Search by Gene
| geneid | 130752 |
|---|---|
| ensemblid | ENSG00000138400.13 |
| hgncid | 17836 |
| symbol | MDH1B |
| name | malate dehydrogenase 1B |
| refseq_nuc | NM_001039845.3 |
| refseq_prot | NP_001034934.1 |
| ensembl_nuc | ENST00000374412.8 |
| ensembl_prot | ENSP00000363533.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 206737763 |
| end | 206765328 |
| strand | - |
| ver | v1.2 |
| region | chr2:206737763-206765328 |
| region5000 | chr2:206732763-206770328 |
| regionname0 | MDH1B_chr2_206737763_206765328 |
| regionname5000 | MDH1B_chr2_206732763_206770328 |
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 | 518 | 224 | 51 | 47 | 85 | 10 | 29 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0002 | 0/0 | 518 | 98 | 29 | 11 | 52 | 1 | 5 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0003 | 0/0 | 518 | 23 | 1 | 2 | 18 | 0 | 2 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0004 | 0/0 | 518 | 17 | 9 | 1 | 1 | 1 | 5 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0005 | 0/0 | 518 | 3 | 2 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0006 | 0/0 | 518 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0007 | 0/0 | 518 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0008 | 0/0 | 518 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0009 | 0/0 | 518 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | 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 | 1557 | 188 | 39 | 46 | 69 | 10 | 22 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| c0002 | 0/0 | 1557 | 88 | 20 | 11 | 51 | 1 | 5 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| c0003 | 0/0 | 1557 | 34 | 12 | 1 | 16 | 0 | 5 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| c0004 | 0/0 | 1557 | 23 | 1 | 2 | 18 | 0 | 2 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| c0005 | 0/0 | 1557 | 11 | 9 | 0 | 1 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| c0006 | 0/0 | 1557 | 9 | 9 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| c0007 | 0/0 | 1557 | 6 | 0 | 1 | 0 | 1 | 4 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| c0008 | 0/0 | 1557 | 3 | 2 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| c0009 | 0/0 | 1557 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| c0010 | 0/0 | 1557 | 2 | 0 | 0 | 0 | 0 | 2 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| c0011 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| c0012 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| c0013 | 0/0 | 1557 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| c0014 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | 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 | 778 | 258 | 84 | 48 | 84 | 10 | 30 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| t0002 | 0/0 | 778 | 107 | 10 | 14 | 69 | 2 | 12 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| t0003 | 0/0 | 774 | 4 | 0 | 0 | 4 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| t0004 | 0/0 | 778 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | 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 | 41 | 6 | 6 | 23 | 3 | 3 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0002 | 0/0 | 23 | 0 | 2 | 15 | 1 | 5 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0003 | 0/0 | 14 | 0 | 4 | 9 | 1 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0004 | 0/0 | 13 | 0 | 9 | 2 | 0 | 2 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0005 | 0/0 | 12 | 0 | 4 | 8 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0006 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0007 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0008 | 1/0 | 7 | 3 | 1 | 0 | 1 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0009 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0010 | 0/0 | 6 | 0 | 0 | 2 | 0 | 4 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0011 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0013 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0021 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0022 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0038 | 0/1 | 2 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| 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 | 188 | 39 | 46 | 69 | 10 | 22 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 34 | 12 | 1 | 16 | 0 | 5 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0001c0010 | a0001 | c0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0002c0002 | a0002 | c0002 | 0/0 | 88 | 20 | 11 | 51 | 1 | 5 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0002c0006 | a0002 | c0006 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0002c0011 | a0002 | c0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0003c0004 | a0003 | c0004 | 0/0 | 23 | 1 | 2 | 18 | 0 | 2 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0004c0005 | a0004 | c0005 | 0/0 | 11 | 9 | 0 | 1 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0004c0007 | a0004 | c0007 | 0/0 | 6 | 0 | 1 | 0 | 1 | 4 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0005c0008 | a0005 | c0008 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0006c0009 | a0006 | c0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0007c0012 | a0007 | c0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0008c0013 | a0008 | c0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0009c0014 | a0009 | c0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | 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 | 188 | 39 | 46 | 69 | 10 | 22 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0001c0003t0001 | a0001 | c0003 | t0001 | 0/0 | 33 | 12 | 1 | 15 | 0 | 5 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0001c0003t0004 | a0001 | c0003 | t0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0001c0010t0001 | a0001 | c0010 | t0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0002c0002t0001 | a0002 | c0002 | t0001 | 0/0 | 21 | 20 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0002c0002t0002 | a0002 | c0002 | t0002 | 0/0 | 67 | 0 | 10 | 51 | 1 | 5 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0002c0006t0001 | a0002 | c0006 | t0001 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0002c0011t0002 | a0002 | c0011 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0003c0004t0002 | a0003 | c0004 | t0002 | 0/0 | 19 | 1 | 2 | 14 | 0 | 2 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0003c0004t0003 | a0003 | c0004 | t0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0004c0005t0001 | a0004 | c0005 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0004c0005t0002 | a0004 | c0005 | t0002 | 0/0 | 10 | 8 | 0 | 1 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0004c0007t0002 | a0004 | c0007 | t0002 | 0/0 | 6 | 0 | 1 | 0 | 1 | 4 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0005c0008t0001 | a0005 | c0008 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0005c0008t0002 | a0005 | c0008 | t0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0006c0009t0002 | a0006 | c0009 | t0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0007c0012t0001 | a0007 | c0012 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0008c0013t0001 | a0008 | c0013 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B | copy fasta |
| a0009c0014t0001 | a0009 | c0014 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B | 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 | 41 | 6 | 6 | 23 | 3 | 3 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 23 | 0 | 2 | 15 | 1 | 5 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 13 | 0 | 9 | 2 | 0 | 2 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 1/0 | 7 | 3 | 1 | 0 | 1 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0011 | a0001 | c0001 | t0001 | g0011 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0018 | a0001 | c0001 | t0001 | g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/1 | 2 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0174 | a0001 | c0001 | t0001 | g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0176 | a0001 | c0001 | t0001 | g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0003t0001g0006 | a0001 | c0003 | t0001 | g0006 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0003t0001g0010 | a0001 | c0003 | t0001 | g0010 | 0/0 | 6 | 0 | 0 | 2 | 0 | 4 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0003t0001g0023 | a0001 | c0003 | t0001 | g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0003t0001g0024 | a0001 | c0003 | t0001 | g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0003t0001g0048 | a0001 | c0003 | t0001 | g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0003t0001g0154 | a0001 | c0003 | t0001 | g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0003t0001g0156 | a0001 | c0003 | t0001 | g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0003t0001g0157 | a0001 | c0003 | t0001 | g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0003t0001g0161 | a0001 | c0003 | t0001 | g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0003t0001g0162 | a0001 | c0003 | t0001 | g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0003t0001g0163 | a0001 | c0003 | t0001 | g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0003t0001g0165 | a0001 | c0003 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0003t0001g0166 | a0001 | c0003 | t0001 | g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0003t0001g0171 | a0001 | c0003 | t0001 | g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0003t0004g0164 | a0001 | c0003 | t0004 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0010t0001g0082 | a0001 | c0010 | t0001 | g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0001c0010t0001g0083 | a0001 | c0010 | t0001 | g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0001g0016 | a0002 | c0002 | t0001 | g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0001g0017 | a0002 | c0002 | t0001 | g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0001g0019 | a0002 | c0002 | t0001 | g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0001g0079 | a0002 | c0002 | t0001 | g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0001g0085 | a0002 | c0002 | t0001 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0001g0092 | a0002 | c0002 | t0001 | g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0001g0093 | a0002 | c0002 | t0001 | g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0001g0141 | a0002 | c0002 | t0001 | g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0001g0152 | a0002 | c0002 | t0001 | g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0001g0172 | a0002 | c0002 | t0001 | g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0001g0173 | a0002 | c0002 | t0001 | g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0001g0175 | a0002 | c0002 | t0001 | g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0001g0178 | a0002 | c0002 | t0001 | g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0003 | a0002 | c0002 | t0002 | g0003 | 0/0 | 14 | 0 | 4 | 9 | 1 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0005 | a0002 | c0002 | t0002 | g0005 | 0/0 | 12 | 0 | 4 | 8 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0009 | a0002 | c0002 | t0002 | g0009 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0037 | a0002 | c0002 | t0002 | g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0039 | a0002 | c0002 | t0002 | g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0040 | a0002 | c0002 | t0002 | g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0102 | a0002 | c0002 | t0002 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0104 | a0002 | c0002 | t0002 | g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0105 | a0002 | c0002 | t0002 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0106 | a0002 | c0002 | t0002 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0107 | a0002 | c0002 | t0002 | g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0108 | a0002 | c0002 | t0002 | g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0109 | a0002 | c0002 | t0002 | g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0111 | a0002 | c0002 | t0002 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0113 | a0002 | c0002 | t0002 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0115 | a0002 | c0002 | t0002 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0117 | a0002 | c0002 | t0002 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0118 | a0002 | c0002 | t0002 | g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0119 | a0002 | c0002 | t0002 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0127 | a0002 | c0002 | t0002 | g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0130 | a0002 | c0002 | t0002 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0131 | a0002 | c0002 | t0002 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0132 | a0002 | c0002 | t0002 | g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0133 | a0002 | c0002 | t0002 | g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0134 | a0002 | c0002 | t0002 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0135 | a0002 | c0002 | t0002 | g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0136 | a0002 | c0002 | t0002 | g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0138 | a0002 | c0002 | t0002 | g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0140 | a0002 | c0002 | t0002 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0143 | a0002 | c0002 | t0002 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0144 | a0002 | c0002 | t0002 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0145 | a0002 | c0002 | t0002 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0147 | a0002 | c0002 | t0002 | g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0002t0002g0149 | a0002 | c0002 | t0002 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0006t0001g0044 | a0002 | c0006 | t0001 | g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0006t0001g0047 | a0002 | c0006 | t0001 | g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0006t0001g0153 | a0002 | c0006 | t0001 | g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0006t0001g0158 | a0002 | c0006 | t0001 | g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0006t0001g0159 | a0002 | c0006 | t0001 | g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0006t0001g0160 | a0002 | c0006 | t0001 | g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0006t0001g0168 | a0002 | c0006 | t0001 | g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0002c0011t0002g0146 | a0002 | c0011 | t0002 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0003c0004t0002g0007 | a0003 | c0004 | t0002 | g0007 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0003c0004t0002g0020 | a0003 | c0004 | t0002 | g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0003c0004t0002g0027 | a0003 | c0004 | t0002 | g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0003c0004t0002g0055 | a0003 | c0004 | t0002 | g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0003c0004t0002g0056 | a0003 | c0004 | t0002 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0003c0004t0002g0058 | a0003 | c0004 | t0002 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0003c0004t0002g0086 | a0003 | c0004 | t0002 | g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0003c0004t0002g0088 | a0003 | c0004 | t0002 | g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0003c0004t0002g0095 | a0003 | c0004 | t0002 | g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0003c0004t0003g0026 | a0003 | c0004 | t0003 | g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0003c0004t0003g0057 | a0003 | c0004 | t0003 | g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0003c0004t0003g0059 | a0003 | c0004 | t0003 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0004c0005t0001g0125 | a0004 | c0005 | t0001 | g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0004c0005t0002g0015 | a0004 | c0005 | t0002 | g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0004c0005t0002g0042 | a0004 | c0005 | t0002 | g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0004c0005t0002g0078 | a0004 | c0005 | t0002 | g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0004c0005t0002g0110 | a0004 | c0005 | t0002 | g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0004c0005t0002g0114 | a0004 | c0005 | t0002 | g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0004c0005t0002g0124 | a0004 | c0005 | t0002 | g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0004c0007t0002g0045 | a0004 | c0007 | t0002 | g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0004c0007t0002g0046 | a0004 | c0007 | t0002 | g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0004c0007t0002g0155 | a0004 | c0007 | t0002 | g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0004c0007t0002g0167 | a0004 | c0007 | t0002 | g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0005c0008t0001g0061 | a0005 | c0008 | t0001 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0005c0008t0002g0051 | a0005 | c0008 | t0002 | g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0005c0008t0002g0060 | a0005 | c0008 | t0002 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0006c0009t0002g0029 | a0006 | c0009 | t0002 | g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0007c0012t0001g0077 | a0007 | c0012 | t0001 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0008c0013t0001g0080 | a0008 | c0013 | t0001 | g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH1B_chr2_206732763_206770328 | MDH1B |
| a0009c0014t0001g0151 | a0009 | c0014 | t0001 | g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH1B_chr2_206732763_206770328 | MDH1B |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | GBR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00280 | hp2 | a0004 | c0007 | t0002 | g0045 | EUR | FIN | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0003 | EUR | FIN | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | CHS | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | CHS | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00423 | hp2 | a0001 | c0003 | t0001 | g0010 | EAS | CHS | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | CHS | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0130 | EAS | CHS | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0119 | EAS | CHS | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00642 | hp2 | a0004 | c0007 | t0002 | g0045 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | CHS | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01109 | hp1 | a0005 | c0008 | t0002 | g0051 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01175 | hp1 | a0003 | c0004 | t0002 | g0007 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0132 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0171 | AMR | CLM | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01261 | hp1 | a0003 | c0004 | t0002 | g0027 | AMR | CLM | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0135 | EAS | KHV | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0133 | EAS | KHV | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02027 | hp2 | a0001 | c0003 | t0001 | g0010 | EAS | KHV | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0085 | AFR | ACB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0156 | AFR | ACB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02056 | hp2 | a0001 | c0003 | t0004 | g0164 | EAS | KHV | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0145 | EAS | KHV | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02129 | hp1 | a0003 | c0004 | t0002 | g0020 | EAS | KHV | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02135 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | KHV | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02145 | hp1 | a0002 | c0006 | t0001 | g0160 | AFR | ACB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | CDX | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | ACB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0163 | AFR | ACB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0138 | AMR | PEL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0162 | AFR | ACB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | KHV | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0172 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02602 | hp2 | a0004 | c0007 | t0002 | g0046 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0093 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02630 | hp2 | a0002 | c0006 | t0001 | g0159 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02647 | hp1 | a0004 | c0005 | t0002 | g0015 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02647 | hp2 | a0002 | c0006 | t0001 | g0168 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0127 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02698 | hp2 | a0008 | c0013 | t0001 | g0080 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02717 | hp1 | a0002 | c0006 | t0001 | g0044 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0010 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02809 | hp2 | a0005 | c0008 | t0002 | g0060 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0092 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02886 | hp2 | a0007 | c0012 | t0001 | g0077 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0173 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02896 | hp2 | a0005 | c0008 | t0001 | g0061 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0175 | AFR | ESN | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | ESN | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02976 | hp2 | a0002 | c0006 | t0001 | g0153 | AFR | ESN | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03098 | hp1 | a0003 | c0004 | t0002 | g0027 | AFR | MSL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | MSL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0152 | AFR | ESN | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03139 | hp2 | a0004 | c0005 | t0002 | g0042 | AFR | ESN | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0178 | AFR | ESN | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03195 | hp2 | a0002 | c0006 | t0001 | g0044 | AFR | ESN | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0024 | AFR | MSL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | MSL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0079 | AFR | MSL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03239 | hp1 | a0003 | c0004 | t0002 | g0007 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0109 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | MSL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | MSL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03490 | hp2 | a0004 | c0007 | t0002 | g0167 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03491 | hp1 | a0001 | c0003 | t0001 | g0010 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03491 | hp2 | a0001 | c0010 | t0001 | g0083 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0010 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03516 | hp1 | a0004 | c0005 | t0002 | g0015 | AFR | ESN | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0141 | AFR | ESN | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03540 | hp1 | a0004 | c0005 | t0002 | g0124 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03540 | hp2 | a0004 | c0005 | t0002 | g0015 | AFR | GWD | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0154 | AFR | MSL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | MSL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03704 | hp2 | a0003 | c0004 | t0002 | g0055 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03710 | hp1 | a0004 | c0005 | t0002 | g0078 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03710 | hp2 | a0001 | c0010 | t0001 | g0082 | SAS | PJL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0009 | SAS | BEB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03834 | hp1 | a0004 | c0007 | t0002 | g0046 | SAS | BEB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0010 | SAS | BEB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0147 | SAS | BEB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0136 | SAS | STU | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | STU | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG04204 | hp2 | a0001 | c0003 | t0001 | g0006 | SAS | STU | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG04228 | hp2 | a0004 | c0007 | t0002 | g0155 | SAS | STU | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | YRI | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18612 | hp1 | a0003 | c0004 | t0002 | g0007 | EAS | CHB | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | CHB | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18906 | hp1 | a0004 | c0005 | t0002 | g0114 | AFR | YRI | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18940 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18941 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18944 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18946 | hp2 | a0001 | c0003 | t0001 | g0157 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18947 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18956 | hp2 | a0003 | c0004 | t0003 | g0057 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18961 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18965 | hp2 | a0003 | c0004 | t0002 | g0058 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18968 | hp1 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18971 | hp1 | a0006 | c0009 | t0002 | g0029 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18978 | hp1 | a0003 | c0004 | t0003 | g0026 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18979 | hp2 | a0002 | c0011 | t0002 | g0146 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18985 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18988 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18989 | hp1 | a0003 | c0004 | t0002 | g0086 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18991 | hp1 | a0004 | c0005 | t0002 | g0110 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18993 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18993 | hp2 | a0003 | c0004 | t0002 | g0095 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18998 | hp1 | a0003 | c0004 | t0003 | g0059 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19003 | hp1 | a0001 | c0003 | t0001 | g0165 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19010 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19011 | hp2 | a0006 | c0009 | t0002 | g0029 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19030 | hp1 | a0002 | c0006 | t0001 | g0158 | AFR | LWK | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | LWK | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19054 | hp2 | a0003 | c0004 | t0002 | g0007 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19055 | hp1 | a0003 | c0004 | t0003 | g0026 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19055 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19057 | hp2 | a0003 | c0004 | t0002 | g0007 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19063 | hp1 | a0003 | c0004 | t0002 | g0007 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19064 | hp1 | a0003 | c0004 | t0002 | g0020 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19066 | hp2 | a0003 | c0004 | t0002 | g0056 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19067 | hp1 | a0003 | c0004 | t0002 | g0088 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19072 | hp2 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19075 | hp2 | a0003 | c0004 | t0002 | g0007 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19078 | hp1 | a0003 | c0004 | t0002 | g0007 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19081 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19240 | hp1 | a0004 | c0005 | t0002 | g0015 | AFR | YRI | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | YRI | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ASW | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA20129 | hp2 | a0002 | c0006 | t0001 | g0047 | AFR | ASW | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | TSI | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | GIH | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | GIH | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0161 | AFR | ACB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02486 | hp2 | a0009 | c0014 | t0001 | g0151 | AFR | ACB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | ACB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG02559 | hp2 | a0004 | c0005 | t0001 | g0125 | AFR | ACB | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0166 | AFR | MSL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG06807 | hp1 | a0002 | c0006 | t0001 | g0047 | AFR | USA | MDH1B_chr2_206732763_206770328 | MDH1B |
| HG06807 | hp2 | a0004 | c0005 | t0002 | g0042 | AFR | USA | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18955 | hp1 | a0003 | c0004 | t0002 | g0020 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | USA | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | USA | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | MDH1B_chr2_206732763_206770328 | MDH1B |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | LWK | MDH1B_chr2_206732763_206770328 | MDH1B |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0038 | REF | REF | MDH1B_chr2_206732763_206770328 | MDH1B |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0008 | REF | REF | MDH1B_chr2_206732763_206770328 | MDH1B |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:206738497
|
T | C | 3 | a0003a0004a0006 | 42 | HG00280.hp2 HG00642.hp2 HG01175.hp1 others(39): Show |
missense_variant | MODERATE | c.1543A>G | p.Thr515Ala | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 12/12 | 1600/2334 | 1543/1557 | 515/518 | chr2 | 206738497 | ||
| chr2:206738510
|
T | G | 5 | a0002a0003a0004others(2): Show | 143 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(140): Show |
missense_variant&splice_region_variant | MODERATE | c.1530A>C | p.Glu510Asp | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 12/12 | 1587/2334 | 1530/1557 | 510/518 | chr2 | 206738510 | ||
| chr2:206741062
|
A | G | 1 | a0007 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.1451T>C | p.Met484Thr | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 10/12 | 1508/2334 | 1451/1557 | 484/518 | chr2 | 206741062 | ||
| chr2:206751000
|
C | T | 3 | a0003a0005a0006 | 28 | HG01109.hp1 HG01175.hp1 HG01261.hp1 others(25): Show |
missense_variant | MODERATE | c.986G>A | p.Arg329Lys | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 6/12 | 1043/2334 | 986/1557 | 329/518 | chr2 | 206751000 | ||
| chr2:206755040
|
T | C | 1 | a0006 | 2 | NA18971.hp1 NA19011.hp2 |
missense_variant | MODERATE | c.879A>G | p.Ile293Met | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/12 | 936/2334 | 879/1557 | 293/518 | chr2 | 206755040 | ||
| chr2:206755218
|
G | C | 1 | a0008 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.701C>G | p.Pro234Arg | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/12 | 758/2334 | 701/1557 | 234/518 | chr2 | 206755218 | ||
| chr2:206755401
|
G | A | 1 | a0009 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.518C>T | p.Ala173Val | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/12 | 575/2334 | 518/1557 | 173/518 | chr2 | 206755401 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:206749141
|
C | T | 1 | a0002c0011 | 1 | NA18979.hp2 | synonymous_variant | LOW | c.1095G>A | p.Leu365Leu | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/12 | 1152/2334 | 1095/1557 | 365/518 | chr2 | 206749141 | ||
| chr2:206755055
|
A | G | 3 | a0001c0003a0002c0006a0004c0007 | 49 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(46): Show |
synonymous_variant | LOW | c.864T>C | p.Gly288Gly | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/12 | 921/2334 | 864/1557 | 288/518 | chr2 | 206755055 | ||
| chr2:206757348
|
T | C | 1 | a0001c0010 | 2 | HG03491.hp2 HG03710.hp2 |
synonymous_variant | LOW | c.159A>G | p.Glu53Glu | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 3/12 | 216/2334 | 159/1557 | 53/518 | chr2 | 206757348 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:206737814
|
A | G | 1 | a0001c0003t0004 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*669T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 12/12 | 669 | chr2 | 206737814 | |||||
| chr2:206738166
|
G | T | 8 | a0002c0002t0002a0002c0011t0002a0003c0004t0002others(5): Show | 111 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*317C>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 12/12 | 317 | chr2 | 206738166 | |||||
| chr2:206738425
|
ATTCT | A | 1 | a0003c0004t0003 | 4 | NA18956.hp2 NA18978.hp1 NA18998.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*54_*57delAGAA | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 12/12 | 54 | chr2 | 206738425 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:206738606
|
T | C | 4 | a0001c0003t0001g0006a0001c0003t0001g0048a0001c0003t0001g0165others(1): Show | 14 | HG02056.hp2 HG02135.hp2 HG04204.hp2 others(11): Show |
intron_variant | MODIFIER | c.1529-95A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 11/11 | chr2 | 206738606 | ||||||
| chr2:206738627
|
A | C | 2 | a0002c0002t0001g0092a0002c0002t0001g0093 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1529-116T>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 11/11 | chr2 | 206738627 | ||||||
| chr2:206738633
|
A | G | 2 | a0002c0002t0001g0017a0002c0002t0001g0178 | 5 | HG01069.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1529-122T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 11/11 | chr2 | 206738633 | ||||||
| chr2:206738733
|
A | G | 3 | a0002c0006t0001g0044a0002c0006t0001g0160a0005c0008t0001g0061 | 4 | HG02145.hp1 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1529-222T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 11/11 | chr2 | 206738733 | ||||||
| chr2:206738750
|
C | T | 37 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0009others(34): Show | 70 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.1529-239G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 11/11 | chr2 | 206738750 | ||||||
| chr2:206738813
|
C | CTT | 79 | a0002c0002t0001g0017a0002c0002t0001g0019a0002c0002t0001g0079others(76): Show | 137 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.1529-303_1529-302i others(4): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 11/11 | chr2 | 206738813 | ||||||
| chr2:206738905
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1529-394C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 11/11 | chr2 | 206738905 | ||||||
| chr2:206738928
|
T | A | 1 | a0002c0002t0002g0136 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1529-417A>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 11/11 | chr2 | 206738928 | ||||||
| chr2:206738957
|
G | A | 1 | a0001c0003t0001g0023 | 3 | HG02559.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1529-446C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 11/11 | chr2 | 206738957 | ||||||
| chr2:206739259
|
A | G | 2 | a0002c0006t0001g0160a0005c0008t0001g0061 | 2 | HG02145.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1528+334T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 11/11 | chr2 | 206739259 | ||||||
| chr2:206739406
|
T | C | 81 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(78): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1528+187A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 11/11 | chr2 | 206739406 | ||||||
| chr2:206739415
|
A | G | 1 | a0002c0002t0001g0141 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1528+178T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 11/11 | chr2 | 206739415 | ||||||
| chr2:206739506
|
T | C | 1 | a0001c0001t0001g0033 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1528+87A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 11/11 | chr2 | 206739506 | ||||||
| chr2:206739509
|
T | C | 1 | a0002c0002t0002g0144 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1528+84A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 11/11 | chr2 | 206739509 | ||||||
| chr2:206739702
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1460-41G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 10/11 | chr2 | 206739702 | ||||||
| chr2:206739703
|
G | A | 23 | a0003c0004t0002g0007a0003c0004t0002g0020a0003c0004t0002g0027others(20): Show | 41 | HG00280.hp2 HG00642.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.1460-42C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 10/11 | chr2 | 206739703 | ||||||
| chr2:206739908
|
C | G | 1 | a0001c0001t0001g0034 | 2 | NA20752.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1460-247G>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 10/11 | chr2 | 206739908 | ||||||
| chr2:206740123
|
T | C | 1 | a0002c0002t0001g0172 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1460-462A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 10/11 | chr2 | 206740123 | ||||||
| chr2:206740131
|
G | C | 2 | a0002c0002t0001g0017a0002c0002t0001g0178 | 5 | HG01069.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1460-470C>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 10/11 | chr2 | 206740131 | ||||||
| chr2:206740157
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1460-496T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 10/11 | chr2 | 206740157 | ||||||
| chr2:206740193
|
C | T | 78 | a0002c0002t0001g0017a0002c0002t0001g0019a0002c0002t0001g0079others(75): Show | 136 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1460-532G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 10/11 | chr2 | 206740193 | ||||||
| chr2:206740530
|
C | T | 10 | a0002c0002t0001g0079a0002c0002t0001g0172a0002c0006t0001g0044others(7): Show | 12 | HG02145.hp1 HG02572.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1459+524G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 10/11 | chr2 | 206740530 | ||||||
| chr2:206740605
|
A | G | 7 | a0002c0002t0001g0079a0002c0002t0001g0172a0002c0006t0001g0047others(4): Show | 8 | HG02572.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1459+449T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 10/11 | chr2 | 206740605 | ||||||
| chr2:206740684
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1459+370G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 10/11 | chr2 | 206740684 | ||||||
| chr2:206740686
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0063 | 4 | HG01361.hp2 HG01433.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1459+368G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 10/11 | chr2 | 206740686 | ||||||
| chr2:206740886
|
A | C | 78 | a0002c0002t0001g0017a0002c0002t0001g0019a0002c0002t0001g0079others(75): Show | 136 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1459+168T>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 10/11 | chr2 | 206740886 | ||||||
| chr2:206740963
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1459+91G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 10/11 | chr2 | 206740963 | ||||||
| chr2:206741009
|
C | T | 81 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(78): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1459+45G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 10/11 | chr2 | 206741009 | ||||||
| chr2:206741158
|
A | G | 81 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(78): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1409-54T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206741158 | ||||||
| chr2:206741252
|
T | C | 81 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(78): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1409-148A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206741252 | ||||||
| chr2:206741370
|
A | G | 81 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(78): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1409-266T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206741370 | ||||||
| chr2:206741475
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1409-371G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206741475 | ||||||
| chr2:206741542
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0069 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1409-438T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206741542 | ||||||
| chr2:206741626
|
G | T | 78 | a0002c0002t0001g0017a0002c0002t0001g0019a0002c0002t0001g0079others(75): Show | 136 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1409-522C>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206741626 | ||||||
| chr2:206741643
|
A | C | 81 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(78): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1409-539T>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206741643 | ||||||
| chr2:206741651
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1409-547A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206741651 | ||||||
| chr2:206741941
|
A | T | 1 | a0001c0001t0001g0122 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1409-837T>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206741941 | ||||||
| chr2:206741955
|
A | C | 81 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(78): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1409-851T>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206741955 | ||||||
| chr2:206742030
|
TGTG | T | 23 | a0003c0004t0002g0007a0003c0004t0002g0020a0003c0004t0002g0027others(20): Show | 41 | HG00280.hp2 HG00642.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.1409-929_1409-927d others(5): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742030 | ||||||
| chr2:206742049
|
T | C | 2 | a0002c0002t0001g0017a0002c0002t0001g0178 | 5 | HG01069.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1409-945A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742049 | ||||||
| chr2:206742105
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1409-1001T>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742105 | ||||||
| chr2:206742113
|
A | G | 81 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(78): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1409-1009T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742113 | ||||||
| chr2:206742241
|
T | C | 81 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(78): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1409-1137A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742241 | ||||||
| chr2:206742253
|
G | A | 2 | a0002c0002t0001g0017a0002c0002t0001g0178 | 5 | HG01069.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1409-1149C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742253 | ||||||
| chr2:206742460
|
C | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0150 | 2 | NA18970.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1409-1356G>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742460 | ||||||
| chr2:206742694
|
AGC | A | 81 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(78): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1409-1592_1409-159 others(6): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742694 | ||||||
| chr2:206742711
|
A | AT | 10 | a0001c0001t0001g0011a0001c0001t0001g0032a0001c0001t0001g0041others(7): Show | 15 | HG00741.hp2 HG01175.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.1409-1608dupA | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742711 | ||||||
| chr2:206742711
|
AT | A | 14 | a0001c0001t0001g0049a0001c0001t0001g0072a0001c0001t0001g0123others(11): Show | 15 | HG00544.hp2 HG02027.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.1409-1608delA | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742711 | ||||||
| chr2:206742711
|
ATT | A | 46 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0003t0001g0023others(43): Show | 89 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.1409-1609_1409-160 others(6): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742711 | ||||||
| chr2:206742711
|
ATTT | A | 36 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0024others(33): Show | 71 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.1409-1610_1409-160 others(7): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742711 | ||||||
| chr2:206742711
|
ATTTT | A | 5 | a0001c0003t0001g0165a0002c0002t0001g0019a0002c0002t0001g0085others(2): Show | 7 | HG02055.hp1 HG02145.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1409-1611_1409-160 others(8): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742711 | ||||||
| chr2:206742751
|
C | A | 1 | a0001c0001t0001g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1409-1647G>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742751 | ||||||
| chr2:206742795
|
T | G | 1 | a0001c0001t0001g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1409-1691A>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742795 | ||||||
| chr2:206742812
|
C | T | 1 | a0002c0002t0001g0093 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1409-1708G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742812 | ||||||
| chr2:206742814
|
T | C | 123 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0025others(120): Show | 234 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1409-1710A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742814 | ||||||
| chr2:206742825
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1409-1721G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742825 | ||||||
| chr2:206742868
|
T | C | 1 | a0002c0002t0002g0134 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1409-1764A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742868 | ||||||
| chr2:206742906
|
A | G | 67 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0033others(64): Show | 126 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.1409-1802T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742906 | ||||||
| chr2:206742916
|
C | T | 40 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0033others(37): Show | 87 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1409-1812G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742916 | ||||||
| chr2:206742917
|
A | G | 40 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0033others(37): Show | 87 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1409-1813T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742917 | ||||||
| chr2:206742920
|
T | C | 1 | a0001c0003t0001g0163 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1409-1816A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742920 | ||||||
| chr2:206742927
|
G | A | 4 | a0004c0007t0002g0045a0004c0007t0002g0046a0004c0007t0002g0155others(1): Show | 6 | HG00280.hp2 HG00642.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.1409-1823C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742927 | ||||||
| chr2:206742962
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0150 | 2 | NA18970.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1409-1858T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742962 | ||||||
| chr2:206742966
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0150 | 2 | NA18970.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1409-1862G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742966 | ||||||
| chr2:206742970
|
C | G | 1 | a0002c0002t0001g0172 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1409-1866G>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742970 | ||||||
| chr2:206742994
|
T | C | 2 | a0005c0008t0002g0051a0005c0008t0002g0060 | 2 | HG01109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1409-1890A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206742994 | ||||||
| chr2:206743005
|
A | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0112a0001c0001t0001g0121others(1): Show | 7 | HG02165.hp1 NA18747.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1409-1901T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206743005 | ||||||
| chr2:206743048
|
G | T | 1 | a0004c0007t0002g0167 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1409-1944C>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206743048 | ||||||
| chr2:206743073
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0090a0001c0001t0001g0091 | 4 | HG01243.hp2 HG02965.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1409-1969C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206743073 | ||||||
| chr2:206743458
|
C | T | 1 | a0004c0005t0002g0042 | 2 | HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1408+2164G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206743458 | ||||||
| chr2:206743736
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1408+1886T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206743736 | ||||||
| chr2:206743738
|
C | A | 1 | a0004c0005t0002g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1408+1884G>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206743738 | ||||||
| chr2:206743785
|
T | A | 79 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(76): Show | 140 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1408+1837A>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206743785 | ||||||
| chr2:206743785
|
T | G | 1 | a0002c0002t0002g0135 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1408+1837A>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206743785 | ||||||
| chr2:206743788
|
T | C | 1 | a0002c0002t0002g0104 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1408+1834A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206743788 | ||||||
| chr2:206743819
|
T | C | 81 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(78): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1408+1803A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206743819 | ||||||
| chr2:206743871
|
T | G | 81 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(78): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1408+1751A>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206743871 | ||||||
| chr2:206744132
|
C | A | 1 | a0001c0001t0001g0062 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1408+1490G>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206744132 | ||||||
| chr2:206744224
|
C | T | 15 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(12): Show | 38 | HG00423.hp2 HG01255.hp1 HG02027.hp2 others(35): Show |
intron_variant | MODIFIER | c.1408+1398G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206744224 | ||||||
| chr2:206744288
|
G | C | 1 | a0001c0001t0001g0097 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1408+1334C>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206744288 | ||||||
| chr2:206744815
|
A | C | 81 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(78): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1408+807T>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206744815 | ||||||
| chr2:206744919
|
T | C | 81 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(78): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1408+703A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206744919 | ||||||
| chr2:206744945
|
AAT | A | 4 | a0002c0002t0002g0009a0002c0002t0002g0135a0002c0002t0002g0136others(1): Show | 10 | HG02015.hp1 HG03831.hp1 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.1408+675_1408+676d others(4): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206744945 | ||||||
| chr2:206744947
|
T | A | 77 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(74): Show | 132 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.1408+675A>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206744947 | ||||||
| chr2:206744948
|
A | AAT | 5 | a0002c0002t0001g0019a0002c0002t0001g0085a0002c0002t0001g0141others(2): Show | 8 | HG00408.hp1 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1408+673_1408+674i others(4): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206744948 | ||||||
| chr2:206744950
|
A | AAT | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0025others(23): Show | 56 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1408+670_1408+671d others(4): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206744950 | ||||||
| chr2:206744950
|
A | T | 73 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(70): Show | 127 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1408+672T>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206744950 | ||||||
| chr2:206745133
|
G | A | 1 | a0001c0001t0001g0034 | 2 | NA20752.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1408+489C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206745133 | ||||||
| chr2:206745272
|
G | A | 1 | a0001c0001t0001g0035 | 2 | HG00639.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1408+350C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206745272 | ||||||
| chr2:206745305
|
C | T | 4 | a0002c0002t0001g0016a0002c0002t0001g0173a0002c0002t0001g0175others(1): Show | 8 | HG02258.hp1 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1408+317G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206745305 | ||||||
| chr2:206745323
|
C | T | 60 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0009others(57): Show | 111 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.1408+299G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 9/11 | chr2 | 206745323 | ||||||
| chr2:206745730
|
CTTT | C | 3 | a0002c0002t0001g0017a0002c0002t0001g0178a0002c0002t0002g0132 | 6 | HG01069.hp2 HG01192.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1357-60_1357-58del others(3): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 8/11 | chr2 | 206745730 | ||||||
| chr2:206745730
|
CTTTT | C | 77 | a0002c0002t0001g0016a0002c0002t0001g0019a0002c0002t0001g0079others(74): Show | 135 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.1357-61_1357-58del others(4): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 8/11 | chr2 | 206745730 | ||||||
| chr2:206745874
|
T | C | 81 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(78): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1357-201A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 8/11 | chr2 | 206745874 | ||||||
| chr2:206745961
|
C | T | 81 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(78): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1357-288G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 8/11 | chr2 | 206745961 | ||||||
| chr2:206746020
|
A | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0025others(23): Show | 56 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1356+267T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 8/11 | chr2 | 206746020 | ||||||
| chr2:206746079
|
C | T | 81 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(78): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1356+208G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 8/11 | chr2 | 206746079 | ||||||
| chr2:206746098
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1356+189A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 8/11 | chr2 | 206746098 | ||||||
| chr2:206746121
|
G | A | 65 | a0002c0002t0001g0016a0002c0002t0001g0019a0002c0002t0001g0079others(62): Show | 111 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.1356+166C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 8/11 | chr2 | 206746121 | ||||||
| chr2:206746131
|
C | G | 1 | a0002c0006t0001g0158 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1356+156G>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 8/11 | chr2 | 206746131 | ||||||
| chr2:206746131
|
C | T | 2 | a0002c0002t0001g0092a0002c0002t0001g0093 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1356+156G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 8/11 | chr2 | 206746131 | ||||||
| chr2:206746185
|
A | C | 81 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0019others(78): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1356+102T>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 8/11 | chr2 | 206746185 | ||||||
| chr2:206746224
|
C | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0116 | 2 | HG01175.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1356+63G>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 8/11 | chr2 | 206746224 | ||||||
| chr2:206746480
|
C | T | 1 | a0005c0008t0002g0051 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1217-54G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206746480 | ||||||
| chr2:206746506
|
T | G | 88 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(85): Show | 164 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1217-80A>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206746506 | ||||||
| chr2:206746533
|
G | T | 47 | a0002c0002t0001g0017a0002c0002t0001g0019a0002c0002t0001g0085others(44): Show | 86 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1217-107C>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206746533 | ||||||
| chr2:206746556
|
C | T | 2 | a0001c0003t0001g0162a0001c0003t0001g0166 | 2 | HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1217-130G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206746556 | ||||||
| chr2:206746617
|
C | T | 15 | a0003c0004t0002g0007a0003c0004t0002g0020a0003c0004t0002g0027others(12): Show | 27 | HG01109.hp1 HG01175.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.1217-191G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206746617 | ||||||
| chr2:206746705
|
T | C | 20 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0003t0001g0006others(17): Show | 43 | HG00423.hp2 HG01081.hp1 HG01255.hp1 others(40): Show |
intron_variant | MODIFIER | c.1217-279A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206746705 | ||||||
| chr2:206746751
|
G | A | 2 | a0002c0002t0001g0092a0002c0002t0001g0093 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1217-325C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206746751 | ||||||
| chr2:206746784
|
T | G | 1 | a0001c0001t0001g0043 | 2 | NA18962.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1217-358A>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206746784 | ||||||
| chr2:206746872
|
C | G | 1 | a0001c0001t0001g0030 | 2 | HG04184.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1217-446G>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206746872 | ||||||
| chr2:206746900
|
G | A | 1 | a0009c0014t0001g0151 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1217-474C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206746900 | ||||||
| chr2:206747090
|
T | C | 12 | a0003c0004t0002g0007a0003c0004t0002g0020a0003c0004t0002g0055others(9): Show | 23 | HG01175.hp1 HG02129.hp1 HG03239.hp1 others(20): Show |
intron_variant | MODIFIER | c.1217-664A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206747090 | ||||||
| chr2:206747102
|
G | A | 52 | a0001c0001t0001g0036a0001c0001t0001g0090a0001c0001t0001g0091others(49): Show | 93 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1217-676C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206747102 | ||||||
| chr2:206747124
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1217-698A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206747124 | ||||||
| chr2:206747156
|
C | CA | 132 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(129): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.1217-731dupT | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206747156 | ||||||
| chr2:206747164
|
C | A | 1 | a0001c0001t0001g0075 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1217-738G>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206747164 | ||||||
| chr2:206747165
|
A | AAAC | 4 | a0001c0001t0001g0049a0001c0001t0001g0066a0001c0001t0001g0094others(1): Show | 5 | HG00738.hp1 HG02523.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1217-742_1217-740d others(5): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206747165 | ||||||
| chr2:206747234
|
T | C | 1 | a0004c0007t0002g0167 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1217-808A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206747234 | ||||||
| chr2:206747404
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0036others(109): Show | 209 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.1217-978G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206747404 | ||||||
| chr2:206747549
|
TTGAG | T | 30 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(27): Show | 56 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.1217-1127_1217-112 others(8): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206747549 | ||||||
| chr2:206747700
|
C | T | 28 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(25): Show | 54 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1217-1274G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206747700 | ||||||
| chr2:206747709
|
T | A | 28 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(25): Show | 54 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1217-1283A>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206747709 | ||||||
| chr2:206747724
|
C | T | 5 | a0002c0006t0001g0047a0002c0006t0001g0153a0002c0006t0001g0158others(2): Show | 6 | HG02630.hp2 HG02647.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1216+1296G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206747724 | ||||||
| chr2:206747776
|
T | C | 1 | a0002c0002t0002g0111 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1216+1244A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206747776 | ||||||
| chr2:206747790
|
G | A | 1 | a0001c0001t0001g0049 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1216+1230C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206747790 | ||||||
| chr2:206747825
|
TATAAC | T | 28 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(25): Show | 54 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1216+1190_1216+119 others(9): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206747825 | ||||||
| chr2:206747881
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1216+1139C>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206747881 | ||||||
| chr2:206747889
|
T | C | 28 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(25): Show | 54 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1216+1131A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206747889 | ||||||
| chr2:206747917
|
TC | T | 28 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(25): Show | 54 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1216+1102delG | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206747917 | ||||||
| chr2:206748155
|
T | C | 28 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(25): Show | 54 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1216+865A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206748155 | ||||||
| chr2:206748221
|
A | G | 1 | a0004c0005t0002g0114 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1216+799T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206748221 | ||||||
| chr2:206748248
|
A | G | 29 | a0001c0001t0001g0169a0001c0003t0001g0006a0001c0003t0001g0010others(26): Show | 55 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1216+772T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206748248 | ||||||
| chr2:206748281
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(53): Show | 138 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.1216+739C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206748281 | ||||||
| chr2:206748373
|
C | T | 28 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(25): Show | 54 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1216+647G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206748373 | ||||||
| chr2:206748403
|
T | A | 1 | a0001c0001t0001g0091 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1216+617A>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206748403 | ||||||
| chr2:206748466
|
G | A | 1 | a0002c0002t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1216+554C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206748466 | ||||||
| chr2:206748521
|
G | GGGTC | 2 | a0001c0001t0001g0012a0001c0001t0001g0087 | 5 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1216+495_1216+498d others(6): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206748521 | ||||||
| chr2:206748585
|
G | T | 1 | a0002c0002t0002g0147 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1216+435C>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206748585 | ||||||
| chr2:206748616
|
A | C | 29 | a0001c0001t0001g0169a0001c0003t0001g0006a0001c0003t0001g0010others(26): Show | 55 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1216+404T>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206748616 | ||||||
| chr2:206748633
|
G | C | 1 | a0001c0003t0001g0023 | 3 | HG02559.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1216+387C>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206748633 | ||||||
| chr2:206748637
|
A | C | 1 | a0003c0004t0002g0020 | 3 | HG02129.hp1 NA18955.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1216+383T>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206748637 | ||||||
| chr2:206748777
|
A | T | 28 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(25): Show | 54 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1216+243T>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206748777 | ||||||
| chr2:206748822
|
G | A | 1 | a0002c0002t0002g0138 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1216+198C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206748822 | ||||||
| chr2:206748888
|
G | T | 26 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(23): Show | 49 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.1216+132C>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206748888 | ||||||
| chr2:206748966
|
G | C | 28 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(25): Show | 54 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1216+54C>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206748966 | ||||||
| chr2:206748997
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1216+23T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 7/11 | chr2 | 206748997 | ||||||
| chr2:206749256
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(100): Show | 217 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1053-73C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 6/11 | chr2 | 206749256 | ||||||
| chr2:206749498
|
T | A | 7 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0048others(4): Show | 22 | HG00423.hp2 HG01255.hp1 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.1053-315A>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 6/11 | chr2 | 206749498 | ||||||
| chr2:206749842
|
A | C | 1 | a0002c0002t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1053-659T>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 6/11 | chr2 | 206749842 | ||||||
| chr2:206749998
|
A | G | 1 | a0002c0002t0002g0119 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1053-815T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 6/11 | chr2 | 206749998 | ||||||
| chr2:206750096
|
C | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0038others(103): Show | 201 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1052+838G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 6/11 | chr2 | 206750096 | ||||||
| chr2:206750288
|
A | C | 1 | a0002c0002t0002g0118 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1052+646T>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 6/11 | chr2 | 206750288 | ||||||
| chr2:206750289
|
T | C | 29 | a0001c0001t0001g0169a0001c0003t0001g0006a0001c0003t0001g0010others(26): Show | 55 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1052+645A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 6/11 | chr2 | 206750289 | ||||||
| chr2:206750395
|
T | A | 27 | a0001c0001t0001g0169a0001c0003t0001g0006a0001c0003t0001g0010others(24): Show | 50 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.1052+539A>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 6/11 | chr2 | 206750395 | ||||||
| chr2:206750397
|
A | T | 3 | a0002c0002t0002g0102a0002c0002t0002g0117a0002c0011t0002g0146 | 3 | NA18979.hp2 NA19063.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1052+537T>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 6/11 | chr2 | 206750397 | ||||||
| chr2:206750560
|
C | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0038others(73): Show | 145 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1052+374G>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 6/11 | chr2 | 206750560 | ||||||
| chr2:206750649
|
A | G | 1 | a0002c0002t0002g0115 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1052+285T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 6/11 | chr2 | 206750649 | ||||||
| chr2:206750768
|
T | C | 29 | a0001c0001t0001g0169a0001c0003t0001g0006a0001c0003t0001g0010others(26): Show | 55 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1052+166A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 6/11 | chr2 | 206750768 | ||||||
| chr2:206750798
|
G | C | 29 | a0001c0001t0001g0169a0001c0003t0001g0006a0001c0003t0001g0010others(26): Show | 55 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1052+136C>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 6/11 | chr2 | 206750798 | ||||||
| chr2:206750927
|
A | G | 1 | a0002c0002t0001g0175 | 1 | HG02922.hp1 | splice_region_variant&intron_variant | LOW | c.1052+7T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 6/11 | chr2 | 206750927 | ||||||
| chr2:206751086
|
T | C | 6 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0090others(3): Show | 8 | HG00738.hp1 HG01243.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.911-11A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206751086 | ||||||
| chr2:206751133
|
G | A | 28 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(25): Show | 54 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.911-58C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206751133 | ||||||
| chr2:206751139
|
A | G | 1 | a0002c0002t0002g0040 | 2 | HG00408.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.911-64T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206751139 | ||||||
| chr2:206751200
|
T | A | 1 | a0001c0001t0001g0139 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.911-125A>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206751200 | ||||||
| chr2:206751292
|
G | C | 1 | a0001c0001t0001g0090 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.911-217C>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206751292 | ||||||
| chr2:206751601
|
A | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0036others(73): Show | 143 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.911-526T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206751601 | ||||||
| chr2:206751756
|
A | C | 1 | a0001c0003t0001g0157 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.911-681T>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206751756 | ||||||
| chr2:206751837
|
A | G | 29 | a0001c0001t0001g0169a0001c0003t0001g0006a0001c0003t0001g0010others(26): Show | 55 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.911-762T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206751837 | ||||||
| chr2:206751922
|
T | C | 1 | a0002c0002t0002g0140 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.911-847A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206751922 | ||||||
| chr2:206751928
|
G | T | 1 | a0004c0005t0002g0114 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.911-853C>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206751928 | ||||||
| chr2:206751944
|
C | T | 1 | a0002c0002t0002g0113 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.911-869G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206751944 | ||||||
| chr2:206751985
|
T | C | 29 | a0001c0001t0001g0169a0001c0003t0001g0006a0001c0003t0001g0010others(26): Show | 55 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.911-910A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206751985 | ||||||
| chr2:206752012
|
G | T | 27 | a0001c0001t0001g0169a0001c0003t0001g0006a0001c0003t0001g0010others(24): Show | 50 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.911-937C>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206752012 | ||||||
| chr2:206752160
|
G | C | 29 | a0001c0001t0001g0169a0001c0003t0001g0006a0001c0003t0001g0010others(26): Show | 55 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.911-1085C>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206752160 | ||||||
| chr2:206752314
|
G | T | 1 | a0001c0001t0001g0169 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.911-1239C>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206752314 | ||||||
| chr2:206752376
|
C | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(58): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.911-1301G>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206752376 | ||||||
| chr2:206752419
|
G | A | 1 | a0002c0002t0001g0141 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.911-1344C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206752419 | ||||||
| chr2:206752613
|
C | T | 27 | a0001c0001t0001g0169a0001c0003t0001g0006a0001c0003t0001g0010others(24): Show | 50 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.911-1538G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206752613 | ||||||
| chr2:206752633
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.911-1558G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206752633 | ||||||
| chr2:206752656
|
C | G | 29 | a0001c0001t0001g0169a0001c0003t0001g0006a0001c0003t0001g0010others(26): Show | 55 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.911-1581G>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206752656 | ||||||
| chr2:206752711
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.911-1636G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206752711 | ||||||
| chr2:206752749
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.911-1674C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206752749 | ||||||
| chr2:206752792
|
CT | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(132): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.911-1718delA | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206752792 | ||||||
| chr2:206752792
|
CTT | C | 31 | a0001c0001t0001g0169a0001c0003t0001g0006a0001c0003t0001g0010others(28): Show | 57 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.911-1719_911-1718d others(4): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206752792 | ||||||
| chr2:206752872
|
C | T | 1 | a0001c0003t0001g0156 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.911-1797G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206752872 | ||||||
| chr2:206753112
|
T | G | 1 | a0001c0003t0001g0166 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.910+1897A>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206753112 | ||||||
| chr2:206753129
|
G | GATCA | 29 | a0001c0001t0001g0169a0001c0003t0001g0006a0001c0003t0001g0010others(26): Show | 55 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.910+1876_910+1879d others(6): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206753129 | ||||||
| chr2:206753147
|
A | T | 12 | a0003c0004t0002g0007a0003c0004t0002g0020a0003c0004t0002g0055others(9): Show | 23 | HG01175.hp1 HG02129.hp1 HG03239.hp1 others(20): Show |
intron_variant | MODIFIER | c.910+1862T>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206753147 | ||||||
| chr2:206753190
|
C | A | 2 | a0004c0007t0002g0046a0004c0007t0002g0155 | 3 | HG02602.hp2 HG03834.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.910+1819G>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206753190 | ||||||
| chr2:206753452
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.910+1557G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206753452 | ||||||
| chr2:206753459
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(92): Show | 208 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.910+1550G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206753459 | ||||||
| chr2:206753547
|
G | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(59): Show | 146 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.910+1462C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206753547 | ||||||
| chr2:206753823
|
C | G | 1 | a0001c0001t0001g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.910+1186G>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206753823 | ||||||
| chr2:206753868
|
C | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(54): Show | 139 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.910+1141G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206753868 | ||||||
| chr2:206753911
|
T | G | 1 | a0002c0002t0002g0145 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.910+1098A>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206753911 | ||||||
| chr2:206753926
|
T | C | 1 | a0002c0002t0002g0145 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.910+1083A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206753926 | ||||||
| chr2:206753978
|
T | G | 29 | a0001c0001t0001g0169a0001c0003t0001g0006a0001c0003t0001g0010others(26): Show | 55 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.910+1031A>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206753978 | ||||||
| chr2:206754197
|
A | G | 26 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(23): Show | 49 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.910+812T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206754197 | ||||||
| chr2:206754296
|
G | T | 2 | a0001c0001t0001g0049a0009c0014t0001g0151 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.910+713C>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206754296 | ||||||
| chr2:206754324
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.910+685T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206754324 | ||||||
| chr2:206754443
|
G | A | 26 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(23): Show | 49 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.910+566C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206754443 | ||||||
| chr2:206754500
|
G | A | 26 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(23): Show | 49 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.910+509C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206754500 | ||||||
| chr2:206754504
|
T | C | 1 | a0002c0002t0002g0109 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.910+505A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206754504 | ||||||
| chr2:206754608
|
G | A | 1 | a0009c0014t0001g0151 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.910+401C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206754608 | ||||||
| chr2:206754710
|
T | C | 4 | a0004c0007t0002g0045a0004c0007t0002g0046a0004c0007t0002g0155others(1): Show | 6 | HG00280.hp2 HG00642.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.910+299A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206754710 | ||||||
| chr2:206754739
|
C | T | 3 | a0004c0007t0002g0045a0004c0007t0002g0046a0004c0007t0002g0155 | 5 | HG00280.hp2 HG00642.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.910+270G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206754739 | ||||||
| chr2:206754834
|
G | A | 26 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(23): Show | 49 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.910+175C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206754834 | ||||||
| chr2:206754949
|
C | A | 1 | a0002c0006t0001g0044 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.910+60G>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 5/11 | chr2 | 206754949 | ||||||
| chr2:206755606
|
T | C | 26 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(23): Show | 49 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.414-101A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 4/11 | chr2 | 206755606 | ||||||
| chr2:206755638
|
C | A | 26 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(23): Show | 49 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.414-133G>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 4/11 | chr2 | 206755638 | ||||||
| chr2:206755689
|
C | A | 1 | a0001c0001t0001g0081 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.414-184G>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 4/11 | chr2 | 206755689 | ||||||
| chr2:206755794
|
A | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0038others(70): Show | 142 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.414-289T>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 4/11 | chr2 | 206755794 | ||||||
| chr2:206755875
|
C | G | 2 | a0002c0002t0001g0019a0002c0002t0001g0085 | 4 | HG02055.hp1 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.414-370G>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 4/11 | chr2 | 206755875 | ||||||
| chr2:206755891
|
A | G | 1 | a0004c0005t0002g0110 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.414-386T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 4/11 | chr2 | 206755891 | ||||||
| chr2:206755915
|
CTT | C | 26 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(23): Show | 49 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.414-412_414-411del others(2): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 4/11 | chr2 | 206755915 | ||||||
| chr2:206756079
|
T | C | 27 | a0001c0001t0001g0169a0001c0003t0001g0006a0001c0003t0001g0010others(24): Show | 50 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.414-574A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 4/11 | chr2 | 206756079 | ||||||
| chr2:206756131
|
G | C | 1 | a0001c0001t0001g0049 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.414-626C>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 4/11 | chr2 | 206756131 | ||||||
| chr2:206756179
|
T | C | 1 | a0001c0001t0001g0049 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.414-674A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 4/11 | chr2 | 206756179 | ||||||
| chr2:206756326
|
C | T | 1 | a0002c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.413+572G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 4/11 | chr2 | 206756326 | ||||||
| chr2:206756404
|
A | G | 1 | a0002c0006t0001g0044 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.413+494T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 4/11 | chr2 | 206756404 | ||||||
| chr2:206756416
|
T | C | 26 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(23): Show | 49 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.413+482A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 4/11 | chr2 | 206756416 | ||||||
| chr2:206756685
|
A | G | 26 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(23): Show | 49 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.413+213T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 4/11 | chr2 | 206756685 | ||||||
| chr2:206756742
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0090a0001c0001t0001g0091 | 4 | HG01243.hp2 HG02965.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+156C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 4/11 | chr2 | 206756742 | ||||||
| chr2:206757683
|
C | G | 1 | a0003c0004t0002g0095 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.136-312G>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206757683 | ||||||
| chr2:206757778
|
A | T | 28 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(25): Show | 54 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.136-407T>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206757778 | ||||||
| chr2:206757794
|
G | T | 1 | a0002c0002t0002g0109 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.136-423C>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206757794 | ||||||
| chr2:206757813
|
A | T | 3 | a0002c0002t0001g0017a0002c0002t0001g0175a0002c0002t0001g0178 | 6 | HG01069.hp2 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.136-442T>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206757813 | ||||||
| chr2:206757819
|
T | C | 28 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(25): Show | 54 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.136-448A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206757819 | ||||||
| chr2:206757877
|
C | A | 1 | a0002c0011t0002g0146 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.136-506G>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206757877 | ||||||
| chr2:206758048
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.136-677T>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206758048 | ||||||
| chr2:206758162
|
T | C | 1 | a0002c0002t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.136-791A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206758162 | ||||||
| chr2:206758248
|
A | G | 26 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(23): Show | 49 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.136-877T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206758248 | ||||||
| chr2:206758563
|
C | T | 2 | a0001c0001t0001g0170a0002c0002t0001g0152 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.136-1192G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206758563 | ||||||
| chr2:206758623
|
A | G | 28 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(25): Show | 54 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.136-1252T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206758623 | ||||||
| chr2:206758754
|
G | A | 1 | a0002c0002t0001g0152 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.136-1383C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206758754 | ||||||
| chr2:206758771
|
C | CAAAAAA | 28 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(25): Show | 54 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.136-1401_136-1400i others(8): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206758771 | ||||||
| chr2:206758775
|
C | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0036others(108): Show | 208 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.136-1404G>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206758775 | ||||||
| chr2:206758777
|
C | A | 83 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0036others(80): Show | 154 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.136-1406G>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206758777 | ||||||
| chr2:206758779
|
C | A | 28 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(25): Show | 54 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.136-1408G>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206758779 | ||||||
| chr2:206758781
|
C | A | 84 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(81): Show | 157 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.136-1410G>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206758781 | ||||||
| chr2:206758783
|
A | C | 20 | a0001c0001t0001g0018a0001c0001t0001g0028a0002c0002t0001g0019others(17): Show | 37 | HG00735.hp2 HG01074.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.136-1412T>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206758783 | ||||||
| chr2:206758785
|
A | C | 1 | a0002c0002t0002g0108 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.136-1414T>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206758785 | ||||||
| chr2:206758856
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.136-1485A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206758856 | ||||||
| chr2:206758906
|
G | C | 8 | a0001c0001t0001g0050a0001c0001t0001g0169a0001c0001t0001g0174others(5): Show | 9 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-1535C>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206758906 | ||||||
| chr2:206758942
|
C | T | 1 | a0001c0003t0001g0023 | 3 | HG02559.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.136-1571G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206758942 | ||||||
| chr2:206758960
|
TTTG | T | 27 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(24): Show | 53 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.136-1592_136-1590d others(5): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206758960 | ||||||
| chr2:206758963
|
G | T | 7 | a0001c0001t0001g0018a0001c0001t0001g0036a0001c0001t0001g0090others(4): Show | 10 | HG00408.hp2 HG00735.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.136-1592C>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206758963 | ||||||
| chr2:206759033
|
G | C | 1 | a0002c0002t0002g0147 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.136-1662C>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206759033 | ||||||
| chr2:206759052
|
GGTTT | G | 28 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(25): Show | 54 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.136-1685_136-1682d others(6): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206759052 | ||||||
| chr2:206759114
|
C | T | 7 | a0001c0001t0001g0050a0001c0001t0001g0174a0001c0001t0001g0176others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-1743G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206759114 | ||||||
| chr2:206759263
|
C | T | 1 | a0001c0003t0001g0154 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.135+1638G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206759263 | ||||||
| chr2:206759326
|
G | A | 1 | a0002c0002t0001g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.135+1575C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206759326 | ||||||
| chr2:206759634
|
G | C | 104 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0036others(101): Show | 197 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.135+1267C>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206759634 | ||||||
| chr2:206759634
|
G | T | 2 | a0002c0002t0002g0106a0002c0002t0002g0149 | 2 | NA18981.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.135+1267C>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206759634 | ||||||
| chr2:206759688
|
T | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0038others(63): Show | 131 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.135+1213A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206759688 | ||||||
| chr2:206759709
|
A | T | 1 | a0002c0002t0002g0105 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.135+1192T>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206759709 | ||||||
| chr2:206759764
|
C | T | 1 | a0001c0001t0001g0025 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.135+1137G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206759764 | ||||||
| chr2:206759833
|
A | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0036others(109): Show | 209 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.135+1068T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206759833 | ||||||
| chr2:206759924
|
A | G | 1 | a0002c0002t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.135+977T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206759924 | ||||||
| chr2:206759949
|
T | G | 29 | a0001c0001t0001g0169a0001c0003t0001g0006a0001c0003t0001g0010others(26): Show | 55 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.135+952A>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206759949 | ||||||
| chr2:206760271
|
T | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0099 | 3 | HG00741.hp2 HG01891.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.135+630A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206760271 | ||||||
| chr2:206760333
|
C | T | 1 | a0003c0004t0002g0055 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.135+568G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206760333 | ||||||
| chr2:206760395
|
T | C | 1 | a0002c0002t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.135+506A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206760395 | ||||||
| chr2:206760420
|
G | C | 1 | a0001c0001t0001g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.135+481C>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206760420 | ||||||
| chr2:206760440
|
C | A | 28 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(25): Show | 54 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.135+461G>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206760440 | ||||||
| chr2:206760464
|
A | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0036others(109): Show | 209 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.135+437T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206760464 | ||||||
| chr2:206760692
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.135+209C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206760692 | ||||||
| chr2:206760843
|
T | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0038others(63): Show | 131 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.135+58A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 2/11 | chr2 | 206760843 | ||||||
| chr2:206761406
|
G | A | 28 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(25): Show | 54 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.23-393C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206761406 | ||||||
| chr2:206761413
|
T | C | 2 | a0002c0002t0001g0092a0002c0002t0001g0093 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.23-400A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206761413 | ||||||
| chr2:206761520
|
C | G | 3 | a0001c0001t0001g0036a0001c0001t0001g0090a0001c0001t0001g0091 | 4 | HG01243.hp2 HG02965.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-507G>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206761520 | ||||||
| chr2:206761560
|
A | G | 28 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0003t0001g0023others(25): Show | 54 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.23-547T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206761560 | ||||||
| chr2:206761563
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0038others(91): Show | 185 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.23-550G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206761563 | ||||||
| chr2:206761729
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.23-716T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206761729 | ||||||
| chr2:206761954
|
G | A | 1 | a0001c0003t0001g0048 | 2 | NA18968.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.23-941C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206761954 | ||||||
| chr2:206761982
|
T | C | 10 | a0001c0001t0001g0050a0001c0001t0001g0170a0001c0001t0001g0174others(7): Show | 14 | HG01884.hp1 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.23-969A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206761982 | ||||||
| chr2:206762166
|
T | A | 29 | a0001c0001t0001g0169a0001c0003t0001g0006a0001c0003t0001g0010others(26): Show | 55 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.23-1153A>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206762166 | ||||||
| chr2:206762167
|
C | CA | 29 | a0001c0001t0001g0169a0001c0003t0001g0006a0001c0003t0001g0010others(26): Show | 55 | HG00280.hp2 HG00423.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.23-1155dupT | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206762167 | ||||||
| chr2:206762698
|
C | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0038others(100): Show | 195 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.23-1685G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206762698 | ||||||
| chr2:206762872
|
T | C | 1 | a0002c0002t0002g0149 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.23-1859A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206762872 | ||||||
| chr2:206762938
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.23-1925T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206762938 | ||||||
| chr2:206762952
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.23-1939C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206762952 | ||||||
| chr2:206762964
|
C | T | 1 | a0001c0003t0001g0023 | 3 | HG02559.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.23-1951G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206762964 | ||||||
| chr2:206763044
|
TCTC | T | 2 | a0002c0002t0001g0017a0002c0002t0001g0178 | 5 | HG01069.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.23-2034_23-2032del others(3): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206763044 | ||||||
| chr2:206763070
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.23-2057G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206763070 | ||||||
| chr2:206763230
|
C | A | 1 | a0001c0001t0001g0150 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.22+2020G>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206763230 | ||||||
| chr2:206763241
|
CT | C | 78 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0038others(75): Show | 147 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.22+2008delA | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206763241 | ||||||
| chr2:206763291
|
T | C | 1 | a0002c0002t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.22+1959A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206763291 | ||||||
| chr2:206763337
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.22+1913G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206763337 | ||||||
| chr2:206763357
|
A | G | 2 | a0002c0002t0001g0016a0002c0002t0001g0173 | 5 | HG02258.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.22+1893T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206763357 | ||||||
| chr2:206763388
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.22+1862A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206763388 | ||||||
| chr2:206763394
|
C | G | 1 | a0001c0001t0001g0101 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.22+1856G>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206763394 | ||||||
| chr2:206763459
|
G | C | 1 | a0001c0003t0001g0171 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.22+1791C>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206763459 | ||||||
| chr2:206763489
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.22+1761A>G | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206763489 | ||||||
| chr2:206763571
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.22+1679T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206763571 | ||||||
| chr2:206763654
|
C | T | 1 | a0005c0008t0002g0051 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.22+1596G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206763654 | ||||||
| chr2:206763794
|
G | T | 2 | a0002c0002t0001g0017a0002c0002t0001g0178 | 5 | HG01069.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.22+1456C>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206763794 | ||||||
| chr2:206763899
|
T | TC | 111 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0036others(108): Show | 208 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.22+1350dupG | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206763899 | ||||||
| chr2:206763926
|
GC | G | 3 | a0001c0001t0001g0036a0001c0001t0001g0090a0001c0001t0001g0091 | 4 | HG01243.hp2 HG02965.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+1323delG | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206763926 | ||||||
| chr2:206763942
|
A | T | 1 | a0002c0002t0001g0172 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.22+1308T>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206763942 | ||||||
| chr2:206764159
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.22+1091T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206764159 | ||||||
| chr2:206764212
|
C | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0090a0001c0001t0001g0091 | 4 | HG01243.hp2 HG02965.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+1038G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206764212 | ||||||
| chr2:206764277
|
G | A | 7 | a0001c0001t0001g0050a0001c0001t0001g0174a0001c0001t0001g0176others(4): Show | 11 | HG01884.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.22+973C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206764277 | ||||||
| chr2:206764297
|
C | CA | 70 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0041others(67): Show | 135 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.22+952dupT | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206764297 | ||||||
| chr2:206764578
|
C | T | 1 | a0002c0006t0001g0153 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.22+672G>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206764578 | ||||||
| chr2:206764638
|
C | A | 2 | a0002c0002t0001g0017a0002c0002t0001g0178 | 5 | HG01069.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.22+612G>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206764638 | ||||||
| chr2:206764828
|
C | G | 1 | a0002c0002t0001g0152 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.22+422G>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206764828 | ||||||
| chr2:206764901
|
A | G | 1 | a0009c0014t0001g0151 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.22+349T>C | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206764901 | ||||||
| chr2:206765071
|
T | A | 70 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0038others(67): Show | 135 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.22+179A>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206765071 | ||||||
| chr2:206765097
|
T | TGCAA | 75 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0036others(72): Show | 141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.22+152_22+153insTT others(2): Show |
MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206765097 | ||||||
| chr2:206765122
|
A | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0036others(72): Show | 141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.22+128T>A | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206765122 | ||||||
| chr2:206765180
|
G | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0036others(113): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.22+70C>T | MDH1B | ENSG00000138400.13 | transcript | ENST00000374412.8 | protein_coding | 1/11 | chr2 | 206765180 |