Search by Gene
| geneid | 4292 |
|---|---|
| ensemblid | ENSG00000076242.17 |
| hgncid | 7127 |
| symbol | MLH1 |
| name | mutL homolog 1 |
| refseq_nuc | NM_000249.4 |
| refseq_prot | NP_000240.1 |
| ensembl_nuc | ENST00000231790.8 |
| ensembl_prot | ENSP00000231790.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 36993518 |
| end | 37050846 |
| strand | + |
| ver | v1.2 |
| region | chr3:36993518-37050846 |
| region5000 | chr3:36988518-37055846 |
| regionname0 | MLH1_chr3_36993518_37050846 |
| regionname5000 | MLH1_chr3_36988518_37055846 |
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 | 756 | 223 | 62 | 45 | 82 | 7 | 25 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0002 | 0/0 | 756 | 34 | 4 | 9 | 12 | 3 | 6 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0003 | 0/0 | 756 | 9 | 7 | 2 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0004 | 0/0 | 756 | 8 | 8 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0005 | 0/0 | 756 | 2 | 0 | 0 | 2 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0006 | 0/0 | 756 | 2 | 2 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0007 | 0/0 | 756 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0008 | 0/0 | 756 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0009 | 0/0 | 756 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0010 | 0/0 | 756 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2271 | 215 | 55 | 44 | 82 | 7 | 25 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| c0002 | 0/0 | 2271 | 33 | 4 | 9 | 12 | 2 | 6 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| c0003 | 0/0 | 2271 | 9 | 7 | 2 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| c0004 | 0/0 | 2271 | 8 | 8 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| c0005 | 0/0 | 2271 | 7 | 7 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| c0006 | 0/0 | 2271 | 2 | 0 | 0 | 2 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| c0007 | 0/0 | 2271 | 2 | 2 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| c0008 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| c0009 | 0/0 | 2271 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| c0010 | 0/0 | 2271 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| c0011 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| c0012 | 0/0 | 2271 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| c0013 | 0/0 | 2271 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | 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 | 1/1 | 224 | 273 | 77 | 54 | 98 | 10 | 32 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| t0002 | 0/0 | 221 | 6 | 4 | 2 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| t0003 | 0/0 | 220 | 3 | 3 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | 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 | 3 | 0 | 0 | 2 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0004 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0173 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 215 | 55 | 44 | 82 | 7 | 25 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0001c0005 | a0001 | c0005 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0001c0010 | a0001 | c0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0002c0002 | a0002 | c0002 | 0/0 | 33 | 4 | 9 | 12 | 2 | 6 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0002c0013 | a0002 | c0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0003c0003 | a0003 | c0003 | 0/0 | 9 | 7 | 2 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0004c0004 | a0004 | c0004 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0005c0006 | a0005 | c0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0006c0007 | a0006 | c0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0007c0012 | a0007 | c0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0008c0009 | a0008 | c0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0009c0011 | a0009 | c0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0010c0008 | a0010 | c0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | 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 | 1/1 | 206 | 48 | 42 | 82 | 7 | 25 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0001c0005t0001 | a0001 | c0005 | t0001 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0001c0010t0001 | a0001 | c0010 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0002c0002t0001 | a0002 | c0002 | t0001 | 0/0 | 33 | 4 | 9 | 12 | 2 | 6 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0002c0013t0001 | a0002 | c0013 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0003c0003t0001 | a0003 | c0003 | t0001 | 0/0 | 9 | 7 | 2 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0004c0004t0001 | a0004 | c0004 | t0001 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0005c0006t0001 | a0005 | c0006 | t0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0006c0007t0001 | a0006 | c0007 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0007c0012t0001 | a0007 | c0012 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0008c0009t0001 | a0008 | c0009 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0009c0011t0001 | a0009 | c0011 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | copy fasta |
| a0010c0008t0001 | a0010 | c0008 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 | 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 | 3 | 0 | 0 | 2 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0006 | a0001 | c0001 | t0001 | g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0018 | a0001 | c0001 | t0001 | g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0019 | a0001 | c0001 | t0001 | g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0020 | a0001 | c0001 | t0001 | g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0037 | a0001 | c0001 | t0001 | g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0040 | a0001 | c0001 | t0001 | g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0051 | a0001 | c0001 | t0001 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0056 | a0001 | c0001 | t0001 | g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0058 | a0001 | c0001 | t0001 | g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0104 | a0001 | c0001 | t0001 | g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0115 | a0001 | c0001 | t0001 | g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0157 | a0001 | c0001 | t0001 | g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0158 | a0001 | c0001 | t0001 | g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0164 | a0001 | c0001 | t0001 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0171 | a0001 | c0001 | t0001 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0172 | a0001 | c0001 | t0001 | g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0174 | a0001 | c0001 | t0001 | g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0175 | a0001 | c0001 | t0001 | g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0178 | a0001 | c0001 | t0001 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0179 | a0001 | c0001 | t0001 | g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0189 | a0001 | c0001 | t0001 | g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0191 | a0001 | c0001 | t0001 | g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0192 | a0001 | c0001 | t0001 | g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0193 | a0001 | c0001 | t0001 | g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0194 | a0001 | c0001 | t0001 | g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0195 | a0001 | c0001 | t0001 | g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0196 | a0001 | c0001 | t0001 | g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0207 | a0001 | c0001 | t0001 | g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0208 | a0001 | c0001 | t0001 | g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0210 | a0001 | c0001 | t0001 | g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0215 | a0001 | c0001 | t0001 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0216 | a0001 | c0001 | t0001 | g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0217 | a0001 | c0001 | t0001 | g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0218 | a0001 | c0001 | t0001 | g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0242 | a0001 | c0001 | t0001 | g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0243 | a0001 | c0001 | t0001 | g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0244 | a0001 | c0001 | t0001 | g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0245 | a0001 | c0001 | t0001 | g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0246 | a0001 | c0001 | t0001 | g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0247 | a0001 | c0001 | t0001 | g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0248 | a0001 | c0001 | t0001 | g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0249 | a0001 | c0001 | t0001 | g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0250 | a0001 | c0001 | t0001 | g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0251 | a0001 | c0001 | t0001 | g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0252 | a0001 | c0001 | t0001 | g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0253 | a0001 | c0001 | t0001 | g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0254 | a0001 | c0001 | t0001 | g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0256 | a0001 | c0001 | t0001 | g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0257 | a0001 | c0001 | t0001 | g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0001g0258 | a0001 | c0001 | t0001 | g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0002g0008 | a0001 | c0001 | t0002 | g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0002g0064 | a0001 | c0001 | t0002 | g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0002g0065 | a0001 | c0001 | t0002 | g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0002g0066 | a0001 | c0001 | t0002 | g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0002g0067 | a0001 | c0001 | t0002 | g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0003g0011 | a0001 | c0001 | t0003 | g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0001t0003g0162 | a0001 | c0001 | t0003 | g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0005t0001g0180 | a0001 | c0005 | t0001 | g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0005t0001g0181 | a0001 | c0005 | t0001 | g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0005t0001g0182 | a0001 | c0005 | t0001 | g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0005t0001g0183 | a0001 | c0005 | t0001 | g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0005t0001g0184 | a0001 | c0005 | t0001 | g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0005t0001g0185 | a0001 | c0005 | t0001 | g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0005t0001g0186 | a0001 | c0005 | t0001 | g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0001c0010t0001g0027 | a0001 | c0010 | t0001 | g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0004 | a0002 | c0002 | t0001 | g0004 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0013 | a0002 | c0002 | t0001 | g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0014 | a0002 | c0002 | t0001 | g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0202 | a0002 | c0002 | t0001 | g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0203 | a0002 | c0002 | t0001 | g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0204 | a0002 | c0002 | t0001 | g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0205 | a0002 | c0002 | t0001 | g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0206 | a0002 | c0002 | t0001 | g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0209 | a0002 | c0002 | t0001 | g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0211 | a0002 | c0002 | t0001 | g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0219 | a0002 | c0002 | t0001 | g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0220 | a0002 | c0002 | t0001 | g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0221 | a0002 | c0002 | t0001 | g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0222 | a0002 | c0002 | t0001 | g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0223 | a0002 | c0002 | t0001 | g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0224 | a0002 | c0002 | t0001 | g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0225 | a0002 | c0002 | t0001 | g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0226 | a0002 | c0002 | t0001 | g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0227 | a0002 | c0002 | t0001 | g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0228 | a0002 | c0002 | t0001 | g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0229 | a0002 | c0002 | t0001 | g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0230 | a0002 | c0002 | t0001 | g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0231 | a0002 | c0002 | t0001 | g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0232 | a0002 | c0002 | t0001 | g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0233 | a0002 | c0002 | t0001 | g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0234 | a0002 | c0002 | t0001 | g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0235 | a0002 | c0002 | t0001 | g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0236 | a0002 | c0002 | t0001 | g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0002t0001g0255 | a0002 | c0002 | t0001 | g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0002c0013t0001g0237 | a0002 | c0013 | t0001 | g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0003c0003t0001g0015 | a0003 | c0003 | t0001 | g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0003c0003t0001g0212 | a0003 | c0003 | t0001 | g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0003c0003t0001g0213 | a0003 | c0003 | t0001 | g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0003c0003t0001g0214 | a0003 | c0003 | t0001 | g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0003c0003t0001g0238 | a0003 | c0003 | t0001 | g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0003c0003t0001g0239 | a0003 | c0003 | t0001 | g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0003c0003t0001g0240 | a0003 | c0003 | t0001 | g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0003c0003t0001g0241 | a0003 | c0003 | t0001 | g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0004c0004t0001g0024 | a0004 | c0004 | t0001 | g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0004c0004t0001g0187 | a0004 | c0004 | t0001 | g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0004c0004t0001g0188 | a0004 | c0004 | t0001 | g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0004c0004t0001g0197 | a0004 | c0004 | t0001 | g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0004c0004t0001g0198 | a0004 | c0004 | t0001 | g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0004c0004t0001g0199 | a0004 | c0004 | t0001 | g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0004c0004t0001g0200 | a0004 | c0004 | t0001 | g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0004c0004t0001g0201 | a0004 | c0004 | t0001 | g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0005c0006t0001g0006 | a0005 | c0006 | t0001 | g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0005c0006t0001g0054 | a0005 | c0006 | t0001 | g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0006c0007t0001g0176 | a0006 | c0007 | t0001 | g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0006c0007t0001g0177 | a0006 | c0007 | t0001 | g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0007c0012t0001g0113 | a0007 | c0012 | t0001 | g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0008c0009t0001g0190 | a0008 | c0009 | t0001 | g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0009c0011t0001g0073 | a0009 | c0011 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| a0010c0008t0001g0142 | a0010 | c0008 | t0001 | g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLH1_chr3_36988518_37055846 | MLH1 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0235 | EUR | GBR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | GBR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | GBR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | FIN | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | FIN | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | CHS | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0219 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0211 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00741 | hp1 | a0003 | c0003 | t0001 | g0213 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0222 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0225 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0231 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0240 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0226 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0220 | AMR | CLM | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01346 | hp2 | a0001 | c0010 | t0001 | g0027 | AMR | CLM | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | IBS | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01517 | hp2 | a0002 | c0013 | t0001 | g0237 | EUR | IBS | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0221 | AMR | PEL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02055 | hp1 | a0003 | c0003 | t0001 | g0212 | AFR | ACB | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02145 | hp2 | a0006 | c0007 | t0001 | g0176 | AFR | ACB | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0202 | AMR | PEL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0234 | AFR | ACB | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02257 | hp2 | a0001 | c0005 | t0001 | g0180 | AFR | ACB | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02258 | hp1 | a0004 | c0004 | t0001 | g0201 | AFR | ACB | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | ACB | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02280 | hp2 | a0001 | c0005 | t0001 | g0181 | AFR | ACB | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02622 | hp2 | a0004 | c0004 | t0001 | g0199 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0224 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02809 | hp2 | a0001 | c0005 | t0001 | g0184 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02886 | hp1 | a0008 | c0009 | t0001 | g0190 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02895 | hp2 | a0003 | c0003 | t0001 | g0015 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02896 | hp1 | a0004 | c0004 | t0001 | g0197 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0015 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02897 | hp2 | a0004 | c0004 | t0001 | g0198 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02922 | hp2 | a0001 | c0005 | t0001 | g0185 | AFR | ESN | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02970 | hp1 | a0003 | c0003 | t0001 | g0239 | AFR | ESN | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03098 | hp1 | a0004 | c0004 | t0001 | g0187 | AFR | MSL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | MSL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0232 | AFR | ESN | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | MSL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03225 | hp1 | a0001 | c0005 | t0001 | g0182 | AFR | MSL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | MSL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03453 | hp2 | a0001 | c0005 | t0001 | g0186 | AFR | MSL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03486 | hp2 | a0001 | c0005 | t0001 | g0183 | AFR | MSL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03540 | hp1 | a0004 | c0004 | t0001 | g0024 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03579 | hp2 | a0004 | c0004 | t0001 | g0188 | AFR | MSL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0205 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03834 | hp1 | a0007 | c0012 | t0001 | g0113 | SAS | BEB | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | MLH1_chr3_36988518_37055846 | MLH1 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | MLH1_chr3_36988518_37055846 | MLH1 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | STU | MLH1_chr3_36988518_37055846 | MLH1 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | STU | MLH1_chr3_36988518_37055846 | MLH1 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | STU | MLH1_chr3_36988518_37055846 | MLH1 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0206 | SAS | STU | MLH1_chr3_36988518_37055846 | MLH1 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0203 | SAS | STU | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | YRI | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHB | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHB | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18964 | hp2 | a0010 | c0008 | t0001 | g0142 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18969 | hp2 | a0005 | c0006 | t0001 | g0006 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18986 | hp2 | a0005 | c0006 | t0001 | g0054 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19030 | hp1 | a0003 | c0003 | t0001 | g0214 | AFR | LWK | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | LWK | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19043 | hp1 | a0006 | c0007 | t0001 | g0177 | AFR | LWK | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19043 | hp2 | a0004 | c0004 | t0001 | g0200 | AFR | LWK | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19063 | hp1 | a0009 | c0011 | t0001 | g0073 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | TSI | MLH1_chr3_36988518_37055846 | MLH1 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0204 | EUR | TSI | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | MLH1_chr3_36988518_37055846 | MLH1 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02559 | hp1 | a0003 | c0003 | t0001 | g0241 | AFR | ACB | MLH1_chr3_36988518_37055846 | MLH1 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | MLH1_chr3_36988518_37055846 | MLH1 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | USA | MLH1_chr3_36988518_37055846 | MLH1 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | USA | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MLH1_chr3_36988518_37055846 | MLH1 |
| NA20300 | hp1 | a0003 | c0003 | t0001 | g0238 | AFR | USA | MLH1_chr3_36988518_37055846 | MLH1 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | USA | MLH1_chr3_36988518_37055846 | MLH1 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0236 | AFR | LWK | MLH1_chr3_36988518_37055846 | MLH1 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | MLH1_chr3_36988518_37055846 | MLH1 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0042 | REF | REF | MLH1_chr3_36988518_37055846 | MLH1 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0173 | REF | REF | MLH1_chr3_36988518_37055846 | MLH1 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:37001011
|
T | G | 1 | a0010 | 1 | NA18964.hp2 | missense_variant | MODERATE | c.264T>G | p.Phe88Leu | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/19 | 294/2494 | 264/2271 | 88/756 | chr3 | 37001011 | ||
| chr3:37012059
|
G | A | 1 | a0004 | 8 | HG02258.hp1 HG02622.hp2 HG02896.hp1 others(5): Show |
missense_variant | MODERATE | c.637G>A | p.Val213Met | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 8/19 | 667/2494 | 637/2271 | 213/756 | chr3 | 37012059 | ||
| chr3:37012071
|
C | T | 1 | a0007 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.649C>T | p.Arg217Cys | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 8/19 | 679/2494 | 649/2271 | 217/756 | chr3 | 37012071 | ||
| chr3:37012077
|
A | G | 1 | a0002 | 34 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(31): Show |
missense_variant | MODERATE | c.655A>G | p.Ile219Val | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 8/19 | 685/2494 | 655/2271 | 219/756 | chr3 | 37012077 | ||
| chr3:37025749
|
T | A | 1 | a0005 | 2 | NA18969.hp2 NA18986.hp2 |
missense_variant | MODERATE | c.1151T>A | p.Val384Asp | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/19 | 1181/2494 | 1151/2271 | 384/756 | chr3 | 37025749 | ||
| chr3:37047531
|
C | G | 1 | a0009 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.1744C>G | p.Leu582Val | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 16/19 | 1774/2494 | 1744/2271 | 582/756 | chr3 | 37047531 | ||
| chr3:37048583
|
A | G | 1 | a0006 | 2 | HG02145.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.1963A>G | p.Ile655Val | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 17/19 | 1993/2494 | 1963/2271 | 655/756 | chr3 | 37048583 | ||
| chr3:37050534
|
C | T | 1 | a0003 | 9 | HG00741.hp1 HG01109.hp1 HG02055.hp1 others(6): Show |
missense_variant | MODERATE | c.2152C>T | p.His718Tyr | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 19/19 | 2182/2494 | 2152/2271 | 718/756 | chr3 | 37050534 | ||
| chr3:37050595
|
G | A | 1 | a0008 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.2213G>A | p.Gly738Glu | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 19/19 | 2243/2494 | 2213/2271 | 738/756 | chr3 | 37050595 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:37004469
|
A | G | 1 | a0002c0013 | 1 | HG01517.hp2 | synonymous_variant | LOW | c.375A>G | p.Ala125Ala | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/19 | 405/2494 | 375/2271 | 125/756 | chr3 | 37004469 | ||
| chr3:37008834
|
C | T | 1 | a0001c0005 | 7 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(4): Show |
synonymous_variant | LOW | c.474C>T | p.Asn158Asn | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/19 | 504/2494 | 474/2271 | 158/756 | chr3 | 37008834 | ||
| chr3:37048579
|
G | T | 1 | a0001c0010 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.1959G>T | p.Leu653Leu | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 17/19 | 1989/2494 | 1959/2271 | 653/756 | chr3 | 37048579 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:37050682
|
GTTC | G | 1 | a0001c0001t0002 | 6 | HG01074.hp2 HG01099.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*35_*37delCTT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 19/19 | 35 | INFO_REALIGN_3_PRIME | chr3 | 37050682 | ||||
| chr3:37050810
|
GGATT | G | 1 | a0001c0001t0003 | 3 | HG02258.hp2 NA19030.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*162_*165delGATT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 19/19 | 162 | INFO_REALIGN_3_PRIME | chr3 | 37050810 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:36993883
|
T | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02735.hp2 HG03471.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+220T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36993883 | ||||||
| chr3:36993971
|
T | A | 1 | a0001c0001t0001g0025 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.116+308T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36993971 | ||||||
| chr3:36994016
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.116+353G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36994016 | ||||||
| chr3:36994017
|
A | G | 1 | a0001c0001t0001g0025 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.116+354A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36994017 | ||||||
| chr3:36994018
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.116+355G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36994018 | ||||||
| chr3:36994020
|
A | G | 1 | a0001c0001t0001g0258 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.116+357A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36994020 | ||||||
| chr3:36994185
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.116+522C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36994185 | ||||||
| chr3:36994242
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.116+579C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36994242 | ||||||
| chr3:36994314
|
A | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02735.hp2 HG03471.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+651A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36994314 | ||||||
| chr3:36994343
|
A | G | 65 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 77 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.116+680A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36994343 | ||||||
| chr3:36994608
|
A | AG | 84 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(81): Show | 96 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.116+946dupG | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 36994608 | |||||
| chr3:36994723
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.116+1060T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36994723 | ||||||
| chr3:36994800
|
ATTTTTAT others(4): Show |
A | 5 | a0001c0001t0001g0189a0001c0001t0001g0191a0004c0004t0001g0187others(2): Show | 5 | HG02717.hp2 HG02886.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+1155_116+1165d others(13): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 36994800 | |||||
| chr3:36994806
|
A | T | 2 | a0001c0001t0001g0023a0004c0004t0001g0024 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.116+1143A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36994806 | ||||||
| chr3:36994810
|
T | A | 21 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0029others(18): Show | 22 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.116+1147T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36994810 | ||||||
| chr3:36994817
|
A | T | 1 | a0004c0004t0001g0024 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.116+1154A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36994817 | ||||||
| chr3:36994951
|
T | C | 1 | a0002c0002t0001g0202 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.116+1288T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36994951 | ||||||
| chr3:36995022
|
C | T | 7 | a0001c0005t0001g0180a0001c0005t0001g0181a0001c0005t0001g0182others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.116+1359C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36995022 | ||||||
| chr3:36995193
|
G | A | 14 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0046others(11): Show | 16 | HG00140.hp1 HG01517.hp1 HG02148.hp2 others(13): Show |
intron_variant | MODIFIER | c.117-1426G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36995193 | ||||||
| chr3:36995235
|
C | T | 3 | a0001c0001t0001g0189a0001c0001t0001g0191a0008c0009t0001g0190 | 3 | HG02717.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.117-1384C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36995235 | ||||||
| chr3:36995238
|
G | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02735.hp2 HG03471.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-1381G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36995238 | ||||||
| chr3:36995393
|
A | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG02735.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.117-1226A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36995393 | ||||||
| chr3:36995493
|
G | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02735.hp2 HG03471.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-1126G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36995493 | ||||||
| chr3:36995576
|
C | T | 7 | a0004c0004t0001g0187a0004c0004t0001g0188a0004c0004t0001g0197others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.117-1043C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36995576 | ||||||
| chr3:36995577
|
G | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02735.hp2 HG03471.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-1042G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36995577 | ||||||
| chr3:36995761
|
G | A | 4 | a0001c0005t0001g0180a0001c0005t0001g0181a0001c0005t0001g0182others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-858G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36995761 | ||||||
| chr3:36995813
|
T | TC | 11 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(8): Show | 11 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.117-805dupC | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 36995813 | |||||
| chr3:36995815
|
T | C | 1 | a0004c0004t0001g0197 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.117-804T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36995815 | ||||||
| chr3:36995823
|
G | T | 1 | a0004c0004t0001g0197 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.117-796G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36995823 | ||||||
| chr3:36995825
|
GT | G | 12 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(9): Show | 13 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.117-779delT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 36995825 | |||||
| chr3:36995826
|
T | G | 1 | a0004c0004t0001g0197 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.117-793T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36995826 | ||||||
| chr3:36995827
|
T | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02735.hp2 HG03471.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-792T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36995827 | ||||||
| chr3:36995870
|
T | A | 1 | a0001c0001t0001g0257 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.117-749T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36995870 | ||||||
| chr3:36995884
|
C | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.117-735C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36995884 | ||||||
| chr3:36996035
|
C | G | 1 | a0001c0001t0001g0254 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.117-584C>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36996035 | ||||||
| chr3:36996086
|
G | C | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.117-533G>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36996086 | ||||||
| chr3:36996225
|
G | A | 5 | a0001c0001t0002g0008a0001c0001t0002g0064a0001c0001t0002g0065others(2): Show | 6 | HG01074.hp2 HG01099.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.117-394G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36996225 | ||||||
| chr3:36996453
|
A | G | 1 | a0001c0005t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.117-166A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36996453 | ||||||
| chr3:36996502
|
C | T | 2 | a0006c0007t0001g0176a0006c0007t0001g0177 | 2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.117-117C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36996502 | ||||||
| chr3:36996609
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.117-10G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 1/18 | chr3 | 36996609 | ||||||
| chr3:36996982
|
T | G | 1 | a0002c0002t0001g0203 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.207+273T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 36996982 | ||||||
| chr3:36997280
|
C | T | 84 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(81): Show | 96 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.207+571C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 36997280 | ||||||
| chr3:36997288
|
C | G | 3 | a0001c0001t0001g0189a0001c0001t0001g0191a0008c0009t0001g0190 | 3 | HG02717.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.207+579C>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 36997288 | ||||||
| chr3:36997295
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.207+586G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 36997295 | ||||||
| chr3:36997625
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.207+916A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 36997625 | ||||||
| chr3:36997861
|
T | C | 1 | a0002c0002t0001g0204 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.207+1152T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 36997861 | ||||||
| chr3:36997973
|
G | A | 3 | a0001c0001t0002g0008a0001c0001t0002g0064a0001c0001t0002g0065 | 4 | HG01074.hp2 HG01099.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+1264G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 36997973 | ||||||
| chr3:36998047
|
G | A | 2 | a0002c0002t0001g0205a0002c0002t0001g0206 | 2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.207+1338G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 36998047 | ||||||
| chr3:36998070
|
C | CA | 32 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(29): Show | 32 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.207+1387dupA | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 36998070 | |||||
| chr3:36998070
|
CA | C | 77 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(74): Show | 88 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.207+1387delA | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 36998070 | |||||
| chr3:36998435
|
T | G | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.207+1726T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 36998435 | ||||||
| chr3:36998604
|
C | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02735.hp2 HG03471.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+1895C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 36998604 | ||||||
| chr3:36998735
|
A | T | 1 | a0002c0002t0001g0206 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.207+2026A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 36998735 | ||||||
| chr3:36998837
|
T | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02735.hp2 HG03471.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-2118T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 36998837 | ||||||
| chr3:36998863
|
T | A | 1 | a0001c0001t0002g0066 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.208-2092T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 36998863 | ||||||
| chr3:36999213
|
G | A | 7 | a0004c0004t0001g0187a0004c0004t0001g0188a0004c0004t0001g0197others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-1742G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 36999213 | ||||||
| chr3:36999257
|
T | C | 65 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 77 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.208-1698T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 36999257 | ||||||
| chr3:36999295
|
G | A | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(254): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.208-1660G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 36999295 | ||||||
| chr3:36999519
|
C | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02735.hp2 HG03471.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-1436C>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 36999519 | ||||||
| chr3:36999541
|
A | AT | 84 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(81): Show | 96 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.208-1414_208-1413i others(3): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 36999541 | ||||||
| chr3:36999829
|
C | A | 65 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 77 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.208-1126C>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 36999829 | ||||||
| chr3:37000203
|
G | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0191a0008c0009t0001g0190 | 3 | HG02717.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.208-752G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 37000203 | ||||||
| chr3:37000314
|
G | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0058 | 3 | HG01167.hp2 HG01169.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.208-641G>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 37000314 | ||||||
| chr3:37000336
|
A | AGTCCCAG others(66): Show |
1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.208-617_208-545dup others(73): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 37000336 | |||||
| chr3:37000557
|
C | T | 3 | a0001c0001t0001g0189a0001c0001t0001g0191a0008c0009t0001g0190 | 3 | HG02717.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.208-398C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 37000557 | ||||||
| chr3:37000591
|
A | G | 84 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(81): Show | 96 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.208-364A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 37000591 | ||||||
| chr3:37000804
|
C | CA | 8 | a0001c0001t0001g0032a0001c0001t0001g0070a0001c0001t0001g0088others(5): Show | 8 | HG01496.hp1 HG02055.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.208-137dupA | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 37000804 | |||||
| chr3:37000804
|
CA | C | 11 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(8): Show | 11 | HG01168.hp1 HG01358.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.208-137delA | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 37000804 | |||||
| chr3:37000817
|
A | C | 1 | a0001c0001t0001g0194 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.208-138A>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 37000817 | ||||||
| chr3:37000846
|
C | A | 1 | a0002c0002t0001g0206 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.208-109C>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 2/18 | chr3 | 37000846 | ||||||
| chr3:37001266
|
T | C | 2 | a0002c0002t0001g0219a0002c0002t0001g0220 | 2 | HG00639.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.306+213T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37001266 | ||||||
| chr3:37001267
|
A | G | 1 | a0001c0001t0001g0253 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.306+214A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37001267 | ||||||
| chr3:37001469
|
A | C | 65 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 77 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.306+416A>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37001469 | ||||||
| chr3:37001518
|
A | C | 2 | a0002c0002t0001g0219a0002c0002t0001g0220 | 2 | HG00639.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.306+465A>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37001518 | ||||||
| chr3:37001672
|
G | GT | 28 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(25): Show | 35 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.306+630dupT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr3 | 37001672 | |||||
| chr3:37001727
|
A | T | 1 | a0001c0001t0002g0008 | 2 | HG01074.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.306+674A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37001727 | ||||||
| chr3:37001739
|
G | A | 85 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(82): Show | 97 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.306+686G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37001739 | ||||||
| chr3:37001765
|
G | A | 12 | a0001c0001t0002g0008a0001c0001t0002g0064a0001c0001t0002g0065others(9): Show | 13 | HG01074.hp2 HG01099.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.306+712G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37001765 | ||||||
| chr3:37001778
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.306+725A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37001778 | ||||||
| chr3:37001952
|
G | GT | 13 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(10): Show | 13 | HG00738.hp2 HG00741.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.306+910dupT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr3 | 37001952 | |||||
| chr3:37001952
|
GT | G | 81 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(78): Show | 94 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.306+910delT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr3 | 37001952 | |||||
| chr3:37001953
|
T | G | 1 | a0001c0001t0001g0091 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.306+900T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37001953 | ||||||
| chr3:37001963
|
T | G | 9 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0005t0001g0180others(6): Show | 9 | HG01934.hp1 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.306+910T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37001963 | ||||||
| chr3:37001964
|
G | GT | 9 | a0001c0001t0001g0007a0001c0001t0001g0058a0001c0001t0001g0085others(6): Show | 11 | HG01106.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.306+926dupT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr3 | 37001964 | |||||
| chr3:37001964
|
G | T | 10 | a0001c0001t0001g0044a0001c0001t0001g0194a0001c0001t0001g0196others(7): Show | 10 | HG01934.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.306+911G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37001964 | ||||||
| chr3:37001965
|
T | G | 2 | a0001c0001t0001g0023a0004c0004t0001g0024 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.306+912T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37001965 | ||||||
| chr3:37001968
|
T | G | 65 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 77 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.306+915T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37001968 | ||||||
| chr3:37002015
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.306+962A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37002015 | ||||||
| chr3:37002257
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | NA18747.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.306+1204G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37002257 | ||||||
| chr3:37002305
|
G | A | 14 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(11): Show | 14 | HG00738.hp2 HG00741.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.306+1252G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37002305 | ||||||
| chr3:37002474
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.306+1421G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37002474 | ||||||
| chr3:37002544
|
A | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02735.hp2 HG03471.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+1491A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37002544 | ||||||
| chr3:37002820
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02735.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.307-1581A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37002820 | ||||||
| chr3:37002838
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.307-1563C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37002838 | ||||||
| chr3:37002888
|
C | G | 8 | a0003c0003t0001g0015a0003c0003t0001g0212a0003c0003t0001g0213others(5): Show | 9 | HG00741.hp1 HG01109.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.307-1513C>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37002888 | ||||||
| chr3:37002946
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.307-1455C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37002946 | ||||||
| chr3:37002982
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.307-1419A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37002982 | ||||||
| chr3:37002998
|
A | T | 46 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(43): Show | 49 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.307-1403A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37002998 | ||||||
| chr3:37003030
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-1371G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37003030 | ||||||
| chr3:37003101
|
T | C | 2 | a0001c0001t0001g0023a0004c0004t0001g0024 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.307-1300T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37003101 | ||||||
| chr3:37003211
|
C | A | 7 | a0001c0005t0001g0180a0001c0005t0001g0181a0001c0005t0001g0182others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.307-1190C>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37003211 | ||||||
| chr3:37003271
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.307-1130G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37003271 | ||||||
| chr3:37003352
|
C | CT | 11 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(8): Show | 11 | HG00735.hp2 HG01517.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.307-1031dupT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr3 | 37003352 | |||||
| chr3:37003352
|
CT | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0033a0001c0001t0001g0035others(5): Show | 9 | HG01496.hp2 HG01952.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.307-1031delT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr3 | 37003352 | |||||
| chr3:37003672
|
A | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG01255.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.307-729A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37003672 | ||||||
| chr3:37003677
|
A | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0058 | 3 | HG01167.hp2 HG01169.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.307-724A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37003677 | ||||||
| chr3:37003739
|
G | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.307-662G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37003739 | ||||||
| chr3:37003742
|
A | C | 84 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(81): Show | 96 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.307-659A>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37003742 | ||||||
| chr3:37004372
|
C | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02735.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.307-29C>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37004372 | ||||||
| chr3:37004377
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.307-24A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 3/18 | chr3 | 37004377 | ||||||
| chr3:37004594
|
G | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02735.hp2 HG03471.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.380+120G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37004594 | ||||||
| chr3:37004638
|
A | G | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.380+164A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37004638 | ||||||
| chr3:37004740
|
A | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0175 | 2 | HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.380+266A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37004740 | ||||||
| chr3:37004883
|
T | A | 1 | a0001c0001t0001g0046 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.380+409T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37004883 | ||||||
| chr3:37004931
|
T | C | 7 | a0004c0004t0001g0187a0004c0004t0001g0188a0004c0004t0001g0197others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.380+457T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37004931 | ||||||
| chr3:37004964
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.380+490C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37004964 | ||||||
| chr3:37005096
|
CACACAGG others(19): Show |
C | 1 | a0001c0001t0001g0252 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.380+623_380+648del others(26): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37005096 | ||||||
| chr3:37005167
|
C | G | 2 | a0001c0001t0001g0023a0004c0004t0001g0024 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.380+693C>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37005167 | ||||||
| chr3:37005228
|
C | T | 12 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(9): Show | 12 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.380+754C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37005228 | ||||||
| chr3:37005232
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.380+758G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37005232 | ||||||
| chr3:37005264
|
G | A | 1 | a0002c0002t0001g0203 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.380+790G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37005264 | ||||||
| chr3:37005308
|
G | T | 1 | a0002c0002t0001g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380+834G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37005308 | ||||||
| chr3:37005309
|
A | T | 1 | a0002c0002t0001g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380+835A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37005309 | ||||||
| chr3:37005603
|
T | A | 7 | a0004c0004t0001g0187a0004c0004t0001g0188a0004c0004t0001g0197others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.380+1129T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37005603 | ||||||
| chr3:37005741
|
C | T | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(1): Show | 4 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.381-1250C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37005741 | ||||||
| chr3:37005900
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.381-1091C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37005900 | ||||||
| chr3:37005942
|
G | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.381-1049G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37005942 | ||||||
| chr3:37006053
|
A | G | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.381-938A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37006053 | ||||||
| chr3:37006092
|
A | G | 84 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(81): Show | 96 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.381-899A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37006092 | ||||||
| chr3:37006127
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.381-864T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37006127 | ||||||
| chr3:37006220
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0057a0001c0001t0001g0058others(7): Show | 11 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.381-771C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37006220 | ||||||
| chr3:37006286
|
G | A | 65 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 77 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.381-705G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37006286 | ||||||
| chr3:37006324
|
G | A | 1 | a0003c0003t0001g0015 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.381-667G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37006324 | ||||||
| chr3:37006401
|
G | A | 7 | a0001c0005t0001g0180a0001c0005t0001g0181a0001c0005t0001g0182others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.381-590G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37006401 | ||||||
| chr3:37006437
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.381-554A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37006437 | ||||||
| chr3:37006450
|
T | C | 1 | a0001c0001t0001g0079 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.381-541T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37006450 | ||||||
| chr3:37006576
|
C | T | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.381-415C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37006576 | ||||||
| chr3:37006782
|
C | T | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.381-209C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37006782 | ||||||
| chr3:37006868
|
ATAAT | A | 7 | a0004c0004t0001g0187a0004c0004t0001g0188a0004c0004t0001g0197others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.381-119_381-116del others(4): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 37006868 | |||||
| chr3:37006950
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.381-41A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 4/18 | chr3 | 37006950 | ||||||
| chr3:37007088
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02735.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.453+25A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 5/18 | chr3 | 37007088 | ||||||
| chr3:37007142
|
A | G | 84 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(81): Show | 96 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.453+79A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 5/18 | chr3 | 37007142 | ||||||
| chr3:37007251
|
C | T | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.453+188C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 5/18 | chr3 | 37007251 | ||||||
| chr3:37007255
|
C | T | 5 | a0001c0001t0001g0087a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG01168.hp1 HG02647.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.453+192C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 5/18 | chr3 | 37007255 | ||||||
| chr3:37007607
|
T | C | 69 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(66): Show | 81 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.453+544T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 5/18 | chr3 | 37007607 | ||||||
| chr3:37007718
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0057a0001c0001t0001g0058others(7): Show | 11 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.453+655G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 5/18 | chr3 | 37007718 | ||||||
| chr3:37007829
|
C | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.453+766C>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 5/18 | chr3 | 37007829 | ||||||
| chr3:37007848
|
A | C | 2 | a0001c0001t0001g0083a0001c0001t0001g0157 | 2 | NA19010.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.453+785A>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 5/18 | chr3 | 37007848 | ||||||
| chr3:37007891
|
C | T | 3 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | HG00280.hp1 HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.453+828C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 5/18 | chr3 | 37007891 | ||||||
| chr3:37007956
|
C | T | 2 | a0006c0007t0001g0176a0006c0007t0001g0177 | 2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.454-858C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 5/18 | chr3 | 37007956 | ||||||
| chr3:37007957
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0166 | 2 | HG01106.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.454-857G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 5/18 | chr3 | 37007957 | ||||||
| chr3:37008040
|
A | G | 1 | a0008c0009t0001g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.454-774A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 5/18 | chr3 | 37008040 | ||||||
| chr3:37008084
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02735.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.454-730G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 5/18 | chr3 | 37008084 | ||||||
| chr3:37008146
|
C | CT | 8 | a0001c0001t0001g0087a0001c0001t0001g0159a0001c0001t0001g0167others(5): Show | 8 | HG00597.hp1 HG01168.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.454-655dupT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr3 | 37008146 | |||||
| chr3:37008439
|
G | T | 1 | a0001c0005t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.454-375G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 5/18 | chr3 | 37008439 | ||||||
| chr3:37008763
|
T | C | 5 | a0001c0001t0002g0008a0001c0001t0002g0064a0001c0001t0002g0065others(2): Show | 6 | HG01074.hp2 HG01099.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.454-51T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 5/18 | chr3 | 37008763 | ||||||
| chr3:37008925
|
A | T | 3 | a0001c0001t0001g0189a0001c0001t0001g0191a0008c0009t0001g0190 | 3 | HG02717.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.545+20A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37008925 | ||||||
| chr3:37009493
|
C | A | 1 | a0002c0002t0001g0204 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.545+588C>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37009493 | ||||||
| chr3:37009599
|
AGTGTATA others(49): Show |
A | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG00099.hp2 HG00280.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.545+713_545+768del others(56): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr3 | 37009599 | |||||
| chr3:37009633
|
T | C | 12 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(9): Show | 12 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.545+728T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37009633 | ||||||
| chr3:37009640
|
G | GTA | 84 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(81): Show | 96 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.545+745_545+746dup others(2): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr3 | 37009640 | |||||
| chr3:37009646
|
ATATATGT others(5): Show |
A | 12 | a0001c0001t0002g0008a0001c0001t0002g0064a0001c0001t0002g0065others(9): Show | 13 | HG01074.hp2 HG01099.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.545+747_545+758del others(12): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr3 | 37009646 | |||||
| chr3:37009658
|
GTATATAT others(15): Show |
G | 27 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(24): Show | 28 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.545+819_545+840del others(22): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr3 | 37009658 | |||||
| chr3:37009658
|
GTATATAT others(37): Show |
G | 66 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(63): Show | 78 | HG00544.hp2 HG00639.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.545+797_545+840del others(44): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr3 | 37009658 | |||||
| chr3:37009670
|
A | G | 12 | a0001c0001t0002g0008a0001c0001t0002g0064a0001c0001t0002g0065others(9): Show | 13 | HG01074.hp2 HG01099.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.545+765A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37009670 | ||||||
| chr3:37009672
|
GTATATAT others(1): Show |
G | 12 | a0001c0001t0002g0008a0001c0001t0002g0064a0001c0001t0002g0065others(9): Show | 13 | HG01074.hp2 HG01099.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.545+775_545+782del others(8): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr3 | 37009672 | |||||
| chr3:37009682
|
ATATATGT others(21): Show |
A | 2 | a0001c0001t0001g0023a0004c0004t0001g0024 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.545+789_545+816del others(28): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr3 | 37009682 | |||||
| chr3:37009698
|
ATATTTAT others(5): Show |
A | 2 | a0002c0002t0001g0234a0002c0002t0001g0235 | 2 | HG00099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.545+797_545+808del others(12): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr3 | 37009698 | |||||
| chr3:37009704
|
ATATATGT others(21): Show |
A | 14 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(11): Show | 14 | HG00738.hp2 HG00741.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.545+811_545+838del others(28): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr3 | 37009704 | |||||
| chr3:37009716
|
G | T | 2 | a0002c0002t0001g0234a0002c0002t0001g0235 | 2 | HG00099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.545+811G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37009716 | ||||||
| chr3:37009724
|
T | G | 2 | a0002c0002t0001g0234a0002c0002t0001g0235 | 2 | HG00099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.545+819T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37009724 | ||||||
| chr3:37009730
|
A | G | 2 | a0002c0002t0001g0234a0002c0002t0001g0235 | 2 | HG00099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.545+825A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37009730 | ||||||
| chr3:37009734
|
A | G | 2 | a0002c0002t0001g0234a0002c0002t0001g0235 | 2 | HG00099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.545+829A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37009734 | ||||||
| chr3:37009736
|
A | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG01255.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.545+831A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37009736 | ||||||
| chr3:37009746
|
A | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.545+841A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37009746 | ||||||
| chr3:37009756
|
G | A | 2 | a0002c0002t0001g0234a0002c0002t0001g0235 | 2 | HG00099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.545+851G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37009756 | ||||||
| chr3:37009758
|
A | G | 2 | a0002c0002t0001g0234a0002c0002t0001g0235 | 2 | HG00099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.545+853A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37009758 | ||||||
| chr3:37009762
|
G | A | 2 | a0002c0002t0001g0234a0002c0002t0001g0235 | 2 | HG00099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.545+857G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37009762 | ||||||
| chr3:37009768
|
A | G | 18 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(15): Show | 18 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.545+863A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37009768 | ||||||
| chr3:37009800
|
A | G | 2 | a0001c0001t0001g0023a0004c0004t0001g0024 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.545+895A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37009800 | ||||||
| chr3:37009810
|
A | T | 1 | a0001c0001t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.545+905A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37009810 | ||||||
| chr3:37009812
|
T | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0059a0002c0002t0001g0255others(1): Show | 4 | HG03471.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+907T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37009812 | ||||||
| chr3:37009833
|
G | A | 12 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(9): Show | 12 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.545+928G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37009833 | ||||||
| chr3:37009866
|
G | A | 7 | a0004c0004t0001g0187a0004c0004t0001g0188a0004c0004t0001g0197others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.545+961G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37009866 | ||||||
| chr3:37009984
|
T | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG01255.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.545+1079T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37009984 | ||||||
| chr3:37010051
|
T | C | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.545+1146T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37010051 | ||||||
| chr3:37010055
|
T | C | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.545+1150T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37010055 | ||||||
| chr3:37010123
|
C | CT | 31 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0056others(28): Show | 33 | HG00544.hp2 HG00741.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.545+1246dupT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr3 | 37010123 | |||||
| chr3:37010123
|
C | CTTTT | 9 | a0001c0001t0001g0022a0001c0001t0001g0192a0001c0001t0001g0193others(6): Show | 9 | HG01884.hp2 HG01934.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.545+1243_545+1246d others(6): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr3 | 37010123 | |||||
| chr3:37010123
|
CT | C | 93 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(90): Show | 97 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.545+1246delT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr3 | 37010123 | |||||
| chr3:37010123
|
CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0001g0023a0004c0004t0001g0024 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.545+1231_545+1246d others(18): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr3 | 37010123 | |||||
| chr3:37010134
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.545+1229T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37010134 | ||||||
| chr3:37010176
|
A | C | 120 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0016others(117): Show | 134 | HG00099.hp1 HG00544.hp2 HG00639.hp1 others(131): Show |
intron_variant | MODIFIER | c.545+1271A>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37010176 | ||||||
| chr3:37010296
|
C | T | 8 | a0003c0003t0001g0214a0004c0004t0001g0187a0004c0004t0001g0188others(5): Show | 8 | HG02258.hp1 HG02622.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.545+1391C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37010296 | ||||||
| chr3:37010396
|
G | A | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.546-1424G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37010396 | ||||||
| chr3:37010460
|
T | C | 5 | a0001c0001t0002g0008a0001c0001t0002g0064a0001c0001t0002g0065others(2): Show | 6 | HG01074.hp2 HG01099.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.546-1360T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37010460 | ||||||
| chr3:37010491
|
G | A | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.546-1329G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37010491 | ||||||
| chr3:37010579
|
T | C | 84 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(81): Show | 96 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.546-1241T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37010579 | ||||||
| chr3:37010609
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.546-1211C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37010609 | ||||||
| chr3:37010706
|
A | AT | 12 | a0001c0001t0001g0025a0001c0001t0001g0056a0001c0001t0001g0070others(9): Show | 12 | HG00738.hp1 HG01934.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.546-1098dupT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr3 | 37010706 | |||||
| chr3:37011021
|
GAAAT | G | 3 | a0001c0001t0001g0069a0001c0001t0001g0132a0001c0001t0001g0175 | 3 | HG02615.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.546-796_546-793del others(4): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr3 | 37011021 | |||||
| chr3:37011027
|
A | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0132a0001c0001t0001g0175 | 3 | HG02615.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.546-793A>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37011027 | ||||||
| chr3:37011152
|
T | A | 2 | a0001c0001t0001g0023a0004c0004t0001g0024 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.546-668T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37011152 | ||||||
| chr3:37011153
|
C | T | 2 | a0001c0001t0001g0023a0004c0004t0001g0024 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.546-667C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37011153 | ||||||
| chr3:37011249
|
G | C | 1 | a0008c0009t0001g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.546-571G>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37011249 | ||||||
| chr3:37011383
|
G | A | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.546-437G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37011383 | ||||||
| chr3:37011442
|
G | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG01358.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.546-378G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37011442 | ||||||
| chr3:37011548
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.546-272G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37011548 | ||||||
| chr3:37011629
|
T | C | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.546-191T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37011629 | ||||||
| chr3:37011745
|
A | C | 9 | a0001c0001t0001g0257a0003c0003t0001g0015a0003c0003t0001g0212others(6): Show | 10 | HG00741.hp1 HG01109.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.546-75A>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37011745 | ||||||
| chr3:37011780
|
T | C | 2 | a0001c0001t0002g0064a0001c0001t0002g0065 | 2 | HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.546-40T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 6/18 | chr3 | 37011780 | ||||||
| chr3:37011873
|
G | C | 2 | a0001c0001t0001g0023a0004c0004t0001g0024 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.588+11G>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 7/18 | chr3 | 37011873 | ||||||
| chr3:37011986
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.589-25G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 7/18 | chr3 | 37011986 | ||||||
| chr3:37012267
|
C | A | 1 | a0001c0001t0001g0093 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.677+168C>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 8/18 | chr3 | 37012267 | ||||||
| chr3:37012316
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG02735.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.677+217G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 8/18 | chr3 | 37012316 | ||||||
| chr3:37012702
|
G | T | 1 | a0001c0001t0001g0097 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.677+603G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 8/18 | chr3 | 37012702 | ||||||
| chr3:37013110
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 109 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.677+1011T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 8/18 | chr3 | 37013110 | ||||||
| chr3:37013134
|
T | C | 7 | a0004c0004t0001g0187a0004c0004t0001g0188a0004c0004t0001g0197others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.677+1035T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 8/18 | chr3 | 37013134 | ||||||
| chr3:37013353
|
G | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG01255.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.678-1079G>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 8/18 | chr3 | 37013353 | ||||||
| chr3:37013506
|
C | T | 7 | a0001c0005t0001g0180a0001c0005t0001g0181a0001c0005t0001g0182others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.678-926C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 8/18 | chr3 | 37013506 | ||||||
| chr3:37013544
|
G | A | 2 | a0001c0001t0001g0023a0004c0004t0001g0024 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.678-888G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 8/18 | chr3 | 37013544 | ||||||
| chr3:37013670
|
T | C | 1 | a0002c0002t0001g0220 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.678-762T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 8/18 | chr3 | 37013670 | ||||||
| chr3:37013673
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.678-759C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 8/18 | chr3 | 37013673 | ||||||
| chr3:37013990
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG01255.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.678-442G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 8/18 | chr3 | 37013990 | ||||||
| chr3:37014195
|
G | GGTGA | 64 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(61): Show | 76 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.678-234_678-233ins others(4): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 37014195 | |||||
| chr3:37014216
|
A | G | 64 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(61): Show | 76 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.678-216A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 8/18 | chr3 | 37014216 | ||||||
| chr3:37014221
|
T | TGGATGGG others(1): Show |
64 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(61): Show | 76 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.678-203_678-196dup others(8): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 37014221 | |||||
| chr3:37014554
|
A | G | 1 | a0002c0002t0001g0235 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.790+10A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37014554 | ||||||
| chr3:37014740
|
GCTGGTTG others(11): Show |
G | 1 | a0001c0001t0001g0050 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.790+203_790+220del others(18): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 37014740 | |||||
| chr3:37015004
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.790+460A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37015004 | ||||||
| chr3:37015128
|
T | C | 1 | a0002c0002t0001g0231 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.790+584T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37015128 | ||||||
| chr3:37015415
|
G | T | 1 | a0001c0001t0001g0127 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.790+871G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37015415 | ||||||
| chr3:37015436
|
T | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02818.hp2 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.790+892T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37015436 | ||||||
| chr3:37015471
|
A | G | 2 | a0001c0001t0001g0023a0004c0004t0001g0024 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.790+927A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37015471 | ||||||
| chr3:37015499
|
C | A | 84 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(81): Show | 96 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.790+955C>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37015499 | ||||||
| chr3:37015819
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02735.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.790+1275G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37015819 | ||||||
| chr3:37015894
|
C | G | 2 | a0001c0001t0001g0023a0004c0004t0001g0024 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.790+1350C>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37015894 | ||||||
| chr3:37015960
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.790+1416G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37015960 | ||||||
| chr3:37016100
|
C | T | 65 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 77 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.791-1406C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37016100 | ||||||
| chr3:37016103
|
A | T | 1 | a0001c0005t0001g0185 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.791-1403A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37016103 | ||||||
| chr3:37016119
|
A | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0057a0001c0001t0001g0058others(7): Show | 11 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.791-1387A>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37016119 | ||||||
| chr3:37016171
|
G | A | 1 | a0001c0001t0002g0008 | 2 | HG01074.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.791-1335G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37016171 | ||||||
| chr3:37016184
|
T | A | 1 | a0003c0003t0001g0238 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.791-1322T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37016184 | ||||||
| chr3:37016201
|
C | T | 1 | a0002c0002t0001g0203 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.791-1305C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37016201 | ||||||
| chr3:37016225
|
G | T | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.791-1281G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37016225 | ||||||
| chr3:37016245
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.791-1261T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37016245 | ||||||
| chr3:37016520
|
C | A | 5 | a0001c0001t0002g0008a0001c0001t0002g0064a0001c0001t0002g0065others(2): Show | 6 | HG01074.hp2 HG01099.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.791-986C>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37016520 | ||||||
| chr3:37016791
|
C | A | 1 | a0001c0001t0002g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.791-715C>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37016791 | ||||||
| chr3:37016947
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.791-559C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37016947 | ||||||
| chr3:37017003
|
C | T | 7 | a0001c0005t0001g0180a0001c0005t0001g0181a0001c0005t0001g0182others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.791-503C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37017003 | ||||||
| chr3:37017018
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 109 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.791-488A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37017018 | ||||||
| chr3:37017284
|
T | G | 14 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0192others(11): Show | 14 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.791-222T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37017284 | ||||||
| chr3:37017443
|
G | A | 3 | a0001c0001t0001g0078a0001c0001t0001g0131a0001c0001t0001g0161 | 3 | HG01884.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.791-63G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 9/18 | chr3 | 37017443 | ||||||
| chr3:37017752
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.884+153A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37017752 | ||||||
| chr3:37018091
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0149a0001c0001t0001g0150 | 3 | HG00423.hp2 HG00544.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.884+492C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37018091 | ||||||
| chr3:37018124
|
A | G | 5 | a0001c0001t0002g0008a0001c0001t0002g0064a0001c0001t0002g0065others(2): Show | 6 | HG01074.hp2 HG01099.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.884+525A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37018124 | ||||||
| chr3:37018269
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.884+670T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37018269 | ||||||
| chr3:37018270
|
C | CA | 65 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 77 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.884+688dupA | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 37018270 | |||||
| chr3:37018293
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.884+694G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37018293 | ||||||
| chr3:37018392
|
A | T | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.884+793A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37018392 | ||||||
| chr3:37018444
|
G | A | 3 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | HG00280.hp1 HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.884+845G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37018444 | ||||||
| chr3:37018451
|
C | T | 14 | a0001c0001t0001g0025a0001c0001t0001g0033a0001c0001t0001g0034others(11): Show | 14 | HG00280.hp1 HG01346.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.884+852C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37018451 | ||||||
| chr3:37018761
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.884+1162G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37018761 | ||||||
| chr3:37018830
|
C | T | 65 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 77 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.884+1231C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37018830 | ||||||
| chr3:37018929
|
T | C | 7 | a0001c0005t0001g0180a0001c0005t0001g0181a0001c0005t0001g0182others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.884+1330T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37018929 | ||||||
| chr3:37018968
|
T | C | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.885-1342T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37018968 | ||||||
| chr3:37019078
|
G | T | 1 | a0001c0001t0002g0067 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.885-1232G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37019078 | ||||||
| chr3:37019159
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.885-1151C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37019159 | ||||||
| chr3:37019215
|
A | G | 3 | a0001c0001t0001g0189a0001c0001t0001g0191a0008c0009t0001g0190 | 3 | HG02717.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.885-1095A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37019215 | ||||||
| chr3:37019224
|
C | T | 7 | a0001c0005t0001g0180a0001c0005t0001g0181a0001c0005t0001g0182others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.885-1086C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37019224 | ||||||
| chr3:37019765
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.885-545G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37019765 | ||||||
| chr3:37019850
|
G | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0191a0008c0009t0001g0190 | 3 | HG02717.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.885-460G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37019850 | ||||||
| chr3:37019914
|
G | A | 7 | a0001c0005t0001g0180a0001c0005t0001g0181a0001c0005t0001g0182others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.885-396G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37019914 | ||||||
| chr3:37019969
|
C | T | 7 | a0001c0005t0001g0180a0001c0005t0001g0181a0001c0005t0001g0182others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.885-341C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37019969 | ||||||
| chr3:37020210
|
A | G | 1 | a0006c0007t0001g0176 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.885-100A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37020210 | ||||||
| chr3:37020229
|
G | C | 1 | a0001c0001t0002g0008 | 2 | HG01074.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.885-81G>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | chr3 | 37020229 | ||||||
| chr3:37020288
|
TTC | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.885-16_885-15delCT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 37020288 | |||||
| chr3:37020472
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1038+9G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37020472 | ||||||
| chr3:37020549
|
T | C | 84 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(81): Show | 96 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.1038+86T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37020549 | ||||||
| chr3:37020708
|
T | C | 7 | a0001c0005t0001g0180a0001c0005t0001g0181a0001c0005t0001g0182others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1038+245T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37020708 | ||||||
| chr3:37020709
|
A | T | 7 | a0004c0004t0001g0187a0004c0004t0001g0188a0004c0004t0001g0197others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1038+246A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37020709 | ||||||
| chr3:37020717
|
G | A | 12 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(9): Show | 12 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.1038+254G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37020717 | ||||||
| chr3:37020786
|
A | G | 10 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0005t0001g0180others(7): Show | 10 | HG02257.hp2 HG02280.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1038+323A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37020786 | ||||||
| chr3:37020790
|
C | A | 1 | a0001c0001t0001g0175 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1038+327C>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37020790 | ||||||
| chr3:37021024
|
T | G | 1 | a0001c0005t0001g0181 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1038+561T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37021024 | ||||||
| chr3:37021064
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1038+601A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37021064 | ||||||
| chr3:37021169
|
A | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG01255.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1038+706A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37021169 | ||||||
| chr3:37021351
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1038+888A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37021351 | ||||||
| chr3:37021363
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(74): Show | 89 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.1038+900C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37021363 | ||||||
| chr3:37021384
|
G | T | 1 | a0001c0001t0001g0040 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1038+921G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37021384 | ||||||
| chr3:37021438
|
G | C | 3 | a0001c0001t0001g0189a0001c0001t0001g0191a0008c0009t0001g0190 | 3 | HG02717.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1038+975G>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37021438 | ||||||
| chr3:37021468
|
G | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(74): Show | 89 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.1038+1005G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37021468 | ||||||
| chr3:37021757
|
A | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0132a0001c0001t0001g0175 | 3 | HG02615.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1038+1294A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37021757 | ||||||
| chr3:37021883
|
A | G | 3 | a0001c0001t0001g0189a0001c0001t0001g0191a0008c0009t0001g0190 | 3 | HG02717.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1038+1420A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37021883 | ||||||
| chr3:37022237
|
G | A | 65 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 77 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+1774G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37022237 | ||||||
| chr3:37022354
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1038+1891T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37022354 | ||||||
| chr3:37022416
|
T | C | 14 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(11): Show | 14 | HG00738.hp2 HG00741.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.1038+1953T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37022416 | ||||||
| chr3:37022419
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1038+1956A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37022419 | ||||||
| chr3:37022587
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1038+2124A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37022587 | ||||||
| chr3:37022916
|
C | T | 3 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0001g0233 | 5 | HG00544.hp2 NA18948.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.1038+2453C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37022916 | ||||||
| chr3:37023091
|
C | T | 5 | a0001c0001t0002g0008a0001c0001t0002g0064a0001c0001t0002g0065others(2): Show | 6 | HG01074.hp2 HG01099.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039-2546C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37023091 | ||||||
| chr3:37023220
|
C | A | 5 | a0001c0001t0002g0008a0001c0001t0002g0064a0001c0001t0002g0065others(2): Show | 6 | HG01074.hp2 HG01099.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039-2417C>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37023220 | ||||||
| chr3:37023281
|
A | G | 3 | a0001c0001t0001g0071a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG02895.hp1 HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1039-2356A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37023281 | ||||||
| chr3:37023391
|
C | A | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0215others(3): Show | 8 | NA18954.hp2 NA18964.hp1 NA18995.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039-2246C>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37023391 | ||||||
| chr3:37023646
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1039-1991G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37023646 | ||||||
| chr3:37023678
|
A | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0166 | 2 | HG01106.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1039-1959A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37023678 | ||||||
| chr3:37024114
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0068a0001c0001t0001g0089others(4): Show | 9 | HG00408.hp1 HG01496.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.1039-1523G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37024114 | ||||||
| chr3:37024178
|
A | T | 5 | a0001c0001t0002g0008a0001c0001t0002g0064a0001c0001t0002g0065others(2): Show | 6 | HG01074.hp2 HG01099.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039-1459A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37024178 | ||||||
| chr3:37024601
|
C | G | 1 | a0001c0001t0001g0170 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1039-1036C>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37024601 | ||||||
| chr3:37024770
|
A | G | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1039-867A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37024770 | ||||||
| chr3:37024790
|
TGTA | T | 7 | a0004c0004t0001g0187a0004c0004t0001g0188a0004c0004t0001g0197others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-844_1039-842d others(5): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr3 | 37024790 | |||||
| chr3:37024878
|
T | C | 83 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(80): Show | 95 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.1039-759T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37024878 | ||||||
| chr3:37024882
|
T | A | 98 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(95): Show | 111 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.1039-755T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37024882 | ||||||
| chr3:37025165
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1039-472A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37025165 | ||||||
| chr3:37025227
|
T | G | 1 | a0001c0001t0001g0046 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1039-410T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37025227 | ||||||
| chr3:37025301
|
T | C | 2 | a0001c0001t0001g0134a0001c0001t0001g0165 | 2 | HG02683.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1039-336T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37025301 | ||||||
| chr3:37025423
|
T | G | 1 | a0001c0001t0001g0047 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1039-214T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37025423 | ||||||
| chr3:37025559
|
A | G | 67 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 79 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1039-78A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37025559 | ||||||
| chr3:37025584
|
C | CTA | 6 | a0001c0001t0001g0083a0001c0001t0001g0137a0001c0001t0001g0138others(3): Show | 6 | HG01069.hp1 HG01123.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039-29_1039-28dup others(2): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr3 | 37025584 | |||||
| chr3:37025584
|
C | CTATA | 7 | a0001c0001t0001g0135a0004c0004t0001g0187a0004c0004t0001g0188others(4): Show | 7 | HG02129.hp1 HG02258.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-31_1039-28dup others(4): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr3 | 37025584 | |||||
| chr3:37025584
|
C | CTATATAT others(3): Show |
1 | a0001c0001t0001g0193 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1039-37_1039-28dup others(10): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr3 | 37025584 | |||||
| chr3:37025602
|
A | T | 12 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(9): Show | 12 | HG00738.hp2 HG00741.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.1039-35A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37025602 | ||||||
| chr3:37025602
|
ATATATAT others(1): Show |
A | 45 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(42): Show | 56 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1039-33_1039-26del others(8): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr3 | 37025602 | |||||
| chr3:37025603
|
TA | T | 6 | a0001c0001t0001g0058a0001c0001t0001g0116a0001c0001t0001g0163others(3): Show | 6 | HG01167.hp2 HG02145.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039-33delA | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37025603 | ||||||
| chr3:37025604
|
A | AT | 3 | a0001c0001t0001g0095a0001c0001t0001g0167a0005c0006t0001g0054 | 3 | HG02280.hp1 HG02647.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1039-32dupT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr3 | 37025604 | |||||
| chr3:37025604
|
A | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0029others(35): Show | 41 | HG00408.hp1 HG00639.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1039-33A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37025604 | ||||||
| chr3:37025604
|
ATATATTT | A | 7 | a0001c0001t0001g0210a0001c0001t0001g0217a0001c0001t0001g0247others(4): Show | 7 | HG01106.hp2 HG02559.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1039-31_1039-25del others(7): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr3 | 37025604 | |||||
| chr3:37025605
|
TA | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0069a0001c0001t0001g0074others(2): Show | 5 | HG03195.hp1 HG03195.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1039-31delA | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37025605 | ||||||
| chr3:37025606
|
A | AT | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0052others(3): Show | 6 | HG02735.hp2 HG03017.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039-30dupT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr3 | 37025606 | |||||
| chr3:37025606
|
A | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(76): Show | 87 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1039-31A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37025606 | ||||||
| chr3:37025606
|
ATATTTTT | A | 7 | a0003c0003t0001g0015a0003c0003t0001g0212a0003c0003t0001g0213others(4): Show | 8 | HG00741.hp1 HG01109.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1039-29_1039-23del others(7): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr3 | 37025606 | |||||
| chr3:37025608
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0195 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1039-28_1039-27ins others(13): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr3 | 37025608 | |||||
| chr3:37025608
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0196 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1039-28_1039-27ins others(14): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr3 | 37025608 | |||||
| chr3:37025608
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0192 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1039-28_1039-27ins others(12): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr3 | 37025608 | |||||
| chr3:37025608
|
A | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(109): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1039-29A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37025608 | ||||||
| chr3:37025610
|
T | A | 5 | a0001c0001t0001g0136a0004c0004t0001g0187a0004c0004t0001g0188others(2): Show | 5 | HG02258.hp1 HG03098.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1039-27T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37025610 | ||||||
| chr3:37025611
|
T | A | 1 | a0001c0001t0001g0194 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1039-26T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37025611 | ||||||
| chr3:37025629
|
T | A | 20 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0030others(17): Show | 21 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
splice_region_variant&intron_variant | LOW | c.1039-8T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | chr3 | 37025629 | ||||||
| chr3:37025629
|
T | TA | 4 | a0001c0001t0001g0039a0001c0001t0001g0044a0001c0001t0001g0057others(1): Show | 4 | HG00639.hp1 HG00738.hp2 HG02572.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1039-6dupA | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr3 | 37025629 | |||||
| chr3:37026118
|
C | G | 1 | a0001c0001t0001g0191 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1409+111C>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37026118 | ||||||
| chr3:37026149
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG01255.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1409+142C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37026149 | ||||||
| chr3:37026426
|
C | CT | 8 | a0001c0001t0001g0007a0001c0001t0001g0057a0001c0001t0001g0058others(5): Show | 9 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1409+425dupT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr3 | 37026426 | |||||
| chr3:37026498
|
C | T | 1 | a0003c0003t0001g0015 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1409+491C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37026498 | ||||||
| chr3:37026518
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1409+511G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37026518 | ||||||
| chr3:37026572
|
A | G | 3 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | HG00280.hp1 HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1409+565A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37026572 | ||||||
| chr3:37026588
|
T | C | 32 | a0001c0001t0001g0128a0001c0001t0001g0129a0002c0002t0001g0004others(29): Show | 36 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.1409+581T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37026588 | ||||||
| chr3:37026632
|
C | T | 2 | a0001c0001t0001g0023a0004c0004t0001g0024 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1409+625C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37026632 | ||||||
| chr3:37026650
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1409+643G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37026650 | ||||||
| chr3:37026706
|
G | A | 7 | a0001c0005t0001g0180a0001c0005t0001g0181a0001c0005t0001g0182others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1409+699G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37026706 | ||||||
| chr3:37026711
|
C | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1409+704C>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37026711 | ||||||
| chr3:37026713
|
C | T | 14 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(11): Show | 14 | HG00738.hp2 HG00741.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.1409+706C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37026713 | ||||||
| chr3:37026743
|
G | A | 1 | a0002c0002t0001g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1409+736G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37026743 | ||||||
| chr3:37026766
|
C | T | 67 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 79 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1409+759C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37026766 | ||||||
| chr3:37026840
|
GAAT | G | 15 | a0001c0001t0001g0023a0001c0001t0001g0094a0001c0001t0001g0192others(12): Show | 15 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.1409+860_1409+862d others(5): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr3 | 37026840 | |||||
| chr3:37026840
|
GAATAATA others(2): Show |
G | 67 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 79 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1409+854_1409+862d others(11): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr3 | 37026840 | |||||
| chr3:37026862
|
A | G | 2 | a0001c0001t0001g0023a0004c0004t0001g0024 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1409+855A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37026862 | ||||||
| chr3:37027066
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0140 | 2 | HG01243.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1409+1059G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37027066 | ||||||
| chr3:37027206
|
A | AAC | 15 | a0001c0001t0001g0032a0001c0001t0001g0046a0001c0001t0001g0099others(12): Show | 15 | HG02257.hp2 HG02280.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.1409+1226_1409+122 others(6): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr3 | 37027206 | |||||
| chr3:37027206
|
A | AACACAC | 5 | a0001c0001t0002g0008a0001c0001t0002g0064a0001c0001t0002g0065others(2): Show | 6 | HG01074.hp2 HG01099.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1409+1222_1409+122 others(10): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr3 | 37027206 | |||||
| chr3:37027206
|
AACAC | A | 83 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(80): Show | 95 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.1409+1224_1409+122 others(8): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr3 | 37027206 | |||||
| chr3:37027206
|
AACACACA others(3): Show |
A | 43 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0068others(40): Show | 45 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.1409+1218_1409+122 others(14): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr3 | 37027206 | |||||
| chr3:37027390
|
AAG | A | 12 | a0001c0001t0001g0023a0001c0001t0001g0193a0001c0001t0001g0194others(9): Show | 12 | HG01255.hp2 HG01934.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1409+1385_1409+138 others(6): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr3 | 37027390 | |||||
| chr3:37027478
|
G | A | 67 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 79 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1410-1306G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37027478 | ||||||
| chr3:37027547
|
G | C | 1 | a0003c0003t0001g0015 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1410-1237G>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37027547 | ||||||
| chr3:37028077
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1410-707G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37028077 | ||||||
| chr3:37028354
|
C | CA | 10 | a0001c0001t0001g0045a0001c0001t0001g0078a0001c0001t0001g0088others(7): Show | 10 | HG01884.hp1 HG02056.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1410-409dupA | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr3 | 37028354 | |||||
| chr3:37028354
|
CA | C | 18 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0111others(15): Show | 19 | HG00408.hp2 HG01069.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.1410-409delA | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr3 | 37028354 | |||||
| chr3:37028354
|
CAAA | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(78): Show | 93 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.1410-411_1410-409d others(5): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr3 | 37028354 | |||||
| chr3:37028381
|
T | G | 67 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 79 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1410-403T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37028381 | ||||||
| chr3:37028615
|
C | T | 67 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 79 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1410-169C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37028615 | ||||||
| chr3:37028717
|
C | G | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1410-67C>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37028717 | ||||||
| chr3:37028730
|
C | T | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1410-54C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 12/18 | chr3 | 37028730 | ||||||
| chr3:37028936
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02818.hp2 | splice_region_variant&intron_variant | LOW | c.1558+4C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37028936 | ||||||
| chr3:37028946
|
G | A | 24 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0030others(21): Show | 25 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.1558+14G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37028946 | ||||||
| chr3:37029264
|
A | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042 | 3 | HG00738.hp2 HG00741.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1558+332A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37029264 | ||||||
| chr3:37029572
|
C | T | 3 | a0001c0001t0001g0189a0001c0001t0001g0191a0008c0009t0001g0190 | 3 | HG02717.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1558+640C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37029572 | ||||||
| chr3:37029578
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1558+646C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37029578 | ||||||
| chr3:37029827
|
C | CT | 16 | a0001c0001t0001g0020a0001c0001t0001g0040a0001c0001t0001g0051others(13): Show | 17 | HG00544.hp1 HG00741.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.1558+914dupT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 37029827 | |||||
| chr3:37029827
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1558+895C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37029827 | ||||||
| chr3:37029827
|
CT | C | 8 | a0001c0001t0001g0042a0001c0001t0001g0094a0001c0001t0001g0114others(5): Show | 9 | HG01074.hp2 HG01099.hp2 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558+914delT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 37029827 | |||||
| chr3:37030408
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1558+1476G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37030408 | ||||||
| chr3:37030424
|
A | G | 14 | a0001c0001t0001g0025a0001c0001t0001g0033a0001c0001t0001g0034others(11): Show | 14 | HG00280.hp1 HG01346.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1558+1492A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37030424 | ||||||
| chr3:37030487
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1558+1555C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37030487 | ||||||
| chr3:37030495
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0057a0001c0001t0001g0058others(7): Show | 11 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.1558+1563C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37030495 | ||||||
| chr3:37030552
|
G | GA | 30 | a0001c0001t0001g0034a0001c0001t0001g0044a0001c0001t0001g0070others(27): Show | 31 | HG00738.hp1 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1558+1636dupA | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 37030552 | |||||
| chr3:37030552
|
G | GAA | 76 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(73): Show | 87 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.1558+1635_1558+163 others(6): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 37030552 | |||||
| chr3:37030552
|
G | GAAA | 6 | a0001c0001t0001g0207a0001c0001t0001g0210a0001c0001t0001g0216others(3): Show | 7 | HG00544.hp2 HG01192.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1558+1634_1558+163 others(7): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 37030552 | |||||
| chr3:37030614
|
A | G | 1 | a0001c0001t0001g0042 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1558+1682A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37030614 | ||||||
| chr3:37030727
|
G | A | 1 | a0007c0012t0001g0113 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1558+1795G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37030727 | ||||||
| chr3:37030973
|
T | C | 1 | a0007c0012t0001g0113 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1558+2041T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37030973 | ||||||
| chr3:37031136
|
A | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 79 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1558+2204A>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37031136 | ||||||
| chr3:37031214
|
G | A | 67 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 79 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1558+2282G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37031214 | ||||||
| chr3:37031437
|
G | T | 5 | a0001c0001t0002g0008a0001c0001t0002g0064a0001c0001t0002g0065others(2): Show | 6 | HG01074.hp2 HG01099.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1558+2505G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37031437 | ||||||
| chr3:37031438
|
A | T | 5 | a0001c0001t0002g0008a0001c0001t0002g0064a0001c0001t0002g0065others(2): Show | 6 | HG01074.hp2 HG01099.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1558+2506A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37031438 | ||||||
| chr3:37031448
|
G | A | 8 | a0003c0003t0001g0015a0003c0003t0001g0212a0003c0003t0001g0213others(5): Show | 9 | HG00741.hp1 HG01109.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558+2516G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37031448 | ||||||
| chr3:37031503
|
G | A | 1 | a0007c0012t0001g0113 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1558+2571G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37031503 | ||||||
| chr3:37031784
|
A | C | 7 | a0004c0004t0001g0187a0004c0004t0001g0188a0004c0004t0001g0197others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1558+2852A>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37031784 | ||||||
| chr3:37031796
|
T | G | 90 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(87): Show | 102 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.1558+2864T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37031796 | ||||||
| chr3:37032033
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1558+3101A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37032033 | ||||||
| chr3:37032088
|
T | G | 67 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 79 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1558+3156T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37032088 | ||||||
| chr3:37032174
|
G | C | 5 | a0001c0001t0002g0008a0001c0001t0002g0064a0001c0001t0002g0065others(2): Show | 6 | HG01074.hp2 HG01099.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1558+3242G>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37032174 | ||||||
| chr3:37032479
|
A | C | 1 | a0001c0001t0001g0195 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1558+3547A>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37032479 | ||||||
| chr3:37032481
|
C | G | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(1): Show | 4 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558+3549C>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37032481 | ||||||
| chr3:37032725
|
C | T | 1 | a0009c0011t0001g0073 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1558+3793C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37032725 | ||||||
| chr3:37032821
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1558+3889C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37032821 | ||||||
| chr3:37032829
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1558+3897C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37032829 | ||||||
| chr3:37032865
|
C | T | 4 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0001g0233others(1): Show | 6 | HG00544.hp2 NA18948.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558+3933C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37032865 | ||||||
| chr3:37032877
|
C | G | 67 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 79 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1558+3945C>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37032877 | ||||||
| chr3:37033033
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG01255.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1558+4101G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37033033 | ||||||
| chr3:37033160
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1558+4228C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37033160 | ||||||
| chr3:37033177
|
A | G | 14 | a0001c0001t0001g0025a0001c0001t0001g0033a0001c0001t0001g0034others(11): Show | 14 | HG00280.hp1 HG01346.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1558+4245A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37033177 | ||||||
| chr3:37033180
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1558+4248C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37033180 | ||||||
| chr3:37033185
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0003g0011a0001c0001t0003g0162 | 5 | HG02258.hp2 HG02622.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1558+4253G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37033185 | ||||||
| chr3:37033645
|
G | GTA | 4 | a0002c0002t0001g0222a0002c0002t0001g0224a0002c0002t0001g0225others(1): Show | 4 | HG01074.hp1 HG01099.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558+4717_1558+471 others(6): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 37033645 | |||||
| chr3:37033645
|
G | GTATA | 7 | a0004c0004t0001g0187a0004c0004t0001g0188a0004c0004t0001g0197others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1558+4715_1558+471 others(8): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 37033645 | |||||
| chr3:37033651
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 109 | HG00544.hp2 HG00639.hp2 HG00735.hp2 others(106): Show |
intron_variant | MODIFIER | c.1558+4719G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37033651 | ||||||
| chr3:37033987
|
C | T | 1 | a0004c0004t0001g0187 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1558+5055C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37033987 | ||||||
| chr3:37034068
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1558+5136C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37034068 | ||||||
| chr3:37034104
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1558+5172C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37034104 | ||||||
| chr3:37034132
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0057a0001c0001t0001g0058others(7): Show | 11 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.1558+5200G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37034132 | ||||||
| chr3:37034271
|
T | C | 3 | a0001c0001t0001g0095a0001c0001t0001g0106a0001c0001t0001g0115 | 3 | HG02109.hp2 HG02280.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1558+5339T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37034271 | ||||||
| chr3:37034443
|
T | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(95): Show | 111 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.1558+5511T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37034443 | ||||||
| chr3:37034446
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0149 | 2 | HG00597.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1558+5514G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37034446 | ||||||
| chr3:37034475
|
T | A | 1 | a0001c0001t0001g0121 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1558+5543T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37034475 | ||||||
| chr3:37034493
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0016others(122): Show | 139 | HG00099.hp1 HG00544.hp2 HG00639.hp1 others(136): Show |
intron_variant | MODIFIER | c.1558+5561A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37034493 | ||||||
| chr3:37034517
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1558+5585A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37034517 | ||||||
| chr3:37034968
|
G | T | 14 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0192others(11): Show | 14 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.1559-5218G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37034968 | ||||||
| chr3:37035136
|
G | A | 7 | a0004c0004t0001g0187a0004c0004t0001g0188a0004c0004t0001g0197others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1559-5050G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37035136 | ||||||
| chr3:37035253
|
T | G | 7 | a0001c0005t0001g0180a0001c0005t0001g0181a0001c0005t0001g0182others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1559-4933T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37035253 | ||||||
| chr3:37035338
|
C | A | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1559-4848C>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37035338 | ||||||
| chr3:37035536
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0124 | 2 | HG00423.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.1559-4650G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37035536 | ||||||
| chr3:37035578
|
T | G | 1 | a0001c0001t0001g0195 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1559-4608T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37035578 | ||||||
| chr3:37035808
|
G | A | 1 | a0002c0002t0001g0226 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1559-4378G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37035808 | ||||||
| chr3:37036019
|
C | CA | 15 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(12): Show | 15 | HG01255.hp2 HG01934.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1559-4155dupA | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 37036019 | |||||
| chr3:37036024
|
A | C | 11 | a0001c0001t0001g0007a0001c0001t0001g0057a0001c0001t0001g0058others(8): Show | 12 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1559-4162A>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37036024 | ||||||
| chr3:37036571
|
C | T | 7 | a0004c0004t0001g0187a0004c0004t0001g0188a0004c0004t0001g0197others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1559-3615C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37036571 | ||||||
| chr3:37036708
|
G | GT | 32 | a0001c0001t0001g0128a0001c0001t0001g0129a0002c0002t0001g0004others(29): Show | 36 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.1559-3476dupT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 37036708 | |||||
| chr3:37036763
|
A | G | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1559-3423A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37036763 | ||||||
| chr3:37036789
|
G | C | 83 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(80): Show | 95 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.1559-3397G>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37036789 | ||||||
| chr3:37036874
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042 | 3 | HG00738.hp2 HG00741.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1559-3312C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37036874 | ||||||
| chr3:37036988
|
C | T | 7 | a0001c0005t0001g0180a0001c0005t0001g0181a0001c0005t0001g0182others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1559-3198C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37036988 | ||||||
| chr3:37037001
|
C | T | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1559-3185C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37037001 | ||||||
| chr3:37037015
|
A | G | 67 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 79 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1559-3171A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37037015 | ||||||
| chr3:37037156
|
G | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0125a0001c0001t0001g0126others(1): Show | 4 | HG02602.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1559-3030G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37037156 | ||||||
| chr3:37037266
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1559-2920A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37037266 | ||||||
| chr3:37037487
|
T | A | 1 | a0008c0009t0001g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1559-2699T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37037487 | ||||||
| chr3:37037591
|
G | A | 2 | a0002c0002t0001g0227a0002c0002t0001g0230 | 2 | NA18956.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.1559-2595G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37037591 | ||||||
| chr3:37037593
|
C | T | 1 | a0002c0002t0001g0206 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1559-2593C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37037593 | ||||||
| chr3:37037681
|
G | A | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(1): Show | 4 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.1559-2505G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37037681 | ||||||
| chr3:37037862
|
G | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0191a0008c0009t0001g0190 | 3 | HG02717.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1559-2324G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37037862 | ||||||
| chr3:37038028
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1559-2158A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37038028 | ||||||
| chr3:37038141
|
G | C | 1 | a0001c0001t0001g0193 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1559-2045G>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37038141 | ||||||
| chr3:37038216
|
T | G | 1 | a0001c0001t0001g0257 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1559-1970T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37038216 | ||||||
| chr3:37038239
|
T | A | 1 | a0001c0001t0001g0179 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1559-1947T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37038239 | ||||||
| chr3:37038336
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02735.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1559-1850A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37038336 | ||||||
| chr3:37038895
|
G | T | 7 | a0001c0005t0001g0180a0001c0005t0001g0181a0001c0005t0001g0182others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1559-1291G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37038895 | ||||||
| chr3:37038942
|
A | G | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(1): Show | 4 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.1559-1244A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37038942 | ||||||
| chr3:37039001
|
G | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1559-1185G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37039001 | ||||||
| chr3:37039062
|
A | T | 1 | a0001c0001t0001g0146 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1559-1124A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37039062 | ||||||
| chr3:37039070
|
A | T | 14 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0192others(11): Show | 14 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.1559-1116A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37039070 | ||||||
| chr3:37039299
|
T | A | 1 | a0001c0001t0001g0078 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1559-887T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37039299 | ||||||
| chr3:37039304
|
A | G | 2 | a0001c0001t0001g0023a0004c0004t0001g0024 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1559-882A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37039304 | ||||||
| chr3:37039400
|
ATTTT | A | 14 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0192others(11): Show | 14 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.1559-781_1559-778d others(6): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 37039400 | |||||
| chr3:37039525
|
A | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0057a0001c0001t0001g0058others(7): Show | 11 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.1559-661A>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37039525 | ||||||
| chr3:37039578
|
A | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0153a0001c0001t0001g0155 | 3 | HG00140.hp2 HG01123.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1559-608A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37039578 | ||||||
| chr3:37039889
|
C | T | 3 | a0001c0001t0001g0099a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02818.hp2 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1559-297C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37039889 | ||||||
| chr3:37039895
|
T | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG01255.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1559-291T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37039895 | ||||||
| chr3:37039902
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1559-284T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 13/18 | chr3 | 37039902 | ||||||
| chr3:37040423
|
GTTTCAAA others(22): Show |
G | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1667+132_1667+160d others(31): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 37040423 | |||||
| chr3:37040541
|
T | TTTTG | 5 | a0001c0001t0001g0023a0001c0001t0001g0055a0001c0001t0001g0104others(2): Show | 5 | HG02523.hp1 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1667+273_1667+276d others(6): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 37040541 | |||||
| chr3:37040775
|
C | G | 1 | a0001c0001t0001g0258 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1667+481C>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37040775 | ||||||
| chr3:37040814
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1667+520A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37040814 | ||||||
| chr3:37040892
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1667+598A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37040892 | ||||||
| chr3:37041108
|
C | T | 14 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(11): Show | 14 | HG00738.hp2 HG00741.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.1667+814C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37041108 | ||||||
| chr3:37041122
|
A | G | 8 | a0003c0003t0001g0015a0003c0003t0001g0212a0003c0003t0001g0213others(5): Show | 9 | HG00741.hp1 HG01109.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1667+828A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37041122 | ||||||
| chr3:37041128
|
C | G | 1 | a0001c0001t0001g0257 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1667+834C>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37041128 | ||||||
| chr3:37041176
|
A | G | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1667+882A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37041176 | ||||||
| chr3:37041232
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1667+938A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37041232 | ||||||
| chr3:37041355
|
A | T | 1 | a0004c0004t0001g0024 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1668-913A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37041355 | ||||||
| chr3:37041383
|
T | C | 69 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(66): Show | 81 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.1668-885T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37041383 | ||||||
| chr3:37041388
|
A | G | 1 | a0002c0002t0001g0221 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1668-880A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37041388 | ||||||
| chr3:37041417
|
C | T | 14 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(11): Show | 14 | HG00738.hp2 HG00741.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.1668-851C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37041417 | ||||||
| chr3:37041517
|
T | C | 1 | a0004c0004t0001g0024 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1668-751T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37041517 | ||||||
| chr3:37041610
|
C | G | 1 | a0001c0001t0001g0095 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1668-658C>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37041610 | ||||||
| chr3:37041852
|
T | C | 8 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0002g0008others(5): Show | 9 | HG01074.hp2 HG01099.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1668-416T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37041852 | ||||||
| chr3:37041916
|
G | GA | 90 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(87): Show | 102 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.1668-350dupA | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 37041916 | |||||
| chr3:37041949
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1668-319C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37041949 | ||||||
| chr3:37042014
|
C | T | 2 | a0001c0001t0001g0139a0001c0001t0001g0144 | 2 | HG01069.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1668-254C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37042014 | ||||||
| chr3:37042083
|
T | C | 23 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(20): Show | 23 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.1668-185T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37042083 | ||||||
| chr3:37042159
|
T | G | 1 | a0002c0002t0001g0231 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1668-109T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37042159 | ||||||
| chr3:37042172
|
A | G | 1 | a0001c0001t0002g0065 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1668-96A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37042172 | ||||||
| chr3:37042249
|
A | G | 90 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(87): Show | 102 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.1668-19A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 14/18 | chr3 | 37042249 | ||||||
| chr3:37042556
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1731+225G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37042556 | ||||||
| chr3:37042578
|
C | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0057a0001c0001t0001g0058others(5): Show | 9 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1731+247C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37042578 | ||||||
| chr3:37042816
|
C | T | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1731+485C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37042816 | ||||||
| chr3:37042817
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02735.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1731+486G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37042817 | ||||||
| chr3:37043241
|
C | A | 2 | a0001c0001t0001g0023a0004c0004t0001g0024 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1731+910C>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37043241 | ||||||
| chr3:37043254
|
A | C | 8 | a0003c0003t0001g0015a0003c0003t0001g0212a0003c0003t0001g0213others(5): Show | 9 | HG00741.hp1 HG01109.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1731+923A>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37043254 | ||||||
| chr3:37043512
|
G | A | 5 | a0003c0003t0001g0212a0003c0003t0001g0213a0003c0003t0001g0214others(2): Show | 5 | HG00741.hp1 HG01109.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1731+1181G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37043512 | ||||||
| chr3:37043546
|
AT | A | 13 | a0001c0001t0001g0023a0001c0001t0001g0069a0001c0001t0001g0074others(10): Show | 13 | HG00099.hp1 HG01934.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1731+1235delT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 37043546 | |||||
| chr3:37043615
|
T | A | 1 | a0002c0002t0001g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1731+1284T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37043615 | ||||||
| chr3:37043697
|
T | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0068a0001c0001t0001g0089others(4): Show | 9 | HG00408.hp1 HG01496.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.1731+1366T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37043697 | ||||||
| chr3:37043795
|
G | A | 5 | a0001c0001t0001g0093a0001c0001t0001g0107a0001c0001t0001g0108others(2): Show | 5 | HG01243.hp2 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1731+1464G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37043795 | ||||||
| chr3:37043823
|
C | G | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1731+1492C>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37043823 | ||||||
| chr3:37043853
|
T | G | 3 | a0001c0001t0002g0008a0001c0001t0002g0064a0001c0001t0002g0065 | 4 | HG01074.hp2 HG01099.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1731+1522T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37043853 | ||||||
| chr3:37044333
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1731+2002C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37044333 | ||||||
| chr3:37044334
|
G | A | 2 | a0002c0002t0001g0234a0002c0002t0001g0235 | 2 | HG00099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1731+2003G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37044334 | ||||||
| chr3:37044349
|
A | C | 24 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0030others(21): Show | 25 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.1731+2018A>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37044349 | ||||||
| chr3:37044373
|
C | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0155 | 2 | HG00140.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1731+2042C>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37044373 | ||||||
| chr3:37044373
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0251 | 3 | HG03490.hp2 HG03492.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1731+2042C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37044373 | ||||||
| chr3:37044448
|
C | T | 4 | a0001c0001t0001g0025a0001c0001t0001g0070a0001c0001t0001g0101others(1): Show | 4 | HG02056.hp1 NA19000.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1731+2117C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37044448 | ||||||
| chr3:37044479
|
T | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 79 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1731+2148T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37044479 | ||||||
| chr3:37044512
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1731+2181C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37044512 | ||||||
| chr3:37044526
|
C | G | 7 | a0001c0005t0001g0180a0001c0005t0001g0181a0001c0005t0001g0182others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1731+2195C>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37044526 | ||||||
| chr3:37044528
|
C | CTT | 8 | a0003c0003t0001g0015a0003c0003t0001g0212a0003c0003t0001g0213others(5): Show | 9 | HG00741.hp1 HG01109.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1731+2198_1731+219 others(6): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 37044528 | |||||
| chr3:37044713
|
G | A | 83 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(80): Show | 95 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.1731+2382G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37044713 | ||||||
| chr3:37044763
|
C | T | 1 | a0009c0011t0001g0073 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1731+2432C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37044763 | ||||||
| chr3:37044773
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1731+2442A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37044773 | ||||||
| chr3:37044825
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1731+2494G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37044825 | ||||||
| chr3:37044844
|
T | C | 2 | a0001c0001t0001g0023a0004c0004t0001g0024 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1731+2513T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37044844 | ||||||
| chr3:37044920
|
A | G | 1 | a0008c0009t0001g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1731+2589A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37044920 | ||||||
| chr3:37044925
|
A | G | 1 | a0002c0002t0001g0202 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1731+2594A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37044925 | ||||||
| chr3:37044973
|
A | C | 12 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(9): Show | 12 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.1732-2546A>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37044973 | ||||||
| chr3:37045089
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1732-2430T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37045089 | ||||||
| chr3:37045146
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0155 | 2 | HG00140.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1732-2373G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37045146 | ||||||
| chr3:37045197
|
T | C | 8 | a0003c0003t0001g0015a0003c0003t0001g0212a0003c0003t0001g0213others(5): Show | 9 | HG00741.hp1 HG01109.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1732-2322T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37045197 | ||||||
| chr3:37045214
|
G | T | 2 | a0001c0001t0001g0023a0004c0004t0001g0024 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1732-2305G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37045214 | ||||||
| chr3:37045431
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1732-2088C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37045431 | ||||||
| chr3:37045459
|
T | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0175 | 2 | HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1732-2060T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37045459 | ||||||
| chr3:37045642
|
C | G | 14 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(11): Show | 14 | HG00738.hp2 HG00741.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.1732-1877C>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37045642 | ||||||
| chr3:37045688
|
T | C | 1 | a0002c0002t0001g0202 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1732-1831T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37045688 | ||||||
| chr3:37045702
|
C | CT | 36 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(33): Show | 39 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.1732-1792dupT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 37045702 | |||||
| chr3:37045702
|
CT | C | 29 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(26): Show | 31 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1732-1792delT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 37045702 | |||||
| chr3:37045704
|
T | C | 1 | a0008c0009t0001g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1732-1815T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37045704 | ||||||
| chr3:37045926
|
C | T | 67 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 79 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1732-1593C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37045926 | ||||||
| chr3:37045939
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1732-1580C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37045939 | ||||||
| chr3:37045989
|
G | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1530G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37045989 | ||||||
| chr3:37045991
|
G | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1528G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37045991 | ||||||
| chr3:37045992
|
A | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1527A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37045992 | ||||||
| chr3:37045993
|
G | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1526G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37045993 | ||||||
| chr3:37045994
|
C | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1525C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37045994 | ||||||
| chr3:37045995
|
C | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1524C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37045995 | ||||||
| chr3:37045996
|
A | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1523A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37045996 | ||||||
| chr3:37045997
|
C | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1522C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37045997 | ||||||
| chr3:37045999
|
G | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1520G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37045999 | ||||||
| chr3:37046001
|
G | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1518G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046001 | ||||||
| chr3:37046002
|
G | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1517G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046002 | ||||||
| chr3:37046003
|
C | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1516C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046003 | ||||||
| chr3:37046005
|
G | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1514G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046005 | ||||||
| chr3:37046006
|
G | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1513G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046006 | ||||||
| chr3:37046007
|
C | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1512C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046007 | ||||||
| chr3:37046008
|
C | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1511C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046008 | ||||||
| chr3:37046010
|
G | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1509G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046010 | ||||||
| chr3:37046014
|
C | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1505C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046014 | ||||||
| chr3:37046015
|
A | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1504A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046015 | ||||||
| chr3:37046016
|
C | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1503C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046016 | ||||||
| chr3:37046017
|
A | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1502A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046017 | ||||||
| chr3:37046021
|
C | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1498C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046021 | ||||||
| chr3:37046024
|
A | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1495A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046024 | ||||||
| chr3:37046025
|
A | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1494A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046025 | ||||||
| chr3:37046026
|
G | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1493G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046026 | ||||||
| chr3:37046027
|
G | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1492G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046027 | ||||||
| chr3:37046029
|
A | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1490A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046029 | ||||||
| chr3:37046030
|
G | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1489G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046030 | ||||||
| chr3:37046031
|
A | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1488A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046031 | ||||||
| chr3:37046032
|
A | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1487A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046032 | ||||||
| chr3:37046033
|
G | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1486G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046033 | ||||||
| chr3:37046034
|
C | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1485C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046034 | ||||||
| chr3:37046036
|
G | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1483G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046036 | ||||||
| chr3:37046037
|
A | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1482A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046037 | ||||||
| chr3:37046038
|
G | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1481G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046038 | ||||||
| chr3:37046039
|
G | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1480G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046039 | ||||||
| chr3:37046041
|
C | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1478C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046041 | ||||||
| chr3:37046042
|
A | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1477A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046042 | ||||||
| chr3:37046043
|
C | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1476C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046043 | ||||||
| chr3:37046044
|
G | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1475G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046044 | ||||||
| chr3:37046045
|
G | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1474G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046045 | ||||||
| chr3:37046046
|
A | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1473A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046046 | ||||||
| chr3:37046050
|
G | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1469G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046050 | ||||||
| chr3:37046051
|
A | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1468A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046051 | ||||||
| chr3:37046052
|
G | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1467G>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046052 | ||||||
| chr3:37046053
|
A | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1466A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046053 | ||||||
| chr3:37046054
|
C | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1465C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046054 | ||||||
| chr3:37046055
|
C | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1464C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046055 | ||||||
| chr3:37046059
|
C | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1460C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046059 | ||||||
| chr3:37046062
|
C | T | 1 | a0002c0002t0001g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1732-1457C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046062 | ||||||
| chr3:37046260
|
A | G | 2 | a0002c0002t0001g0227a0002c0002t0001g0230 | 2 | NA18956.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.1732-1259A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046260 | ||||||
| chr3:37046335
|
CT | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0132a0001c0001t0001g0175 | 3 | HG02615.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1732-1177delT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 37046335 | |||||
| chr3:37046597
|
G | GTA | 14 | a0001c0001t0001g0007a0001c0001t0001g0057a0001c0001t0001g0058others(11): Show | 15 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1732-908_1732-907d others(4): Show |
MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 37046597 | |||||
| chr3:37046605
|
A | AT | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0257 | 3 | HG02735.hp2 HG02818.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1732-913dupT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 37046605 | |||||
| chr3:37046606
|
TA | T | 17 | a0001c0001t0001g0023a0001c0001t0001g0192a0001c0001t0001g0193others(14): Show | 17 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.1732-912delA | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046606 | ||||||
| chr3:37046607
|
A | T | 62 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(59): Show | 74 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1732-912A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046607 | ||||||
| chr3:37046608
|
T | A | 62 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(59): Show | 74 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1732-911T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046608 | ||||||
| chr3:37046609
|
A | AT | 9 | a0001c0001t0001g0256a0001c0005t0001g0180a0001c0005t0001g0181others(6): Show | 9 | HG02145.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1732-909dupT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 37046609 | |||||
| chr3:37046609
|
A | T | 83 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(80): Show | 95 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.1732-910A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046609 | ||||||
| chr3:37046610
|
TA | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0096a0001c0001t0001g0132others(2): Show | 5 | HG00099.hp2 HG02922.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1732-908delA | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046610 | ||||||
| chr3:37046611
|
A | AT | 26 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0025others(23): Show | 29 | HG00280.hp1 HG01074.hp2 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.1732-895dupT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 37046611 | |||||
| chr3:37046611
|
A | T | 133 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0016others(130): Show | 147 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(144): Show |
intron_variant | MODIFIER | c.1732-908A>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046611 | ||||||
| chr3:37046613
|
T | A | 4 | a0001c0001t0001g0063a0001c0001t0001g0080a0001c0001t0001g0135others(1): Show | 4 | HG00639.hp1 HG02129.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1732-906T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046613 | ||||||
| chr3:37046711
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1732-808A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37046711 | ||||||
| chr3:37047367
|
G | C | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(1): Show | 4 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.1732-152G>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37047367 | ||||||
| chr3:37047500
|
T | A | 2 | a0001c0001t0001g0023a0004c0004t0001g0024 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1732-19T>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 15/18 | chr3 | 37047500 | ||||||
| chr3:37047966
|
G | A | 1 | a0002c0002t0001g0224 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1896+283G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 16/18 | chr3 | 37047966 | ||||||
| chr3:37048007
|
T | C | 1 | a0001c0001t0002g0066 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1896+324T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 16/18 | chr3 | 37048007 | ||||||
| chr3:37048014
|
CA | C | 97 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(94): Show | 110 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.1896+346delA | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr3 | 37048014 | |||||
| chr3:37048093
|
C | T | 14 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0192others(11): Show | 14 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.1896+410C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 16/18 | chr3 | 37048093 | ||||||
| chr3:37048158
|
T | C | 15 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0002g0008others(12): Show | 16 | HG01074.hp2 HG01099.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1897-359T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 16/18 | chr3 | 37048158 | ||||||
| chr3:37048220
|
T | C | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1897-297T>C | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 16/18 | chr3 | 37048220 | ||||||
| chr3:37048315
|
T | G | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1897-202T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 16/18 | chr3 | 37048315 | ||||||
| chr3:37048349
|
CT | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(95): Show | 111 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.1897-162delT | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr3 | 37048349 | |||||
| chr3:37048372
|
C | G | 1 | a0001c0001t0001g0074 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1897-145C>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 16/18 | chr3 | 37048372 | ||||||
| chr3:37048783
|
C | T | 83 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(80): Show | 95 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.1990-121C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 17/18 | chr3 | 37048783 | ||||||
| chr3:37048898
|
G | A | 4 | a0002c0002t0001g0209a0002c0002t0001g0223a0002c0002t0001g0228others(1): Show | 4 | NA18966.hp2 NA18967.hp2 NA19006.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1990-6G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 17/18 | chr3 | 37048898 | ||||||
| chr3:37049249
|
G | A | 4 | a0002c0002t0001g0209a0002c0002t0001g0223a0002c0002t0001g0228others(1): Show | 4 | NA18966.hp2 NA18967.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.2103+232G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 18/18 | chr3 | 37049249 | ||||||
| chr3:37049401
|
C | A | 1 | a0002c0002t0001g0230 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2103+384C>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 18/18 | chr3 | 37049401 | ||||||
| chr3:37049402
|
A | G | 1 | a0002c0002t0001g0230 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2103+385A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 18/18 | chr3 | 37049402 | ||||||
| chr3:37049404
|
G | A | 1 | a0002c0002t0001g0230 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2103+387G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 18/18 | chr3 | 37049404 | ||||||
| chr3:37049464
|
T | G | 7 | a0001c0005t0001g0180a0001c0005t0001g0181a0001c0005t0001g0182others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2103+447T>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 18/18 | chr3 | 37049464 | ||||||
| chr3:37049834
|
G | A | 67 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 79 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.2104-652G>A | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 18/18 | chr3 | 37049834 | ||||||
| chr3:37049863
|
A | G | 12 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(9): Show | 12 | HG01255.hp2 HG01884.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.2104-623A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 18/18 | chr3 | 37049863 | ||||||
| chr3:37050190
|
C | T | 1 | a0001c0005t0001g0184 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2104-296C>T | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 18/18 | chr3 | 37050190 | ||||||
| chr3:37050203
|
A | G | 11 | a0001c0001t0001g0025a0001c0001t0001g0033a0001c0001t0001g0034others(8): Show | 11 | HG00280.hp1 HG01346.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.2104-283A>G | MLH1 | ENSG00000076242.17 | transcript | ENST00000231790.8 | protein_coding | 18/18 | chr3 | 37050203 |