78597831
|
C | T | 1 | a0001c0001t0003g0190 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.730+417C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78597831 | ||||||
| chr4:78597983
|
C | T | 6 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0088others(3): Show | 6 | HG00597.hp2 HG01928.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.730+569C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78597983 | ||||||
| chr4:78598046
|
G | A | 1 | a0001c0001t0002g0281 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.730+632G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598046 | ||||||
| chr4:78598054
|
A | G | 14 | a0001c0001t0004g0022a0001c0001t0004g0060a0001c0001t0004g0061others(11): Show | 15 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.730+640A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598054 | ||||||
| chr4:78598070
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0090a0001c0001t0001g0091others(5): Show | 9 | HG00558.hp2 NA18948.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.730+656C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598070 | ||||||
| chr4:78598071
|
G | A | 2 | a0001c0002t0006g0300a0004c0005t0003g0070 | 2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.730+657G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598071 | ||||||
| chr4:78598148
|
T | C | 2 | a0001c0002t0001g0067a0001c0002t0001g0069 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.730+734T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598148 | ||||||
| chr4:78598178
|
A | G | 1 | a0001c0001t0001g0245 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.730+764A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598178 | ||||||
| chr4:78598179
|
C | CCA | 15 | a0001c0001t0002g0031a0001c0001t0002g0062a0001c0001t0002g0162others(12): Show | 16 | HG00673.hp2 HG02056.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.730+792_730+793dup others(2): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 78598179 | |||||
| chr4:78598179
|
C | CCACACAC others(3): Show |
4 | a0003c0004t0002g0072a0003c0004t0004g0309a0003c0004t0006g0071others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.730+784_730+793dup others(10): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 78598179 | |||||
| chr4:78598179
|
C | CCACACAC others(5): Show |
3 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0011t0008g0074 | 3 | HG00735.hp1 HG02622.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.730+782_730+793dup others(12): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 78598179 | |||||
| chr4:78598292
|
C | CT | 23 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0004g0022others(20): Show | 24 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.730+890dupT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 78598292 | |||||
| chr4:78598334
|
C | G | 1 | a0001c0001t0003g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.730+920C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598334 | ||||||
| chr4:78598397
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.730+983C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598397 | ||||||
| chr4:78598480
|
G | A | 1 | a0001c0001t0002g0159 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.730+1066G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598480 | ||||||
| chr4:78598500
|
C | A | 218 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(215): Show | 230 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.730+1086C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598500 | ||||||
| chr4:78598544
|
CT | C | 23 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0004g0022others(20): Show | 24 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.730+1139delT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 78598544 | |||||
| chr4:78598594
|
T | C | 16 | a0001c0001t0004g0022a0001c0001t0004g0060a0001c0001t0004g0061others(13): Show | 17 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.730+1180T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598594 | ||||||
| chr4:78598600
|
C | T | 3 | a0001c0001t0001g0245a0001c0001t0001g0253a0001c0001t0001g0256 | 3 | NA18999.hp1 NA19065.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.730+1186C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598600 | ||||||
| chr4:78598625
|
C | T | 2 | a0001c0001t0003g0036a0001c0001t0007g0154 | 2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.730+1211C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598625 | ||||||
| chr4:78598689
|
G | A | 1 | a0001c0002t0004g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.730+1275G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598689 | ||||||
| chr4:78598783
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.730+1369G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598783 | ||||||
| chr4:78598834
|
CT | C | 3 | a0001c0001t0004g0022a0001c0001t0005g0023a0001c0001t0005g0046 | 3 | HG02886.hp2 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.730+1421delT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598834 | ||||||
| chr4:78598901
|
C | T | 3 | a0001c0001t0002g0030a0001c0001t0002g0035a0001c0001t0002g0163 | 3 | HG02074.hp2 HG02135.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.730+1487C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598901 | ||||||
| chr4:78599012
|
A | G | 2 | a0001c0002t0006g0300a0004c0005t0003g0070 | 2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.730+1598A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599012 | ||||||
| chr4:78599046
|
C | A | 1 | a0001c0002t0004g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.730+1632C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599046 | ||||||
| chr4:78599160
|
C | T | 44 | a0001c0001t0001g0299a0001c0001t0003g0135a0001c0001t0003g0136others(41): Show | 45 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.730+1746C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599160 | ||||||
| chr4:78599161
|
T | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(98): Show | 107 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.730+1747T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599161 | ||||||
| chr4:78599178
|
A | G | 9 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0207others(6): Show | 9 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.730+1764A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599178 | ||||||
| chr4:78599221
|
A | G | 2 | a0001c0002t0006g0300a0004c0005t0003g0070 | 2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.730+1807A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599221 | ||||||
| chr4:78599235
|
C | T | 1 | a0001c0012t0001g0302 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.730+1821C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599235 | ||||||
| chr4:78599249
|
G | T | 1 | a0001c0001t0001g0241 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.730+1835G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599249 | ||||||
| chr4:78599394
|
C | T | 11 | a0001c0001t0004g0022a0001c0001t0004g0060a0001c0001t0004g0061others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.730+1980C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599394 | ||||||
| chr4:78599553
|
C | G | 5 | a0002c0003t0004g0048a0002c0003t0004g0049a0002c0003t0004g0150others(2): Show | 6 | HG02145.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.731-1957C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599553 | ||||||
| chr4:78599624
|
T | A | 5 | a0001c0001t0001g0044a0001c0001t0003g0079a0001c0001t0003g0080others(2): Show | 5 | HG01109.hp2 HG03704.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.731-1886T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599624 | ||||||
| chr4:78599656
|
G | A | 6 | a0001c0002t0001g0304a0001c0002t0006g0149a0001c0002t0006g0300others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.731-1854G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599656 | ||||||
| chr4:78599744
|
A | T | 43 | a0001c0001t0001g0299a0001c0001t0003g0079a0001c0001t0003g0080others(40): Show | 44 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(41): Show |
intron_variant | MODIFIER | c.731-1766A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599744 | ||||||
| chr4:78599808
|
C | T | 9 | a0001c0002t0001g0052a0001c0002t0001g0063a0001c0002t0001g0064others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.731-1702C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599808 | ||||||
| chr4:78599943
|
T | C | 11 | a0001c0001t0003g0168a0001c0001t0003g0181a0001c0001t0003g0187others(8): Show | 11 | HG02280.hp2 HG02622.hp2 HG03579.hp1 others(8): Show |
intron_variant | MODIFIER | c.731-1567T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599943 | ||||||
| chr4:78600031
|
C | T | 2 | a0001c0001t0002g0015a0001c0001t0002g0020 | 3 | HG01952.hp2 HG01981.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.731-1479C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78600031 | ||||||
| chr4:78600046
|
G | T | 53 | a0001c0001t0001g0160a0001c0001t0001g0177a0001c0001t0001g0196others(50): Show | 58 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.731-1464G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78600046 | ||||||
| chr4:78600274
|
G | A | 69 | a0001c0001t0001g0160a0001c0001t0001g0258a0001c0001t0002g0015others(66): Show | 75 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.731-1236G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78600274 | ||||||
| chr4:78600482
|
A | G | 1 | a0001c0001t0001g0269 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.731-1028A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78600482 | ||||||
| chr4:78600671
|
G | A | 2 | a0001c0001t0004g0060a0001c0001t0004g0061 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.731-839G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78600671 | ||||||
| chr4:78600748
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.731-762C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78600748 | ||||||
| chr4:78600825
|
T | G | 1 | a0001c0001t0001g0254 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.731-685T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78600825 | ||||||
| chr4:78600921
|
G | T | 3 | a0001c0002t0006g0300a0003c0004t0006g0071a0003c0004t0006g0073 | 3 | HG02280.hp2 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.731-589G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78600921 | ||||||
| chr4:78600936
|
AT | A | 11 | a0001c0001t0002g0027a0001c0001t0003g0036a0001c0001t0003g0079others(8): Show | 11 | HG00735.hp1 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.731-564delT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 78600936 | |||||
| chr4:78600967
|
A | G | 7 | a0001c0001t0006g0057a0001c0002t0006g0300a0002c0003t0006g0005others(4): Show | 8 | HG01891.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.731-543A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78600967 | ||||||
| chr4:78600997
|
A | C | 7 | a0001c0001t0006g0057a0001c0002t0006g0300a0002c0003t0006g0005others(4): Show | 8 | HG01891.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.731-513A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78600997 | ||||||
| chr4:78601054
|
T | C | 7 | a0001c0001t0006g0057a0001c0002t0006g0300a0002c0003t0006g0005others(4): Show | 8 | HG01891.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.731-456T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78601054 | ||||||
| chr4:78601057
|
C | T | 1 | a0001c0006t0001g0252 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.731-453C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78601057 | ||||||
| chr4:78601085
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.731-425G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78601085 | ||||||
| chr4:78601132
|
A | G | 4 | a0001c0001t0001g0280a0001c0001t0002g0017a0001c0001t0002g0221others(1): Show | 5 | HG01358.hp2 HG01934.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-378A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78601132 | ||||||
| chr4:78601360
|
C | A | 1 | a0003c0004t0004g0309 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.731-150C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78601360 | ||||||
| chr4:78601370
|
A | C | 2 | a0001c0001t0003g0171a0001c0001t0003g0227 | 2 | NA18939.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.731-140A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78601370 | ||||||
| chr4:78601415
|
C | T | 3 | a0001c0002t0004g0151a0004c0005t0003g0051a0004c0005t0003g0070 | 3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.731-95C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78601415 | ||||||
| chr4:78601444
|
T | C | 28 | a0001c0001t0001g0045a0001c0001t0001g0289a0001c0001t0001g0299others(25): Show | 28 | HG00735.hp1 HG01884.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.731-66T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78601444 | ||||||
| chr4:78601454
|
T | C | 1 | a0001c0001t0001g0224 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.731-56T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78601454 | ||||||
| chr4:78601491
|
T | C | 7 | a0001c0001t0006g0057a0001c0002t0006g0300a0002c0003t0006g0005others(4): Show | 8 | HG01891.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.731-19T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78601491 | ||||||
| chr4:78601844
|
C | G | 3 | a0001c0001t0004g0288a0002c0003t0004g0048a0002c0003t0004g0049 | 3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.789+276C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78601844 | ||||||
| chr4:78601864
|
A | T | 1 | a0001c0001t0005g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.789+296A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78601864 | ||||||
| chr4:78601995
|
C | T | 7 | a0001c0001t0006g0057a0001c0002t0006g0300a0002c0003t0006g0005others(4): Show | 8 | HG01891.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.789+427C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78601995 | ||||||
| chr4:78602013
|
C | T | 1 | a0001c0001t0004g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.789+445C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602013 | ||||||
| chr4:78602097
|
G | A | 1 | a0002c0003t0006g0137 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.789+529G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602097 | ||||||
| chr4:78602175
|
G | A | 3 | a0001c0002t0004g0151a0004c0005t0003g0051a0004c0005t0003g0070 | 3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.789+607G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602175 | ||||||
| chr4:78602239
|
C | CA | 27 | a0001c0001t0001g0045a0001c0001t0001g0146a0001c0001t0001g0244others(24): Show | 27 | HG00323.hp2 HG00735.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.789+690dupA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 78602239 | |||||
| chr4:78602239
|
C | CAA | 10 | a0001c0001t0001g0289a0001c0001t0001g0299a0001c0001t0001g0308others(7): Show | 10 | HG02280.hp1 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.789+689_789+690dup others(2): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 78602239 | |||||
| chr4:78602239
|
CA | C | 13 | a0001c0001t0001g0095a0001c0001t0001g0105a0001c0001t0001g0175others(10): Show | 13 | HG00558.hp1 HG02145.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.789+690delA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 78602239 | |||||
| chr4:78602442
|
A | G | 6 | a0001c0001t0006g0057a0001c0002t0006g0300a0002c0003t0006g0005others(3): Show | 7 | HG02258.hp1 HG02280.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.789+874A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602442 | ||||||
| chr4:78602541
|
G | T | 1 | a0001c0001t0003g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+973G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602541 | ||||||
| chr4:78602543
|
T | C | 1 | a0001c0001t0003g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+975T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602543 | ||||||
| chr4:78602544
|
G | C | 1 | a0001c0001t0003g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+976G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602544 | ||||||
| chr4:78602547
|
T | G | 1 | a0001c0001t0003g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+979T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602547 | ||||||
| chr4:78602548
|
T | A | 1 | a0001c0001t0003g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+980T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602548 | ||||||
| chr4:78602562
|
G | C | 1 | a0001c0001t0003g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+994G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602562 | ||||||
| chr4:78602563
|
A | C | 1 | a0001c0001t0003g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+995A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602563 | ||||||
| chr4:78602568
|
G | A | 25 | a0001c0001t0001g0045a0001c0001t0001g0173a0001c0001t0001g0215others(22): Show | 25 | HG00735.hp1 HG01884.hp2 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.789+1000G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602568 | ||||||
| chr4:78602589
|
T | G | 1 | a0001c0001t0003g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1021T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602589 | ||||||
| chr4:78602590
|
G | C | 1 | a0001c0001t0003g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1022G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602590 | ||||||
| chr4:78602592
|
CTTTACTG others(29): Show |
C | 1 | a0001c0001t0003g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1025_789+1060d others(38): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602592 | ||||||
| chr4:78602602
|
A | C | 1 | a0001c0001t0001g0255 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.789+1034A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602602 | ||||||
| chr4:78602630
|
C | T | 1 | a0001c0001t0003g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1062C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602630 | ||||||
| chr4:78602634
|
T | C | 1 | a0001c0001t0003g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1066T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602634 | ||||||
| chr4:78602635
|
T | G | 1 | a0001c0001t0003g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1067T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602635 | ||||||
| chr4:78602636
|
A | C | 1 | a0001c0001t0003g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1068A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602636 | ||||||
| chr4:78602642
|
A | C | 1 | a0001c0001t0003g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1074A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602642 | ||||||
| chr4:78602643
|
G | C | 1 | a0001c0001t0003g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1075G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602643 | ||||||
| chr4:78602645
|
C | G | 1 | a0001c0001t0003g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1077C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602645 | ||||||
| chr4:78602646
|
C | A | 1 | a0001c0001t0003g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1078C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602646 | ||||||
| chr4:78602655
|
T | A | 1 | a0001c0001t0003g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1087T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602655 | ||||||
| chr4:78602669
|
T | C | 1 | a0001c0001t0003g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1101T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602669 | ||||||
| chr4:78602768
|
C | A | 4 | a0001c0001t0004g0288a0002c0003t0004g0048a0002c0003t0004g0049others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.789+1200C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602768 | ||||||
| chr4:78602828
|
T | C | 7 | a0001c0001t0006g0057a0001c0002t0006g0300a0002c0003t0006g0005others(4): Show | 8 | HG01891.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.789+1260T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602828 | ||||||
| chr4:78603023
|
C | T | 2 | a0001c0001t0005g0023a0001c0001t0005g0046 | 2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.790-1254C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603023 | ||||||
| chr4:78603030
|
T | G | 1 | a0001c0002t0004g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.790-1247T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603030 | ||||||
| chr4:78603035
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.790-1242G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603035 | ||||||
| chr4:78603037
|
G | T | 1 | a0003c0004t0002g0072 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.790-1240G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603037 | ||||||
| chr4:78603104
|
C | G | 1 | a0001c0001t0001g0253 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.790-1173C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603104 | ||||||
| chr4:78603203
|
A | G | 1 | a0001c0001t0003g0170 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.790-1074A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603203 | ||||||
| chr4:78603230
|
G | T | 38 | a0001c0001t0001g0045a0001c0001t0001g0289a0001c0001t0001g0299others(35): Show | 39 | HG00735.hp1 HG01884.hp2 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.790-1047G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603230 | ||||||
| chr4:78603266
|
C | T | 229 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(226): Show | 241 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.790-1011C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603266 | ||||||
| chr4:78603377
|
A | G | 1 | a0001c0001t0001g0012 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.790-900A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603377 | ||||||
| chr4:78603548
|
A | G | 1 | a0008c0010t0004g0157 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.790-729A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603548 | ||||||
| chr4:78603631
|
G | A | 1 | a0001c0001t0003g0227 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.790-646G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603631 | ||||||
| chr4:78603744
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.790-533C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603744 | ||||||
| chr4:78603868
|
C | G | 19 | a0001c0001t0001g0045a0001c0001t0002g0027a0001c0001t0003g0036others(16): Show | 19 | HG00735.hp1 HG01884.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.790-409C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603868 | ||||||
| chr4:78603959
|
T | G | 3 | a0001c0001t0006g0057a0002c0003t0006g0005a0002c0003t0006g0137 | 4 | HG02258.hp1 HG03041.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-318T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603959 | ||||||
| chr4:78603991
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.790-286C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603991 | ||||||
| chr4:78604083
|
A | G | 6 | a0001c0001t0006g0057a0001c0002t0006g0300a0002c0003t0006g0005others(3): Show | 7 | HG02258.hp1 HG02280.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.790-194A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78604083 | ||||||
| chr4:78604095
|
T | C | 1 | a0001c0002t0004g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.790-182T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78604095 | ||||||
| chr4:78604250
|
G | A | 75 | a0001c0001t0001g0160a0001c0001t0002g0143a0001c0001t0002g0205others(72): Show | 81 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.790-27G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78604250 | ||||||
| chr4:78604430
|
A | ATTTT | 18 | a0001c0001t0002g0027a0001c0001t0003g0036a0001c0001t0003g0079others(15): Show | 18 | HG00735.hp1 HG01884.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.912+32_912+35dupTT others(2): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 78604430 | |||||
| chr4:78604431
|
T | C | 1 | a0001c0002t0004g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.912+32T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78604431 | ||||||
| chr4:78604436
|
CCCT | C | 18 | a0001c0001t0002g0027a0001c0001t0003g0036a0001c0001t0003g0079others(15): Show | 18 | HG00735.hp1 HG01884.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.912+38_912+40delCC others(1): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78604436 | ||||||
| chr4:78604514
|
A | G | 9 | a0001c0001t0001g0289a0001c0001t0001g0299a0001c0001t0001g0308others(6): Show | 9 | HG02280.hp1 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.912+115A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78604514 | ||||||
| chr4:78604562
|
C | T | 119 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(116): Show | 125 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.912+163C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78604562 | ||||||
| chr4:78604656
|
T | C | 6 | a0001c0001t0006g0057a0001c0002t0006g0300a0002c0003t0006g0005others(3): Show | 7 | HG02258.hp1 HG02280.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.912+257T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78604656 | ||||||
| chr4:78604705
|
C | T | 1 | a0001c0002t0004g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.912+306C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78604705 | ||||||
| chr4:78604824
|
T | C | 1 | a0008c0010t0004g0157 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.912+425T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78604824 | ||||||
| chr4:78604844
|
G | C | 1 | a0001c0001t0001g0111 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.912+445G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78604844 | ||||||
| chr4:78604892
|
G | A | 75 | a0001c0001t0001g0160a0001c0001t0002g0143a0001c0001t0002g0205others(72): Show | 81 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.912+493G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78604892 | ||||||
| chr4:78604955
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.912+556G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78604955 | ||||||
| chr4:78605149
|
T | C | 9 | a0001c0001t0001g0289a0001c0001t0001g0299a0001c0001t0001g0308others(6): Show | 9 | HG02280.hp1 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.912+750T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78605149 | ||||||
| chr4:78605258
|
C | T | 1 | a0001c0001t0003g0292 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.912+859C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78605258 | ||||||
| chr4:78605278
|
AG | A | 68 | a0001c0001t0001g0160a0001c0001t0002g0143a0001c0001t0002g0205others(65): Show | 73 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.912+881delG | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 78605278 | |||||
| chr4:78605345
|
A | G | 18 | a0001c0001t0002g0027a0001c0001t0003g0036a0001c0001t0003g0079others(15): Show | 18 | HG00735.hp1 HG01884.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.912+946A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78605345 | ||||||
| chr4:78605363
|
A | G | 76 | a0001c0001t0001g0160a0001c0001t0002g0143a0001c0001t0002g0205others(73): Show | 82 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.912+964A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78605363 | ||||||
| chr4:78605484
|
G | C | 89 | a0001c0001t0001g0160a0001c0001t0001g0289a0001c0001t0001g0299others(86): Show | 95 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.912+1085G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78605484 | ||||||
| chr4:78605787
|
A | T | 14 | a0001c0001t0001g0289a0001c0001t0001g0299a0001c0001t0001g0308others(11): Show | 14 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.912+1388A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78605787 | ||||||
| chr4:78605814
|
C | G | 111 | a0001c0001t0001g0160a0001c0001t0001g0289a0001c0001t0001g0299others(108): Show | 117 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.912+1415C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78605814 | ||||||
| chr4:78605855
|
G | A | 240 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(237): Show | 252 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.912+1456G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78605855 | ||||||
| chr4:78605930
|
G | A | 1 | a0008c0010t0004g0157 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.912+1531G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78605930 | ||||||
| chr4:78606118
|
C | T | 230 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(227): Show | 242 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.912+1719C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78606118 | ||||||
| chr4:78606236
|
G | T | 4 | a0001c0001t0004g0288a0002c0003t0004g0048a0002c0003t0004g0049others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.912+1837G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78606236 | ||||||
| chr4:78606390
|
T | A | 2 | a0001c0001t0004g0147a0001c0001t0004g0148 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.912+1991T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78606390 | ||||||
| chr4:78606529
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0121 | 3 | HG00733.hp2 HG00735.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.912+2130T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78606529 | ||||||
| chr4:78606566
|
C | T | 4 | a0001c0001t0001g0220a0001c0001t0001g0234a0001c0001t0001g0246others(1): Show | 4 | HG00642.hp2 HG01070.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.912+2167C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78606566 | ||||||
| chr4:78606675
|
T | TTGAA | 3 | a0001c0001t0001g0012a0001c0001t0001g0194a0001c0001t0001g0244 | 4 | HG01099.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.912+2297_912+2300d others(6): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 78606675 | |||||
| chr4:78606722
|
A | T | 3 | a0001c0001t0006g0057a0002c0003t0006g0005a0002c0003t0006g0137 | 4 | HG02258.hp1 HG03041.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.912+2323A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78606722 | ||||||
| chr4:78606794
|
AT | A | 202 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(199): Show | 213 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.912+2396delT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78606794 | ||||||
| chr4:78606872
|
C | A | 4 | a0001c0001t0006g0057a0001c0002t0006g0149a0002c0003t0006g0005others(1): Show | 5 | HG01891.hp1 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.912+2473C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78606872 | ||||||
| chr4:78607188
|
A | G | 27 | a0001c0001t0004g0022a0001c0001t0004g0043a0001c0001t0004g0060others(24): Show | 28 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.912+2789A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78607188 | ||||||
| chr4:78607388
|
AC | A | 6 | a0001c0001t0002g0011a0001c0001t0002g0033a0001c0001t0002g0161others(3): Show | 7 | HG00280.hp1 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.913-2666delC | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 78607388 | |||||
| chr4:78607462
|
AAG | A | 7 | a0001c0001t0006g0057a0001c0002t0006g0149a0001c0002t0006g0300others(4): Show | 8 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.913-2592_913-2591d others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 78607462 | |||||
| chr4:78607517
|
A | T | 72 | a0001c0001t0002g0143a0001c0001t0003g0002a0001c0001t0003g0009others(69): Show | 77 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.913-2539A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78607517 | ||||||
| chr4:78607644
|
CAT | C | 3 | a0001c0002t0006g0300a0003c0004t0006g0071a0003c0004t0006g0073 | 3 | HG02280.hp2 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.913-2410_913-2409d others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 78607644 | |||||
| chr4:78607659
|
G | A | 129 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(126): Show | 135 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.913-2397G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78607659 | ||||||
| chr4:78607687
|
A | G | 2 | a0004c0005t0003g0051a0004c0005t0003g0070 | 2 | HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.913-2369A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78607687 | ||||||
| chr4:78607735
|
T | C | 4 | a0001c0001t0006g0057a0001c0002t0006g0149a0002c0003t0006g0005others(1): Show | 5 | HG01891.hp1 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.913-2321T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78607735 | ||||||
| chr4:78607779
|
G | T | 1 | a0001c0001t0003g0275 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.913-2277G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78607779 | ||||||
| chr4:78607803
|
G | T | 72 | a0001c0001t0002g0143a0001c0001t0003g0002a0001c0001t0003g0009others(69): Show | 77 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.913-2253G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78607803 | ||||||
| chr4:78607817
|
C | T | 2 | a0001c0001t0004g0060a0001c0001t0004g0061 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.913-2239C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78607817 | ||||||
| chr4:78607982
|
T | C | 1 | a0001c0001t0005g0047 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.913-2074T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78607982 | ||||||
| chr4:78608051
|
C | A | 1 | a0001c0001t0002g0108 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.913-2005C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608051 | ||||||
| chr4:78608052
|
G | A | 129 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(126): Show | 135 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.913-2004G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608052 | ||||||
| chr4:78608136
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.913-1920G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608136 | ||||||
| chr4:78608260
|
G | A | 7 | a0001c0001t0006g0057a0001c0002t0006g0149a0001c0002t0006g0300others(4): Show | 8 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.913-1796G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608260 | ||||||
| chr4:78608476
|
C | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(125): Show | 134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.913-1580C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608476 | ||||||
| chr4:78608609
|
G | C | 1 | a0008c0010t0004g0157 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.913-1447G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608609 | ||||||
| chr4:78608687
|
G | A | 7 | a0001c0001t0004g0288a0001c0002t0003g0038a0002c0003t0004g0048others(4): Show | 7 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.913-1369G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608687 | ||||||
| chr4:78608736
|
G | A | 7 | a0001c0001t0006g0057a0001c0002t0006g0149a0001c0002t0006g0300others(4): Show | 8 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.913-1320G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608736 | ||||||
| chr4:78608746
|
C | A | 1 | a0001c0001t0002g0310 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.913-1310C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608746 | ||||||
| chr4:78608757
|
G | A | 7 | a0001c0001t0006g0057a0001c0002t0006g0149a0001c0002t0006g0300others(4): Show | 8 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.913-1299G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608757 | ||||||
| chr4:78608850
|
A | T | 1 | a0008c0010t0004g0157 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.913-1206A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608850 | ||||||
| chr4:78608907
|
C | T | 1 | a0001c0001t0006g0057 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.913-1149C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608907 | ||||||
| chr4:78608998
|
T | C | 1 | a0001c0001t0002g0161 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.913-1058T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608998 | ||||||
| chr4:78609028
|
A | G | 1 | a0001c0001t0001g0216 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.913-1028A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609028 | ||||||
| chr4:78609051
|
C | T | 10 | a0001c0001t0004g0022a0001c0001t0004g0043a0001c0001t0004g0060others(7): Show | 10 | HG02572.hp1 HG02622.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.913-1005C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609051 | ||||||
| chr4:78609126
|
G | T | 87 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(84): Show | 93 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.913-930G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609126 | ||||||
| chr4:78609367
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.913-689C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609367 | ||||||
| chr4:78609431
|
A | G | 2 | a0001c0002t0001g0067a0001c0002t0001g0069 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.913-625A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609431 | ||||||
| chr4:78609434
|
C | A | 1 | a0001c0001t0001g0155 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.913-622C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609434 | ||||||
| chr4:78609437
|
T | G | 1 | a0001c0002t0004g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.913-619T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609437 | ||||||
| chr4:78609578
|
C | T | 150 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(147): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.913-478C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609578 | ||||||
| chr4:78609581
|
G | A | 1 | a0001c0001t0004g0043 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.913-475G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609581 | ||||||
| chr4:78609706
|
C | T | 3 | a0001c0002t0006g0300a0003c0004t0006g0071a0003c0004t0006g0073 | 3 | HG02280.hp2 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.913-350C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609706 | ||||||
| chr4:78609884
|
G | A | 138 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(135): Show | 145 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.913-172G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609884 | ||||||
| chr4:78609904
|
A | C | 73 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(70): Show | 78 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.913-152A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609904 | ||||||
| chr4:78609924
|
T | C | 4 | a0001c0001t0004g0288a0002c0003t0004g0048a0002c0003t0004g0049others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.913-132T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609924 | ||||||
| chr4:78610032
|
C | T | 138 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(135): Show | 145 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.913-24C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78610032 | ||||||
| chr4:78610048
|
C | T | 76 | a0001c0001t0003g0002a0001c0001t0003g0009a0001c0001t0003g0010others(73): Show | 81 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
splice_region_variant&intron_variant | LOW | c.913-8C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78610048 |