Search by Gene
| geneid | 91283 |
|---|---|
| ensemblid | ENSG00000066697.15 |
| hgncid | 23370 |
| symbol | MSANTD3 |
| name | Myb/SANT DNA binding domain containing 3 |
| refseq_nuc | NM_080655.3 |
| refseq_prot | NP_542386.1 |
| ensembl_nuc | ENST00000395067.7 |
| ensembl_prot | ENSP00000378506.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 100427143 |
| end | 100451734 |
| strand | + |
| ver | v1.2 |
| region | chr9:100427143-100451734 |
| region5000 | chr9:100422143-100456734 |
| regionname0 | MSANTD3_chr9_100427143_100451734 |
| regionname5000 | MSANTD3_chr9_100422143_100456734 |
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 | 275 | 326 | 90 | 55 | 125 | 12 | 42 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0002 | 0/0 | 275 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0003 | 0/0 | 275 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | 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 | 1/0 | 828 | 302 | 87 | 44 | 124 | 7 | 39 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| c0002 | 0/1 | 828 | 23 | 3 | 11 | 0 | 5 | 3 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| c0003 | 0/0 | 828 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| c0004 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| c0005 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | 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 | 0/0 | 1052 | 149 | 36 | 23 | 71 | 3 | 16 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| t0002 | 0/0 | 1052 | 55 | 6 | 4 | 35 | 0 | 10 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| t0003 | 1/0 | 1053 | 53 | 15 | 8 | 19 | 2 | 8 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| t0004 | 0/1 | 1051 | 25 | 4 | 12 | 0 | 5 | 3 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| t0005 | 0/0 | 1051 | 12 | 12 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| t0006 | 0/0 | 1053 | 9 | 0 | 4 | 0 | 2 | 3 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| t0007 | 0/0 | 1052 | 7 | 7 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| t0008 | 0/0 | 1051 | 3 | 3 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| t0009 | 0/0 | 1051 | 2 | 1 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| t0010 | 0/0 | 1052 | 2 | 0 | 0 | 0 | 0 | 2 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| t0011 | 0/0 | 1052 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| t0012 | 0/0 | 1052 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| t0013 | 0/0 | 1052 | 2 | 0 | 2 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| t0014 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| t0015 | 0/0 | 1052 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| t0016 | 0/0 | 1053 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| t0017 | 0/0 | 1051 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| t0018 | 0/0 | 1053 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | 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 | 0/0 | 26 | 0 | 4 | 15 | 2 | 5 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0002 | 0/0 | 14 | 3 | 0 | 10 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0003 | 0/1 | 8 | 1 | 2 | 0 | 3 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0004 | 0/0 | 7 | 0 | 0 | 3 | 1 | 3 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0005 | 0/0 | 7 | 1 | 2 | 4 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0007 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0011 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0014 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0016 | 0/0 | 3 | 1 | 0 | 1 | 1 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0017 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0020 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0028 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| 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 | 1/0 | 302 | 87 | 44 | 124 | 7 | 39 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/1 | 23 | 3 | 11 | 0 | 5 | 3 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0002c0003 | a0002 | c0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0003c0005 | a0003 | c0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | 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 | 0/0 | 149 | 36 | 23 | 71 | 3 | 16 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 53 | 6 | 4 | 33 | 0 | 10 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 1/0 | 53 | 15 | 8 | 19 | 2 | 8 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 12 | 12 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 8 | 0 | 3 | 0 | 2 | 3 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0001t0011 | a0001 | c0001 | t0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0001t0016 | a0001 | c0001 | t0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0001t0017 | a0001 | c0001 | t0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0001t0018 | a0001 | c0001 | t0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0002t0004 | a0001 | c0002 | t0004 | 0/1 | 22 | 3 | 10 | 0 | 5 | 3 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0002t0015 | a0001 | c0002 | t0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0001c0004t0002 | a0001 | c0004 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0002c0003t0006 | a0002 | c0003 | t0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | copy fasta |
| a0003c0005t0002 | a0003 | c0005 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 20 | 0 | 1 | 13 | 1 | 5 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0011 | a0001 | c0001 | t0001 | g0011 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 3 | 1 | 0 | 1 | 1 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0037 | a0001 | c0001 | t0001 | g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0115 | a0001 | c0001 | t0001 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0183 | a0001 | c0001 | t0001 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0186 | a0001 | c0001 | t0001 | g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0001g0209 | a0001 | c0001 | t0001 | g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0002 | a0001 | c0001 | t0002 | g0002 | 0/0 | 13 | 3 | 0 | 9 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0019 | a0001 | c0001 | t0002 | g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0020 | a0001 | c0001 | t0002 | g0020 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0021 | a0001 | c0001 | t0002 | g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0038 | a0001 | c0001 | t0002 | g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0039 | a0001 | c0001 | t0002 | g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0070 | a0001 | c0001 | t0002 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0180 | a0001 | c0001 | t0002 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0181 | a0001 | c0001 | t0002 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0182 | a0001 | c0001 | t0002 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0184 | a0001 | c0001 | t0002 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0185 | a0001 | c0001 | t0002 | g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0187 | a0001 | c0001 | t0002 | g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0188 | a0001 | c0001 | t0002 | g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0189 | a0001 | c0001 | t0002 | g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0190 | a0001 | c0001 | t0002 | g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0191 | a0001 | c0001 | t0002 | g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0192 | a0001 | c0001 | t0002 | g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0194 | a0001 | c0001 | t0002 | g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0195 | a0001 | c0001 | t0002 | g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0196 | a0001 | c0001 | t0002 | g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0197 | a0001 | c0001 | t0002 | g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0198 | a0001 | c0001 | t0002 | g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0199 | a0001 | c0001 | t0002 | g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0200 | a0001 | c0001 | t0002 | g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0201 | a0001 | c0001 | t0002 | g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0202 | a0001 | c0001 | t0002 | g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0203 | a0001 | c0001 | t0002 | g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0204 | a0001 | c0001 | t0002 | g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0205 | a0001 | c0001 | t0002 | g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0206 | a0001 | c0001 | t0002 | g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0207 | a0001 | c0001 | t0002 | g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0002g0208 | a0001 | c0001 | t0002 | g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0001 | a0001 | c0001 | t0003 | g0001 | 0/0 | 6 | 0 | 3 | 2 | 1 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0004 | a0001 | c0001 | t0003 | g0004 | 0/0 | 7 | 0 | 0 | 3 | 1 | 3 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0005 | a0001 | c0001 | t0003 | g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0008 | a0001 | c0001 | t0003 | g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0013 | a0001 | c0001 | t0003 | g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0018 | a0001 | c0001 | t0003 | g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0025 | a0001 | c0001 | t0003 | g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0026 | a0001 | c0001 | t0003 | g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0027 | a0001 | c0001 | t0003 | g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0031 | a0001 | c0001 | t0003 | g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0041 | a0001 | c0001 | t0003 | g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0063 | a0001 | c0001 | t0003 | g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0067 | a0001 | c0001 | t0003 | g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0068 | a0001 | c0001 | t0003 | g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0073 | a0001 | c0001 | t0003 | g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0074 | a0001 | c0001 | t0003 | g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0075 | a0001 | c0001 | t0003 | g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0076 | a0001 | c0001 | t0003 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0079 | a0001 | c0001 | t0003 | g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0091 | a0001 | c0001 | t0003 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0092 | a0001 | c0001 | t0003 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0094 | a0001 | c0001 | t0003 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0096 | a0001 | c0001 | t0003 | g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0097 | a0001 | c0001 | t0003 | g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0108 | a0001 | c0001 | t0003 | g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0113 | a0001 | c0001 | t0003 | g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0114 | a0001 | c0001 | t0003 | g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0118 | a0001 | c0001 | t0003 | g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0119 | a0001 | c0001 | t0003 | g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0125 | a0001 | c0001 | t0003 | g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0129 | a0001 | c0001 | t0003 | g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0141 | a0001 | c0001 | t0003 | g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0142 | a0001 | c0001 | t0003 | g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0148 | a0001 | c0001 | t0003 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0157 | a0001 | c0001 | t0003 | g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0158 | a0001 | c0001 | t0003 | g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0003g0164 | a0001 | c0001 | t0003 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0004g0169 | a0001 | c0001 | t0004 | g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0004g0170 | a0001 | c0001 | t0004 | g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0004g0172 | a0001 | c0001 | t0004 | g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0005g0012 | a0001 | c0001 | t0005 | g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0005g0023 | a0001 | c0001 | t0005 | g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0005g0024 | a0001 | c0001 | t0005 | g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0005g0047 | a0001 | c0001 | t0005 | g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0005g0048 | a0001 | c0001 | t0005 | g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0005g0049 | a0001 | c0001 | t0005 | g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0005g0050 | a0001 | c0001 | t0005 | g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0005g0051 | a0001 | c0001 | t0005 | g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0006g0017 | a0001 | c0001 | t0006 | g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0006g0066 | a0001 | c0001 | t0006 | g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0006g0123 | a0001 | c0001 | t0006 | g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0006g0131 | a0001 | c0001 | t0006 | g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0006g0133 | a0001 | c0001 | t0006 | g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0006g0134 | a0001 | c0001 | t0006 | g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0006g0145 | a0001 | c0001 | t0006 | g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0007g0006 | a0001 | c0001 | t0007 | g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0007g0062 | a0001 | c0001 | t0007 | g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0008g0055 | a0001 | c0001 | t0008 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0008g0056 | a0001 | c0001 | t0008 | g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0008g0057 | a0001 | c0001 | t0008 | g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0009g0060 | a0001 | c0001 | t0009 | g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0009g0061 | a0001 | c0001 | t0009 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0010g0040 | a0001 | c0001 | t0010 | g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0011g0210 | a0001 | c0001 | t0011 | g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0011g0211 | a0001 | c0001 | t0011 | g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0012g0013 | a0001 | c0001 | t0012 | g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0012g0104 | a0001 | c0001 | t0012 | g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0013g0034 | a0001 | c0001 | t0013 | g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0013g0160 | a0001 | c0001 | t0013 | g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0014g0058 | a0001 | c0001 | t0014 | g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0016g0002 | a0001 | c0001 | t0016 | g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0017g0111 | a0001 | c0001 | t0017 | g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0001t0018g0017 | a0001 | c0001 | t0018 | g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0002t0004g0003 | a0001 | c0002 | t0004 | g0003 | 0/1 | 8 | 1 | 2 | 0 | 3 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0002t0004g0007 | a0001 | c0002 | t0004 | g0007 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0002t0004g0168 | a0001 | c0002 | t0004 | g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0002t0004g0171 | a0001 | c0002 | t0004 | g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0002t0004g0173 | a0001 | c0002 | t0004 | g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0002t0004g0174 | a0001 | c0002 | t0004 | g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0002t0004g0175 | a0001 | c0002 | t0004 | g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0002t0004g0176 | a0001 | c0002 | t0004 | g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0002t0004g0177 | a0001 | c0002 | t0004 | g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0002t0004g0178 | a0001 | c0002 | t0004 | g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0002t0004g0179 | a0001 | c0002 | t0004 | g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0002t0015g0167 | a0001 | c0002 | t0015 | g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0001c0004t0002g0069 | a0001 | c0004 | t0002 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0002c0003t0006g0065 | a0002 | c0003 | t0006 | g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| a0003c0005t0002g0193 | a0003 | c0005 | t0002 | g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0004 | g0003 | EUR | GBR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | GBR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00140 | hp1 | a0001 | c0002 | t0004 | g0003 | EUR | GBR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | GBR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00642 | hp1 | a0001 | c0001 | t0018 | g0017 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00733 | hp1 | a0001 | c0001 | t0009 | g0060 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00735 | hp2 | a0001 | c0002 | t0004 | g0171 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00738 | hp1 | a0001 | c0001 | t0006 | g0134 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00738 | hp2 | a0001 | c0002 | t0004 | g0007 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0145 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0142 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01069 | hp1 | a0001 | c0002 | t0004 | g0178 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01071 | hp1 | a0001 | c0002 | t0004 | g0007 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0170 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0141 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01099 | hp2 | a0001 | c0001 | t0013 | g0160 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01167 | hp2 | a0001 | c0002 | t0004 | g0177 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01169 | hp2 | a0001 | c0002 | t0015 | g0167 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01192 | hp1 | a0001 | c0001 | t0013 | g0034 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01192 | hp2 | a0001 | c0002 | t0004 | g0173 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01243 | hp1 | a0001 | c0002 | t0004 | g0003 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0123 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0096 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0169 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01361 | hp2 | a0001 | c0002 | t0004 | g0174 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0017 | EUR | IBS | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01516 | hp2 | a0001 | c0002 | t0004 | g0003 | EUR | IBS | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0017 | EUR | IBS | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0047 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01975 | hp2 | a0001 | c0002 | t0004 | g0007 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02055 | hp1 | a0001 | c0002 | t0004 | g0179 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CDX | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CDX | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CDX | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0051 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02602 | hp1 | a0001 | c0001 | t0010 | g0040 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02602 | hp2 | a0001 | c0002 | t0004 | g0175 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0049 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0133 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0062 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03041 | hp1 | a0001 | c0001 | t0012 | g0104 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0061 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0056 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03139 | hp2 | a0001 | c0001 | t0012 | g0013 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0210 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0057 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0067 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03490 | hp1 | a0001 | c0002 | t0004 | g0003 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0050 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03579 | hp2 | a0001 | c0001 | t0011 | g0211 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0129 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0113 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03669 | hp1 | a0001 | c0002 | t0004 | g0176 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | STU | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0131 | SAS | BEB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0031 | SAS | BEB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03834 | hp1 | a0001 | c0001 | t0010 | g0040 | SAS | BEB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03927 | hp1 | a0001 | c0001 | t0006 | g0066 | SAS | BEB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | BEB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0114 | SAS | STU | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | STU | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | STU | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | STU | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0055 | AFR | YRI | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18522 | hp2 | a0001 | c0001 | t0017 | g0111 | AFR | YRI | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18747 | hp1 | a0003 | c0005 | t0002 | g0193 | EAS | CHB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | CHB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | YRI | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18982 | hp1 | a0001 | c0004 | t0002 | g0069 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19004 | hp2 | a0001 | c0001 | t0016 | g0002 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | LWK | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19030 | hp2 | a0001 | c0001 | t0014 | g0058 | AFR | LWK | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | LWK | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | YRI | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0097 | AFR | ASW | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ASW | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA20752 | hp1 | a0001 | c0002 | t0004 | g0168 | EUR | TSI | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA20805 | hp2 | a0001 | c0002 | t0004 | g0007 | EUR | TSI | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | GIH | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | GIH | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01123 | hp1 | a0001 | c0002 | t0004 | g0003 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG01123 | hp2 | a0002 | c0003 | t0006 | g0065 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0003 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | USA | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | USA | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | USA | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | USA | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA21309 | hp1 | a0001 | c0002 | t0004 | g0007 | AFR | LWK | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0004 | g0003 | REF | REF | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0108 | REF | REF | MSANTD3_chr9_100422143_100456734 | MSANTD3 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:100442254
|
C | G | 1 | a0003 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.316C>G | p.Leu106Val | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/3 | 600/1880 | 316/828 | 106/275 | chr9 | 100442254 | ||
| chr9:100450728
|
A | G | 1 | a0002 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.590A>G | p.His197Arg | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 3/3 | 874/1880 | 590/828 | 197/275 | chr9 | 100450728 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:100442295
|
C | G | 1 | a0001c0002 | 23 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(20): Show |
synonymous_variant | LOW | c.357C>G | p.Leu119Leu | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/3 | 641/1880 | 357/828 | 119/275 | chr9 | 100442295 | ||
| chr9:100442340
|
C | T | 1 | a0001c0004 | 1 | NA18982.hp1 | synonymous_variant | LOW | c.402C>T | p.Pro134Pro | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/3 | 686/1880 | 402/828 | 134/275 | chr9 | 100442340 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:100427257
|
C | T | 1 | a0001c0001t0005 | 12 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-170C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/3 | chr9 | 100427257 | ||||||
| chr9:100427278
|
T | C | 13 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(10): Show | 99 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(96): Show |
5_prime_UTR_variant | MODIFIER | c.-149T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/3 | 14661 | chr9 | 100427278 | |||||
| chr9:100427280
|
C | T | 1 | a0001c0001t0013 | 2 | HG01099.hp2 HG01192.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-147C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/3 | chr9 | 100427280 | ||||||
| chr9:100427313
|
G | A | 1 | a0001c0001t0009 | 2 | HG00733.hp1 HG03098.hp1 |
5_prime_UTR_variant | MODIFIER | c.-114G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/3 | 14626 | chr9 | 100427313 | |||||
| chr9:100427325
|
C | T | 4 | a0001c0001t0002a0001c0001t0016a0001c0004t0002others(1): Show | 56 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
5_prime_UTR_variant | MODIFIER | c.-102C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/3 | 14614 | chr9 | 100427325 | |||||
| chr9:100451232
|
C | T | 3 | a0001c0001t0004a0001c0002t0004a0001c0002t0015 | 26 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*266C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 3/3 | 266 | chr9 | 100451232 | |||||
| chr9:100451258
|
T | TG | 1 | a0001c0001t0007 | 7 | HG01891.hp1 HG02280.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*292_*293insG | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 3/3 | 293 | chr9 | 100451258 | |||||
| chr9:100451305
|
AT | A | 15 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(12): Show | 261 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(258): Show |
3_prime_UTR_variant | MODIFIER | c.*352delT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 3/3 | 352 | INFO_REALIGN_3_PRIME | chr9 | 100451305 | ||||
| chr9:100451374
|
A | G | 2 | a0001c0001t0007a0001c0001t0009 | 9 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*408A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 3/3 | 408 | chr9 | 100451374 | |||||
| chr9:100451413
|
A | G | 1 | a0001c0001t0011 | 2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*447A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 3/3 | 447 | chr9 | 100451413 | |||||
| chr9:100451461
|
C | T | 1 | a0001c0001t0018 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*495C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 3/3 | 495 | chr9 | 100451461 | |||||
| chr9:100451663
|
G | A | 1 | a0001c0001t0009 | 2 | HG00733.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*697G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 3/3 | 697 | chr9 | 100451663 | |||||
| chr9:100451665
|
A | G | 20 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(17): Show | 273 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*699A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 3/3 | 699 | chr9 | 100451665 | |||||
| chr9:100451711
|
TA | T | 8 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(5): Show | 52 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*759delA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 3/3 | 759 | INFO_REALIGN_3_PRIME | chr9 | 100451711 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:100427426
|
C | CGGGCGG | 7 | a0001c0001t0001g0022a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 8 | HG01069.hp2 HG01074.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34+43_-34+48dupCG others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100427426 | |||||
| chr9:100427461
|
G | C | 8 | a0001c0001t0005g0012a0001c0001t0005g0023a0001c0001t0005g0024others(5): Show | 12 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-34+68G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100427461 | ||||||
| chr9:100427468
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-34+75G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100427468 | ||||||
| chr9:100427769
|
C | T | 2 | a0001c0001t0011g0210a0001c0001t0011g0211 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-34+376C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100427769 | ||||||
| chr9:100427896
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-34+503C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100427896 | ||||||
| chr9:100428051
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-34+658G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100428051 | ||||||
| chr9:100428112
|
C | A | 1 | a0001c0001t0001g0054 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-34+719C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100428112 | ||||||
| chr9:100428174
|
A | G | 37 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0002g0002others(34): Show | 58 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.-34+781A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100428174 | ||||||
| chr9:100428392
|
CAT | C | 3 | a0001c0001t0008g0055a0001c0001t0008g0056a0001c0001t0008g0057 | 3 | HG03098.hp2 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-34+1001_-34+1002d others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100428392 | |||||
| chr9:100428433
|
A | G | 20 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(17): Show | 31 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-34+1040A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100428433 | ||||||
| chr9:100428490
|
G | A | 2 | a0001c0001t0011g0210a0001c0001t0011g0211 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-34+1097G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100428490 | ||||||
| chr9:100428666
|
G | C | 2 | a0001c0001t0011g0210a0001c0001t0011g0211 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-34+1273G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100428666 | ||||||
| chr9:100428785
|
A | G | 1 | a0001c0001t0010g0040 | 2 | HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-34+1392A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100428785 | ||||||
| chr9:100428966
|
A | T | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-34+1573A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100428966 | ||||||
| chr9:100429011
|
C | T | 1 | a0001c0001t0011g0211 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-34+1618C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100429011 | ||||||
| chr9:100429045
|
G | A | 1 | a0001c0001t0014g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-34+1652G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100429045 | ||||||
| chr9:100429084
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-34+1691G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100429084 | ||||||
| chr9:100429179
|
A | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0165a0001c0001t0001g0166 | 6 | HG01081.hp2 HG01243.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+1786A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100429179 | ||||||
| chr9:100429194
|
G | C | 1 | a0001c0001t0001g0059 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-34+1801G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100429194 | ||||||
| chr9:100429707
|
G | GT | 8 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(5): Show | 8 | HG00438.hp2 HG01099.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34+2324dupT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100429707 | |||||
| chr9:100429707
|
GT | G | 19 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(16): Show | 30 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-34+2324delT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100429707 | |||||
| chr9:100429720
|
G | C | 4 | a0001c0001t0007g0006a0001c0001t0007g0062a0001c0001t0009g0060others(1): Show | 9 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-34+2327G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100429720 | ||||||
| chr9:100429777
|
A | T | 1 | a0001c0001t0001g0159 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-34+2384A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100429777 | ||||||
| chr9:100429782
|
A | C | 3 | a0001c0001t0003g0018a0001c0001t0003g0157a0001c0001t0003g0158 | 5 | NA18954.hp1 NA18989.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34+2389A>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100429782 | ||||||
| chr9:100429992
|
C | T | 1 | a0001c0001t0014g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-34+2599C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100429992 | ||||||
| chr9:100430081
|
TCTC | T | 4 | a0001c0001t0007g0006a0001c0001t0007g0062a0001c0001t0009g0060others(1): Show | 9 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-34+2692_-34+2694d others(5): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100430081 | |||||
| chr9:100430095
|
C | CA | 30 | a0001c0001t0001g0025a0001c0001t0001g0064a0001c0001t0001g0183others(27): Show | 42 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.-34+2721dupA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100430095 | |||||
| chr9:100430095
|
CA | C | 6 | a0001c0001t0001g0037a0001c0001t0001g0156a0001c0001t0002g0206others(3): Show | 7 | HG02165.hp1 HG02165.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-34+2721delA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100430095 | |||||
| chr9:100430260
|
A | C | 1 | a0001c0001t0010g0040 | 2 | HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-34+2867A>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100430260 | ||||||
| chr9:100430270
|
G | A | 20 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(17): Show | 31 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-34+2877G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100430270 | ||||||
| chr9:100430324
|
C | CA | 48 | a0001c0001t0001g0011a0001c0001t0001g0071a0001c0001t0001g0165others(45): Show | 76 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-34+2949dupA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100430324 | |||||
| chr9:100430324
|
C | CAA | 6 | a0001c0001t0002g0184a0001c0001t0002g0206a0001c0001t0007g0006others(3): Show | 11 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-34+2948_-34+2949d others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100430324 | |||||
| chr9:100430324
|
CA | C | 21 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(18): Show | 32 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.-34+2949delA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100430324 | |||||
| chr9:100430341
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-34+2948A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100430341 | ||||||
| chr9:100430403
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-34+3010G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100430403 | ||||||
| chr9:100430469
|
A | G | 3 | a0001c0001t0001g0036a0001c0001t0001g0149a0001c0001t0001g0150 | 4 | HG01884.hp2 HG02258.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34+3076A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100430469 | ||||||
| chr9:100430825
|
T | C | 4 | a0001c0001t0003g0026a0001c0001t0003g0073a0001c0001t0003g0074others(1): Show | 5 | HG02145.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34+3432T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100430825 | ||||||
| chr9:100430858
|
A | G | 1 | a0001c0001t0002g0203 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-34+3465A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100430858 | ||||||
| chr9:100430861
|
G | A | 20 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(17): Show | 31 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-34+3468G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100430861 | ||||||
| chr9:100430963
|
G | A | 1 | a0001c0001t0003g0076 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-34+3570G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100430963 | ||||||
| chr9:100431024
|
T | C | 64 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0002g0002others(61): Show | 101 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.-34+3631T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100431024 | ||||||
| chr9:100431071
|
C | T | 20 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(17): Show | 31 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-34+3678C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100431071 | ||||||
| chr9:100431079
|
C | T | 39 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0002g0002others(36): Show | 60 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.-34+3686C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100431079 | ||||||
| chr9:100431301
|
C | CT | 9 | a0001c0001t0001g0052a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG00741.hp1 HG01884.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.-34+3927dupT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100431301 | |||||
| chr9:100431301
|
CT | C | 39 | a0001c0001t0001g0011a0001c0001t0001g0077a0001c0001t0001g0078others(36): Show | 58 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.-34+3927delT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100431301 | |||||
| chr9:100431301
|
CTT | C | 6 | a0001c0001t0001g0165a0001c0001t0007g0006a0001c0001t0007g0062others(3): Show | 11 | HG00733.hp1 HG01081.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.-34+3926_-34+3927d others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100431301 | |||||
| chr9:100431425
|
C | T | 1 | a0001c0001t0003g0068 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-34+4032C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100431425 | ||||||
| chr9:100431546
|
T | TC | 75 | a0001c0001t0001g0011a0001c0001t0001g0165a0001c0001t0001g0166others(72): Show | 119 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.-34+4158dupC | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100431546 | |||||
| chr9:100431614
|
C | CT | 20 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(17): Show | 31 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-34+4230dupT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100431614 | |||||
| chr9:100431667
|
T | A | 20 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(17): Show | 31 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-34+4274T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100431667 | ||||||
| chr9:100431825
|
G | A | 20 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(17): Show | 31 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-34+4432G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100431825 | ||||||
| chr9:100431832
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-34+4439G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100431832 | ||||||
| chr9:100432187
|
G | C | 6 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(3): Show | 6 | HG02145.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34+4794G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100432187 | ||||||
| chr9:100432228
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-34+4835G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100432228 | ||||||
| chr9:100432245
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-34+4852G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100432245 | ||||||
| chr9:100432248
|
A | C | 1 | a0001c0001t0005g0050 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-34+4855A>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100432248 | ||||||
| chr9:100432357
|
A | G | 3 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0003g0148 | 3 | HG00741.hp2 HG01099.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.-34+4964A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100432357 | ||||||
| chr9:100432457
|
G | A | 20 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(17): Show | 31 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-34+5064G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100432457 | ||||||
| chr9:100432474
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0155 | 2 | HG01952.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-34+5081G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100432474 | ||||||
| chr9:100432787
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-34+5394T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100432787 | ||||||
| chr9:100433086
|
A | C | 2 | a0001c0001t0011g0210a0001c0001t0011g0211 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-34+5693A>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433086 | ||||||
| chr9:100433135
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-34+5742G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433135 | ||||||
| chr9:100433272
|
A | G | 1 | a0001c0001t0014g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-34+5879A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433272 | ||||||
| chr9:100433431
|
A | G | 5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0080others(2): Show | 6 | HG01099.hp2 HG01192.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+6038A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433431 | ||||||
| chr9:100433451
|
C | T | 2 | a0001c0001t0011g0210a0001c0001t0011g0211 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-34+6058C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433451 | ||||||
| chr9:100433505
|
G | A | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-34+6112G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433505 | ||||||
| chr9:100433510
|
T | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0165a0001c0001t0001g0166 | 6 | HG01081.hp2 HG01243.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+6117T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433510 | ||||||
| chr9:100433644
|
T | G | 64 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0002g0002others(61): Show | 101 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.-34+6251T>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433644 | ||||||
| chr9:100433820
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-34+6427C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433820 | ||||||
| chr9:100433859
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-34+6466G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433859 | ||||||
| chr9:100433872
|
G | A | 2 | a0001c0001t0011g0210a0001c0001t0011g0211 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-34+6479G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433872 | ||||||
| chr9:100433929
|
G | A | 75 | a0001c0001t0001g0011a0001c0001t0001g0165a0001c0001t0001g0166others(72): Show | 119 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.-34+6536G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433929 | ||||||
| chr9:100433977
|
G | A | 15 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(12): Show | 26 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.-34+6584G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433977 | ||||||
| chr9:100434016
|
C | A | 1 | a0001c0001t0001g0161 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-34+6623C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434016 | ||||||
| chr9:100434106
|
A | G | 1 | a0001c0001t0014g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-34+6713A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434106 | ||||||
| chr9:100434124
|
A | G | 2 | a0001c0001t0011g0210a0001c0001t0011g0211 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-34+6731A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434124 | ||||||
| chr9:100434192
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-34+6799A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434192 | ||||||
| chr9:100434286
|
G | A | 1 | a0001c0001t0014g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-34+6893G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434286 | ||||||
| chr9:100434458
|
A | C | 1 | a0001c0001t0003g0164 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-34+7065A>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434458 | ||||||
| chr9:100434508
|
C | T | 1 | a0001c0001t0014g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-34+7115C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434508 | ||||||
| chr9:100434542
|
G | GA | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-34+7152dupA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100434542 | |||||
| chr9:100434621
|
T | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0165a0001c0001t0001g0166 | 6 | HG01081.hp2 HG01243.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+7228T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434621 | ||||||
| chr9:100434970
|
T | TAC | 12 | a0001c0001t0001g0022a0001c0001t0001g0042a0001c0001t0001g0043others(9): Show | 16 | HG01069.hp2 HG01074.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.-33-6917_-33-6916d others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100434970 | |||||
| chr9:100434970
|
T | TACAC | 2 | a0001c0001t0005g0023a0001c0001t0005g0047 | 3 | HG01891.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-33-6919_-33-6916d others(6): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100434970 | |||||
| chr9:100434970
|
TAC | T | 19 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(16): Show | 30 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-33-6917_-33-6916d others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100434970 | |||||
| chr9:100434987
|
A | G | 3 | a0001c0001t0002g0039a0001c0001t0002g0208a0001c0001t0010g0040 | 5 | HG02602.hp1 HG03834.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33-6919A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434987 | ||||||
| chr9:100434989
|
A | G | 61 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0002g0002others(58): Show | 98 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.-33-6917A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434989 | ||||||
| chr9:100434992
|
T | C | 62 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0002g0002others(59): Show | 99 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.-33-6914T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434992 | ||||||
| chr9:100435007
|
T | A | 2 | a0001c0001t0011g0210a0001c0001t0011g0211 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-33-6899T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435007 | ||||||
| chr9:100435116
|
G | A | 2 | a0001c0001t0003g0091a0001c0001t0003g0092 | 2 | NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-33-6790G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435116 | ||||||
| chr9:100435242
|
C | T | 8 | a0001c0001t0005g0012a0001c0001t0005g0023a0001c0001t0005g0024others(5): Show | 12 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-33-6664C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435242 | ||||||
| chr9:100435295
|
A | G | 38 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0002g0002others(35): Show | 58 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.-33-6611A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435295 | ||||||
| chr9:100435358
|
C | G | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-33-6548C>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435358 | ||||||
| chr9:100435503
|
T | G | 1 | a0001c0001t0001g0093 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-33-6403T>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435503 | ||||||
| chr9:100435597
|
G | A | 1 | a0001c0001t0003g0094 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-33-6309G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435597 | ||||||
| chr9:100435601
|
T | A | 1 | a0001c0001t0001g0095 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-33-6305T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435601 | ||||||
| chr9:100435665
|
G | A | 2 | a0001c0001t0011g0210a0001c0001t0011g0211 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-33-6241G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435665 | ||||||
| chr9:100435685
|
T | C | 8 | a0001c0001t0005g0012a0001c0001t0005g0023a0001c0001t0005g0024others(5): Show | 12 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-33-6221T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435685 | ||||||
| chr9:100435709
|
A | G | 2 | a0001c0001t0011g0210a0001c0001t0011g0211 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-33-6197A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435709 | ||||||
| chr9:100435968
|
A | C | 1 | a0001c0001t0002g0201 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-33-5938A>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435968 | ||||||
| chr9:100436166
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-33-5740C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436166 | ||||||
| chr9:100436453
|
C | T | 2 | a0001c0001t0011g0210a0001c0001t0011g0211 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-33-5453C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436453 | ||||||
| chr9:100436464
|
C | T | 1 | a0001c0001t0003g0067 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-33-5442C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436464 | ||||||
| chr9:100436471
|
A | G | 8 | a0001c0001t0005g0012a0001c0001t0005g0023a0001c0001t0005g0024others(5): Show | 12 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-33-5435A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436471 | ||||||
| chr9:100436645
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-33-5261G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436645 | ||||||
| chr9:100436738
|
G | A | 4 | a0001c0001t0007g0006a0001c0001t0007g0062a0001c0001t0009g0060others(1): Show | 9 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-33-5168G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436738 | ||||||
| chr9:100436805
|
C | G | 1 | a0001c0001t0001g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-33-5101C>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436805 | ||||||
| chr9:100436835
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-33-5071C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436835 | ||||||
| chr9:100436868
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-33-5038G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436868 | ||||||
| chr9:100436891
|
G | A | 1 | a0001c0001t0009g0060 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-33-5015G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436891 | ||||||
| chr9:100436964
|
C | G | 1 | a0001c0001t0003g0041 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-33-4942C>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436964 | ||||||
| chr9:100437002
|
G | A | 19 | a0001c0001t0002g0188a0001c0001t0004g0169a0001c0001t0004g0170others(16): Show | 30 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-33-4904G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100437002 | ||||||
| chr9:100437016
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0165a0001c0001t0001g0166 | 6 | HG01081.hp2 HG01243.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33-4890G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100437016 | ||||||
| chr9:100437321
|
A | G | 1 | a0001c0001t0002g0187 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-33-4585A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100437321 | ||||||
| chr9:100437404
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0001g0077a0001c0001t0001g0136others(2): Show | 8 | NA18940.hp1 NA18946.hp1 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-33-4502C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100437404 | ||||||
| chr9:100437683
|
T | G | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-33-4223T>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100437683 | ||||||
| chr9:100437712
|
A | G | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-33-4194A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100437712 | ||||||
| chr9:100437976
|
T | G | 1 | a0001c0001t0002g0207 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-33-3930T>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100437976 | ||||||
| chr9:100438305
|
C | T | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-33-3601C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100438305 | ||||||
| chr9:100438317
|
A | G | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-33-3589A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100438317 | ||||||
| chr9:100438333
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-33-3573A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100438333 | ||||||
| chr9:100438427
|
A | AGT | 12 | a0001c0001t0001g0059a0001c0001t0001g0132a0001c0001t0001g0138others(9): Show | 13 | HG00642.hp1 HG00738.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.-33-3462_-33-3461d others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100438427 | |||||
| chr9:100438427
|
A | AGTGTGTG others(1): Show |
18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-33-3468_-33-3461d others(10): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100438427 | |||||
| chr9:100438430
|
G | A | 39 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0002g0002others(36): Show | 60 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.-33-3476G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100438430 | ||||||
| chr9:100438431
|
T | A | 39 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0002g0002others(36): Show | 60 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.-33-3475T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100438431 | ||||||
| chr9:100438611
|
G | A | 2 | a0001c0001t0009g0060a0001c0001t0009g0061 | 2 | HG00733.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-33-3295G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100438611 | ||||||
| chr9:100438638
|
G | A | 1 | a0001c0001t0010g0040 | 2 | HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-33-3268G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100438638 | ||||||
| chr9:100438759
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-33-3147G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100438759 | ||||||
| chr9:100439128
|
A | T | 2 | a0001c0002t0004g0175a0001c0002t0004g0176 | 2 | HG02602.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-33-2778A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100439128 | ||||||
| chr9:100439179
|
A | G | 1 | a0001c0001t0003g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-33-2727A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100439179 | ||||||
| chr9:100439372
|
T | C | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-33-2534T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100439372 | ||||||
| chr9:100439515
|
T | A | 68 | a0001c0001t0001g0183a0001c0001t0002g0002a0001c0001t0002g0019others(65): Show | 109 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.-33-2391T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100439515 | ||||||
| chr9:100439518
|
T | A | 1 | a0001c0001t0002g0206 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-33-2388T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100439518 | ||||||
| chr9:100439604
|
G | A | 1 | a0001c0001t0004g0169 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-33-2302G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100439604 | ||||||
| chr9:100439605
|
G | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0093a0001c0001t0001g0126others(2): Show | 8 | HG02258.hp2 HG02615.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-33-2301G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100439605 | ||||||
| chr9:100439676
|
A | AT | 9 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0162others(6): Show | 11 | HG00544.hp1 HG01070.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.-33-2214dupT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100439676 | |||||
| chr9:100439785
|
C | T | 2 | a0001c0001t0003g0091a0001c0001t0003g0092 | 2 | NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-33-2121C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100439785 | ||||||
| chr9:100439953
|
A | C | 1 | a0001c0001t0001g0124 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-33-1953A>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100439953 | ||||||
| chr9:100439969
|
A | G | 3 | a0001c0001t0002g0038a0001c0001t0002g0198a0001c0001t0002g0205 | 4 | HG00408.hp2 NA18747.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33-1937A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100439969 | ||||||
| chr9:100440017
|
G | A | 1 | a0001c0001t0003g0096 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-33-1889G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440017 | ||||||
| chr9:100440073
|
G | C | 2 | a0001c0001t0003g0063a0001c0001t0003g0097 | 2 | HG02572.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-33-1833G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440073 | ||||||
| chr9:100440210
|
G | A | 3 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0130 | 3 | HG01255.hp2 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-33-1696G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440210 | ||||||
| chr9:100440232
|
G | C | 1 | a0001c0001t0014g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-33-1674G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440232 | ||||||
| chr9:100440241
|
C | T | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-33-1665C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440241 | ||||||
| chr9:100440308
|
T | C | 75 | a0001c0001t0001g0011a0001c0001t0001g0165a0001c0001t0001g0166others(72): Show | 119 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.-33-1598T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440308 | ||||||
| chr9:100440330
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-33-1576T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440330 | ||||||
| chr9:100440510
|
T | G | 5 | a0001c0001t0001g0064a0001c0001t0001g0078a0001c0001t0001g0100others(2): Show | 5 | HG02129.hp2 NA18954.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33-1396T>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440510 | ||||||
| chr9:100440585
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-33-1321G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440585 | ||||||
| chr9:100440587
|
C | CA | 4 | a0001c0001t0007g0006a0001c0001t0007g0062a0001c0001t0009g0060others(1): Show | 9 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-33-1316dupA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100440587 | |||||
| chr9:100440590
|
A | AT | 9 | a0001c0001t0001g0016a0001c0001t0001g0045a0001c0001t0001g0086others(6): Show | 11 | HG01074.hp2 HG01255.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-33-1297dupT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100440590 | |||||
| chr9:100440590
|
AT | A | 63 | a0001c0001t0001g0082a0001c0001t0001g0103a0001c0001t0001g0183others(60): Show | 95 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.-33-1297delT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100440590 | |||||
| chr9:100440591
|
T | A | 8 | a0001c0001t0005g0012a0001c0001t0005g0023a0001c0001t0005g0024others(5): Show | 12 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-33-1315T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440591 | ||||||
| chr9:100440592
|
T | A | 8 | a0001c0001t0005g0012a0001c0001t0005g0023a0001c0001t0005g0024others(5): Show | 12 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-33-1314T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440592 | ||||||
| chr9:100440722
|
C | G | 39 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0002g0002others(36): Show | 60 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.-33-1184C>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440722 | ||||||
| chr9:100440780
|
C | CT | 60 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0033others(57): Show | 87 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.-33-1099dupT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100440780 | |||||
| chr9:100440780
|
C | CTT | 16 | a0001c0001t0001g0044a0001c0001t0001g0183a0001c0001t0001g0186others(13): Show | 18 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.-33-1100_-33-1099d others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100440780 | |||||
| chr9:100440780
|
C | CTTT | 5 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0120others(2): Show | 7 | HG00558.hp2 HG00621.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-1101_-33-1099d others(5): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100440780 | |||||
| chr9:100440780
|
C | T | 1 | a0001c0001t0002g0206 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-33-1126C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440780 | ||||||
| chr9:100440780
|
CT | C | 9 | a0001c0001t0001g0083a0001c0001t0001g0105a0001c0001t0001g0106others(6): Show | 13 | HG00733.hp1 HG01256.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-33-1099delT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100440780 | |||||
| chr9:100440780
|
CTTTTTT | C | 16 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(13): Show | 27 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.-33-1104_-33-1099d others(8): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100440780 | |||||
| chr9:100440806
|
T | A | 1 | a0001c0001t0001g0161 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-33-1100T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440806 | ||||||
| chr9:100440921
|
G | A | 1 | a0001c0001t0011g0210 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-33-985G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440921 | ||||||
| chr9:100440931
|
C | CT | 28 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0093others(25): Show | 34 | HG00438.hp2 HG00733.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.-33-953dupT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100440931 | |||||
| chr9:100440931
|
CT | C | 21 | a0001c0001t0001g0022a0001c0001t0001g0027a0001c0001t0001g0072others(18): Show | 33 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.-33-953delT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100440931 | |||||
| chr9:100441000
|
A | G | 1 | a0001c0001t0014g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-33-906A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100441000 | ||||||
| chr9:100441355
|
C | T | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-33-551C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100441355 | ||||||
| chr9:100441444
|
C | G | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-33-462C>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100441444 | ||||||
| chr9:100441544
|
C | T | 8 | a0001c0001t0005g0012a0001c0001t0005g0023a0001c0001t0005g0024others(5): Show | 12 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-33-362C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100441544 | ||||||
| chr9:100441635
|
G | A | 3 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0047 | 5 | HG01891.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33-271G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100441635 | ||||||
| chr9:100441639
|
C | CA | 8 | a0001c0001t0005g0012a0001c0001t0005g0023a0001c0001t0005g0024others(5): Show | 12 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-33-257dupA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100441639 | |||||
| chr9:100442362
|
C | T | 1 | a0001c0001t0002g0188 | 1 | HG03688.hp2 | splice_region_variant&intron_variant | LOW | c.418+6C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100442362 | ||||||
| chr9:100442513
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.418+157A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100442513 | ||||||
| chr9:100442543
|
G | A | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.418+187G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100442543 | ||||||
| chr9:100442808
|
C | CA | 18 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0071others(15): Show | 20 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.418+473dupA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100442808 | |||||
| chr9:100442808
|
CA | C | 6 | a0001c0001t0001g0077a0001c0001t0002g0180a0001c0001t0002g0206others(3): Show | 11 | HG01891.hp1 HG02056.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.418+473delA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100442808 | |||||
| chr9:100442808
|
CAA | C | 37 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0002g0002others(34): Show | 58 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.418+472_418+473del others(2): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100442808 | |||||
| chr9:100442979
|
A | C | 1 | a0001c0001t0002g0197 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.418+623A>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100442979 | ||||||
| chr9:100443042
|
A | C | 3 | a0001c0001t0008g0055a0001c0001t0008g0056a0001c0001t0008g0057 | 3 | HG03098.hp2 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.418+686A>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443042 | ||||||
| chr9:100443117
|
C | T | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.418+761C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443117 | ||||||
| chr9:100443215
|
C | T | 1 | a0001c0001t0012g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.418+859C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443215 | ||||||
| chr9:100443329
|
G | T | 2 | a0001c0001t0011g0210a0001c0001t0011g0211 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.418+973G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443329 | ||||||
| chr9:100443372
|
G | C | 72 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0002g0002others(69): Show | 113 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.418+1016G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443372 | ||||||
| chr9:100443395
|
A | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(215): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.418+1039A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443395 | ||||||
| chr9:100443399
|
CA | C | 20 | a0001c0001t0001g0209a0001c0001t0002g0196a0001c0001t0004g0169others(17): Show | 32 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.418+1057delA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100443399 | |||||
| chr9:100443403
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.418+1047A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443403 | ||||||
| chr9:100443471
|
G | A | 4 | a0001c0001t0007g0006a0001c0001t0007g0062a0001c0001t0009g0060others(1): Show | 9 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.418+1115G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443471 | ||||||
| chr9:100443581
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.418+1225T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443581 | ||||||
| chr9:100443621
|
A | G | 1 | a0001c0001t0006g0133 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.418+1265A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443621 | ||||||
| chr9:100443677
|
G | C | 1 | a0001c0001t0001g0109 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.418+1321G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443677 | ||||||
| chr9:100443742
|
G | A | 38 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0002g0002others(35): Show | 58 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.418+1386G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443742 | ||||||
| chr9:100443778
|
T | G | 1 | a0001c0001t0001g0033 | 2 | HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.418+1422T>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443778 | ||||||
| chr9:100443807
|
A | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0107 | 2 | NA19002.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.418+1451A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443807 | ||||||
| chr9:100443901
|
C | T | 1 | a0001c0001t0014g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.418+1545C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443901 | ||||||
| chr9:100444048
|
G | A | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.418+1692G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100444048 | ||||||
| chr9:100444133
|
C | T | 8 | a0001c0001t0003g0004a0001c0001t0003g0018a0001c0001t0003g0031others(5): Show | 17 | HG00140.hp2 HG00735.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.418+1777C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100444133 | ||||||
| chr9:100444137
|
C | A | 10 | a0001c0001t0001g0015a0001c0001t0001g0034a0001c0001t0001g0035others(7): Show | 13 | HG00558.hp2 HG00621.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.418+1781C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100444137 | ||||||
| chr9:100444370
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.418+2014G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100444370 | ||||||
| chr9:100444708
|
G | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0042a0001c0001t0001g0046others(2): Show | 7 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.418+2352G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100444708 | ||||||
| chr9:100444748
|
T | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0165a0001c0001t0001g0166 | 6 | HG01081.hp2 HG01243.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+2392T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100444748 | ||||||
| chr9:100444760
|
C | G | 1 | a0001c0001t0001g0115 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.418+2404C>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100444760 | ||||||
| chr9:100444912
|
C | T | 1 | a0001c0001t0010g0040 | 2 | HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.418+2556C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100444912 | ||||||
| chr9:100445001
|
C | T | 2 | a0001c0001t0001g0139a0001c0001t0001g0159 | 2 | HG04228.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.418+2645C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100445001 | ||||||
| chr9:100445098
|
AGGTAGGG others(4): Show |
A | 1 | a0001c0001t0003g0092 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.418+2747_418+2757d others(13): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100445098 | |||||
| chr9:100445213
|
C | T | 1 | a0001c0001t0003g0076 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.418+2857C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100445213 | ||||||
| chr9:100445372
|
G | A | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.418+3016G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100445372 | ||||||
| chr9:100445427
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.418+3071A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100445427 | ||||||
| chr9:100445709
|
T | A | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.418+3353T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100445709 | ||||||
| chr9:100445727
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.418+3371A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100445727 | ||||||
| chr9:100445788
|
G | T | 1 | a0001c0001t0001g0054 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.418+3432G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100445788 | ||||||
| chr9:100445849
|
C | G | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.418+3493C>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100445849 | ||||||
| chr9:100445860
|
G | A | 4 | a0001c0001t0007g0006a0001c0001t0007g0062a0001c0001t0009g0060others(1): Show | 9 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.418+3504G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100445860 | ||||||
| chr9:100446007
|
C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3651C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446007 | ||||||
| chr9:100446010
|
C | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3654C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446010 | ||||||
| chr9:100446011
|
C | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3655C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446011 | ||||||
| chr9:100446015
|
A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3659A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446015 | ||||||
| chr9:100446016
|
T | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3660T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446016 | ||||||
| chr9:100446017
|
T | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3661T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446017 | ||||||
| chr9:100446020
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3664G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446020 | ||||||
| chr9:100446022
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3666G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446022 | ||||||
| chr9:100446023
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3667G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446023 | ||||||
| chr9:100446024
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3668G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446024 | ||||||
| chr9:100446025
|
C | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3669C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446025 | ||||||
| chr9:100446027
|
A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3671A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446027 | ||||||
| chr9:100446028
|
C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3672C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446028 | ||||||
| chr9:100446030
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3674G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446030 | ||||||
| chr9:100446032
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3676G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446032 | ||||||
| chr9:100446035
|
C | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3679C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446035 | ||||||
| chr9:100446036
|
A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3680A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446036 | ||||||
| chr9:100446037
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3681G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446037 | ||||||
| chr9:100446038
|
A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3682A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446038 | ||||||
| chr9:100446039
|
A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3683A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446039 | ||||||
| chr9:100446040
|
C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3684C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446040 | ||||||
| chr9:100446041
|
C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3685C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446041 | ||||||
| chr9:100446044
|
C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3688C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446044 | ||||||
| chr9:100446050
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3694G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446050 | ||||||
| chr9:100446052
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3696G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446052 | ||||||
| chr9:100446053
|
C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3697C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446053 | ||||||
| chr9:100446054
|
C | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3698C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446054 | ||||||
| chr9:100446056
|
A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3700A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446056 | ||||||
| chr9:100446060
|
A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3704A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446060 | ||||||
| chr9:100446061
|
A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3705A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446061 | ||||||
| chr9:100446064
|
C | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3708C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446064 | ||||||
| chr9:100446065
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3709G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446065 | ||||||
| chr9:100446066
|
C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3710C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446066 | ||||||
| chr9:100446069
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3713G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446069 | ||||||
| chr9:100446070
|
G | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3714G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446070 | ||||||
| chr9:100446071
|
A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3715A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446071 | ||||||
| chr9:100446072
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3716G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446072 | ||||||
| chr9:100446074
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3718G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446074 | ||||||
| chr9:100446075
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3719G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446075 | ||||||
| chr9:100446076
|
C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3720C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446076 | ||||||
| chr9:100446078
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3722G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446078 | ||||||
| chr9:100446079
|
G | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3723G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446079 | ||||||
| chr9:100446080
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3724G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446080 | ||||||
| chr9:100446082
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3726G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446082 | ||||||
| chr9:100446083
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3727G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446083 | ||||||
| chr9:100446084
|
C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3728C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446084 | ||||||
| chr9:100446087
|
G | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3731G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446087 | ||||||
| chr9:100446088
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3732G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446088 | ||||||
| chr9:100446089
|
A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3733A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446089 | ||||||
| chr9:100446091
|
G | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3735G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446091 | ||||||
| chr9:100446093
|
C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3737C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446093 | ||||||
| chr9:100446094
|
C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3738C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446094 | ||||||
| chr9:100446099
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3743G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446099 | ||||||
| chr9:100446101
|
C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3745C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446101 | ||||||
| chr9:100446102
|
A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3746A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446102 | ||||||
| chr9:100446114
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3758G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446114 | ||||||
| chr9:100446117
|
A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3761A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446117 | ||||||
| chr9:100446118
|
A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3762A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446118 | ||||||
| chr9:100446119
|
C | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3763C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446119 | ||||||
| chr9:100446121
|
A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3765A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446121 | ||||||
| chr9:100446122
|
A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3766A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446122 | ||||||
| chr9:100446123
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3767G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446123 | ||||||
| chr9:100446124
|
C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3768C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446124 | ||||||
| chr9:100446129
|
G | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3773G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446129 | ||||||
| chr9:100446131
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3775G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446131 | ||||||
| chr9:100446133
|
A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3777A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446133 | ||||||
| chr9:100446134
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3778G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446134 | ||||||
| chr9:100446135
|
C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3779C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446135 | ||||||
| chr9:100446137
|
C | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3781C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446137 | ||||||
| chr9:100446138
|
C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3782C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446138 | ||||||
| chr9:100446141
|
G | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3785G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446141 | ||||||
| chr9:100446142
|
A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3786A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446142 | ||||||
| chr9:100446144
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3788G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446144 | ||||||
| chr9:100446146
|
C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3790C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446146 | ||||||
| chr9:100446148
|
T | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3792T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446148 | ||||||
| chr9:100446150
|
G | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3794G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446150 | ||||||
| chr9:100446151
|
G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3795G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446151 | ||||||
| chr9:100446152
|
A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3796A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446152 | ||||||
| chr9:100446178
|
A | G | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.418+3822A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446178 | ||||||
| chr9:100446224
|
G | A | 39 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0002g0002others(36): Show | 60 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.418+3868G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446224 | ||||||
| chr9:100446364
|
A | G | 1 | a0001c0001t0001g0154 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.418+4008A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446364 | ||||||
| chr9:100446414
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0001g0077a0001c0001t0001g0136others(2): Show | 8 | NA18940.hp1 NA18946.hp1 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.418+4058C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446414 | ||||||
| chr9:100446417
|
G | A | 18 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0081others(15): Show | 19 | HG01255.hp2 HG01884.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.418+4061G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446417 | ||||||
| chr9:100446653
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.419-3904C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446653 | ||||||
| chr9:100446825
|
T | TA | 65 | a0001c0001t0001g0138a0001c0001t0001g0183a0001c0001t0001g0186others(62): Show | 102 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.419-3717dupA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100446825 | |||||
| chr9:100446825
|
T | TAA | 11 | a0001c0001t0001g0011a0001c0001t0001g0165a0001c0001t0001g0166others(8): Show | 18 | HG01081.hp2 HG01243.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.419-3718_419-3717d others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100446825 | |||||
| chr9:100447040
|
C | G | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.419-3517C>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100447040 | ||||||
| chr9:100447319
|
C | T | 1 | a0003c0005t0002g0193 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.419-3238C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100447319 | ||||||
| chr9:100447368
|
CT | C | 76 | a0001c0001t0001g0011a0001c0001t0001g0165a0001c0001t0001g0166others(73): Show | 120 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.419-3180delT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100447368 | |||||
| chr9:100447453
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.419-3104G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100447453 | ||||||
| chr9:100448059
|
G | C | 1 | a0001c0001t0001g0117 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.419-2498G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100448059 | ||||||
| chr9:100448092
|
G | A | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.419-2465G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100448092 | ||||||
| chr9:100448098
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.419-2459G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100448098 | ||||||
| chr9:100448143
|
A | T | 3 | a0001c0001t0002g0038a0001c0001t0002g0198a0001c0001t0002g0205 | 4 | HG00408.hp2 NA18747.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.419-2414A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100448143 | ||||||
| chr9:100448190
|
C | CA | 47 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0081others(44): Show | 64 | HG00408.hp2 HG00621.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.419-2343dupA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100448190 | |||||
| chr9:100448190
|
C | CAA | 11 | a0001c0001t0002g0021a0001c0001t0002g0039a0001c0001t0002g0194others(8): Show | 20 | HG00733.hp1 HG01070.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.419-2344_419-2343d others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100448190 | |||||
| chr9:100448190
|
CA | C | 18 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0035others(15): Show | 27 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-2343delA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100448190 | |||||
| chr9:100448190
|
CAA | C | 18 | a0001c0001t0004g0169a0001c0001t0004g0172a0001c0001t0005g0012others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.419-2344_419-2343d others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100448190 | |||||
| chr9:100448212
|
A | AG | 5 | a0001c0001t0002g0019a0001c0001t0002g0182a0001c0001t0002g0192others(2): Show | 7 | HG00423.hp1 HG00544.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.419-2345_419-2344i others(3): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100448212 | ||||||
| chr9:100448283
|
G | A | 1 | a0001c0002t0004g0175 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.419-2274G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100448283 | ||||||
| chr9:100448310
|
A | G | 4 | a0001c0001t0007g0006a0001c0001t0007g0062a0001c0001t0009g0060others(1): Show | 9 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.419-2247A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100448310 | ||||||
| chr9:100448491
|
G | C | 2 | a0001c0001t0011g0210a0001c0001t0011g0211 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.419-2066G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100448491 | ||||||
| chr9:100448536
|
G | A | 38 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0002g0002others(35): Show | 58 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.419-2021G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100448536 | ||||||
| chr9:100448805
|
C | T | 1 | a0001c0001t0006g0133 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.419-1752C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100448805 | ||||||
| chr9:100448951
|
CAGT | C | 4 | a0001c0001t0007g0006a0001c0001t0007g0062a0001c0001t0009g0060others(1): Show | 9 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.419-1603_419-1601d others(5): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100448951 | |||||
| chr9:100449043
|
C | T | 73 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0002g0002others(70): Show | 114 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.419-1514C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449043 | ||||||
| chr9:100449052
|
C | T | 9 | a0001c0001t0005g0012a0001c0001t0005g0023a0001c0001t0005g0024others(6): Show | 13 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.419-1505C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449052 | ||||||
| chr9:100449065
|
T | C | 1 | a0001c0001t0011g0211 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.419-1492T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449065 | ||||||
| chr9:100449111
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.419-1446G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449111 | ||||||
| chr9:100449114
|
C | T | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.419-1443C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449114 | ||||||
| chr9:100449163
|
C | G | 1 | a0001c0001t0003g0094 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.419-1394C>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449163 | ||||||
| chr9:100449163
|
C | T | 1 | a0001c0001t0003g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.419-1394C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449163 | ||||||
| chr9:100449235
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.419-1322C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449235 | ||||||
| chr9:100449325
|
C | T | 1 | a0001c0001t0004g0169 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.419-1232C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449325 | ||||||
| chr9:100449345
|
A | G | 1 | a0001c0001t0002g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.419-1212A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449345 | ||||||
| chr9:100449520
|
T | G | 76 | a0001c0001t0001g0011a0001c0001t0001g0165a0001c0001t0001g0166others(73): Show | 120 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.419-1037T>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449520 | ||||||
| chr9:100449695
|
G | A | 38 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0002g0002others(35): Show | 58 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.419-862G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449695 | ||||||
| chr9:100449741
|
G | T | 9 | a0001c0001t0005g0012a0001c0001t0005g0023a0001c0001t0005g0024others(6): Show | 13 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.419-816G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449741 | ||||||
| chr9:100449757
|
T | C | 18 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0172others(15): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.419-800T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449757 | ||||||
| chr9:100449827
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.419-730A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449827 | ||||||
| chr9:100449875
|
T | G | 1 | a0001c0001t0011g0210 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.419-682T>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449875 | ||||||
| chr9:100450081
|
G | C | 3 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075 | 3 | HG02145.hp1 HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.419-476G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100450081 | ||||||
| chr9:100450246
|
T | C | 39 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0002g0002others(36): Show | 60 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.419-311T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100450246 | ||||||
| chr9:100450446
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.419-111A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100450446 | ||||||
| chr9:100450462
|
G | A | 6 | a0001c0001t0007g0006a0001c0001t0007g0062a0001c0001t0009g0060others(3): Show | 11 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.419-95G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100450462 | ||||||
| chr9:100450491
|
G | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0161 | 3 | HG02738.hp1 HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.419-66G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100450491 |