Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4191 |
| ensemblid | ENSG00000146701.12 |
| hgncid | 6971 |
| symbol | MDH2 |
| name | malate dehydrogenase 2 |
| refseq_nuc | NM_005918.4 |
| refseq_prot | NP_005909.2 |
| ensembl_nuc | ENST00000315758.10 |
| ensembl_prot | ENSP00000327070.5 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 76048106 |
| end | 76067508 |
| strand | + |
| ver | v1.2 |
| region | chr7:76048106-76067508 |
| region5000 | chr7:76043106-76072508 |
| regionname0 | MDH2_chr7_76048106_76067508 |
| regionname5000 | MDH2_chr7_76043106_76072508 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 338 | 235 | 61 | 28 | 115 | 6 | 25 | 95 | MDH2_chr7_76043106_76072508 | MDH2 | MLSAL others(333): Show |
chr7 | 76043106 | 76072508 |
| a0002 | 1/1 | 338 | 151 | 23 | 35 | 61 | 10 | 20 | 47 | MDH2_chr7_76043106_76072508 | MDH2 | MLSAL others(333): Show |
chr7 | 76043106 | 76072508 |
| a0003 | 0/0 | 338 | 9 | 1 | 7 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | MLSAL others(333): Show |
chr7 | 76043106 | 76072508 |
| a0004 | 0/0 | 338 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | MLSAL others(333): Show |
chr7 | 76043106 | 76072508 |
| a0005 | 0/0 | 338 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | MLSAL others(333): Show |
chr7 | 76043106 | 76072508 |
| a0006 | 0/0 | 338 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | MLSAL others(333): Show |
chr7 | 76043106 | 76072508 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1014 | 229 | 57 | 26 | 115 | 6 | 25 | MDH2_chr7_76043106_76072508 | MDH2 | ATGCT others(1009): Show |
chr7 | 76043106 | 76072508 | ||
| a0001c0004 | 0/0 | 1014 | 4 | 3 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ATGCT others(1009): Show |
chr7 | 76043106 | 76072508 | ||
| a0001c0008 | 0/0 | 1014 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ATGCT others(1009): Show |
chr7 | 76043106 | 76072508 | ||
| a0001c0010 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ATGCT others(1009): Show |
chr7 | 76043106 | 76072508 | ||
| a0002c0002 | 1/1 | 1014 | 147 | 19 | 35 | 61 | 10 | 20 | MDH2_chr7_76043106_76072508 | MDH2 | ATGCT others(1009): Show |
chr7 | 76043106 | 76072508 | ||
| a0002c0005 | 0/0 | 1014 | 2 | 2 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ATGCT others(1009): Show |
chr7 | 76043106 | 76072508 | ||
| a0002c0006 | 0/0 | 1014 | 2 | 2 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ATGCT others(1009): Show |
chr7 | 76043106 | 76072508 | ||
| a0003c0003 | 0/0 | 1014 | 9 | 1 | 7 | 0 | 1 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ATGCT others(1009): Show |
chr7 | 76043106 | 76072508 | ||
| a0004c0007 | 0/0 | 1014 | 1 | 0 | 0 | 0 | 1 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ATGCT others(1009): Show |
chr7 | 76043106 | 76072508 | ||
| a0005c0009 | 0/0 | 1014 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | ATGCT others(1009): Show |
chr7 | 76043106 | 76072508 | ||
| a0006c0011 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ATGCT others(1009): Show |
chr7 | 76043106 | 76072508 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2170 | 147 | 19 | 16 | 84 | 5 | 23 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| a0001c0001t0002 | 0/0 | 2170 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| a0001c0001t0003 | 0/0 | 2170 | 71 | 29 | 8 | 31 | 1 | 2 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| a0001c0001t0005 | 0/0 | 2170 | 5 | 5 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| a0001c0001t0007 | 0/0 | 2170 | 2 | 2 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| a0001c0001t0009 | 0/0 | 2170 | 2 | 2 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| a0001c0001t0011 | 0/0 | 2170 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| a0001c0004t0001 | 0/0 | 2170 | 4 | 3 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| a0001c0008t0001 | 0/0 | 2170 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| a0001c0010t0003 | 0/0 | 2170 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| a0002c0002t0002 | 0/1 | 2170 | 138 | 12 | 35 | 60 | 10 | 20 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| a0002c0002t0003 | 0/0 | 2170 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| a0002c0002t0004 | 0/0 | 2170 | 6 | 6 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| a0002c0002t0006 | 0/0 | 2170 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| a0002c0002t0010 | 1/0 | 2170 | 1 | 0 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| a0002c0005t0008 | 0/0 | 2170 | 2 | 2 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| a0002c0006t0006 | 0/0 | 2170 | 2 | 2 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| a0003c0003t0002 | 0/0 | 2170 | 9 | 1 | 7 | 0 | 1 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| a0004c0007t0002 | 0/0 | 2170 | 1 | 0 | 0 | 0 | 1 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| a0005c0009t0001 | 0/0 | 2170 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| a0006c0011t0001 | 0/0 | 2170 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | ACTTC others(2165): Show |
chr7 | 76043106 | 76072508 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 31 | 1 | 3 | 19 | 3 | 5 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0003 | 0/0 | 14 | 0 | 4 | 10 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0009 | 0/0 | 7 | 2 | 0 | 0 | 0 | 5 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0010 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0025 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0026 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0005 | 0/0 | 11 | 1 | 3 | 6 | 1 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0007 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0012 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0020 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0005g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0009g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0001t0011g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0004t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0004t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0004t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0008t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0001c0010t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0001 | 0/0 | 33 | 0 | 9 | 16 | 1 | 7 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0004 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0006 | 0/0 | 11 | 0 | 4 | 5 | 2 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0008 | 0/0 | 8 | 0 | 4 | 2 | 0 | 2 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0011 | 0/0 | 6 | 3 | 3 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0016 | 0/0 | 4 | 0 | 0 | 0 | 3 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0018 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0029 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0046 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0047 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0156 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0004g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0002t0010g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0005t0008g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0005t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0002c0006t0006g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0003c0003t0002g0004 | 0/0 | 8 | 1 | 6 | 0 | 1 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0003c0003t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0004c0007t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0005c0009t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| a0006c0011t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | GBR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0137 | EUR | GBR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0005 | EUR | FIN | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00323 | hp1 | a0004 | c0007 | t0002 | g0001 | EUR | FIN | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0045 | EAS | CHS | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | CHS | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0130 | EAS | CHS | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00738 | hp2 | a0003 | c0003 | t0002 | g0004 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00741 | hp1 | a0003 | c0003 | t0002 | g0004 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0140 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0125 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0047 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0011 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0145 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01099 | hp2 | a0003 | c0003 | t0002 | g0004 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01106 | hp1 | a0001 | c0001 | t0011 | g0116 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0046 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0154 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01168 | hp2 | a0003 | c0003 | t0002 | g0004 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01169 | hp2 | a0003 | c0003 | t0002 | g0004 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01175 | hp1 | a0003 | c0003 | t0002 | g0060 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PUR | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01255 | hp1 | a0003 | c0003 | t0002 | g0004 | AMR | CLM | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0055 | AMR | CLM | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0134 | AMR | CLM | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0044 | AMR | CLM | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0044 | AMR | CLM | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | CLM | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0136 | AMR | CLM | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0153 | AMR | CLM | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01433 | hp1 | a0001 | c0004 | t0001 | g0104 | AMR | CLM | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | CLM | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0016 | EUR | IBS | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0138 | EUR | IBS | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01516 | hp1 | a0003 | c0003 | t0002 | g0004 | EUR | IBS | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0030 | EUR | IBS | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0030 | EUR | IBS | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0016 | EUR | IBS | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | ACB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | ACB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0056 | AMR | PEL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | PEL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | PEL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | KHV | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0050 | EAS | KHV | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0064 | AFR | ACB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | KHV | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | KHV | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | KHV | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0128 | EAS | KHV | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0131 | EAS | KHV | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | KHV | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | KHV | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | ACB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0152 | AMR | PEL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02257 | hp2 | a0002 | c0005 | t0008 | g0059 | AFR | ACB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | ACB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02258 | hp2 | a0002 | c0002 | t0004 | g0024 | AFR | ACB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02273 | hp2 | a0001 | c0008 | t0001 | g0189 | AMR | PEL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | ACB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0004 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02622 | hp1 | a0002 | c0006 | t0006 | g0032 | AFR | GWD | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02630 | hp1 | a0002 | c0006 | t0006 | g0032 | AFR | GWD | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02630 | hp2 | a0001 | c0004 | t0001 | g0041 | AFR | GWD | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0008 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0062 | AFR | GWD | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0155 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0065 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02809 | hp1 | a0001 | c0010 | t0003 | g0084 | AFR | GWD | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0066 | AFR | GWD | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02895 | hp1 | a0002 | c0002 | t0004 | g0164 | AFR | GWD | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | ESN | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0052 | AFR | ESN | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0103 | AFR | ESN | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02970 | hp2 | a0001 | c0004 | t0001 | g0041 | AFR | ESN | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | ESN | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03017 | hp1 | a0005 | c0009 | t0001 | g0180 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0008 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0142 | AFR | MSL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0031 | AFR | MSL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03130 | hp1 | a0002 | c0002 | t0004 | g0166 | AFR | ESN | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | ESN | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03139 | hp1 | a0002 | c0002 | t0004 | g0024 | AFR | ESN | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | ESN | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | ESN | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0052 | AFR | MSL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03225 | hp1 | a0002 | c0002 | t0006 | g0068 | AFR | MSL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03453 | hp1 | a0001 | c0004 | t0001 | g0105 | AFR | MSL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0031 | AFR | MSL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03486 | hp1 | a0002 | c0005 | t0008 | g0058 | AFR | MSL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0016 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0029 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | ESN | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | ESN | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0107 | AFR | MSL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0143 | AFR | MSL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0122 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0133 | SAS | STU | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0061 | SAS | STU | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0018 | SAS | BEB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | BEB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0139 | SAS | BEB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0057 | SAS | STU | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | STU | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | STU | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0067 | SAS | STU | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0121 | SAS | STU | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | STU | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | YRI | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | YRI | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | CHB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | CHB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | CHB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | YRI | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18906 | hp2 | a0002 | c0002 | t0004 | g0024 | AFR | YRI | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18961 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0106 | AFR | LWK | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | LWK | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0072 | AFR | LWK | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | LWK | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19070 | hp1 | a0002 | c0002 | t0003 | g0135 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | YRI | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | YRI | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | ASW | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ASW | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0001 | EUR | TSI | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0006 | EUR | TSI | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0006 | EUR | TSI | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0016 | EUR | TSI | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | GIH | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0157 | AFR | ACB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02486 | hp1 | a0002 | c0002 | t0004 | g0167 | AFR | ACB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | ACB | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | USA | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | USA | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0158 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | USA | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA20300 | hp2 | a0006 | c0011 | t0001 | g0182 | AFR | USA | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | LWK | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| NA21309 | hp2 | a0003 | c0003 | t0002 | g0004 | AFR | LWK | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0156 | REF | REF | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0010 | g0165 | REF | REF | MDH2_chr7_76043106_76072508 | MDH2 | chr7 | 76043106 | 76072508 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:76048186 | C | T | 3 | a0001 a0005 a0006 |
237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
missense_variant | MODERATE | c.26C>T | p.Ala9Val | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/9 | 81/2170 | 26/1017 | 9/338 | chr7 | 76048186 | |||
| chr7:76058064 | G | A | 1 | a0004 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.415G>A | p.Val139Ile | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/9 | 470/2170 | 415/1017 | 139/338 | chr7 | 76058064 | |||
| chr7:76063539 | G | A | 1 | a0005 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.580G>A | p.Val194Ile | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 6/9 | 635/2170 | 580/1017 | 194/338 | chr7 | 76063539 | |||
| chr7:76064390 | C | G | 1 | a0006 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.685C>G | p.Arg229Gly | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 7/9 | 740/2170 | 685/1017 | 229/338 | chr7 | 76064390 | |||
| chr7:76066295 | A | G | 1 | a0003 | 9 | HG00738.hp2 HG00741.hp1 HG01099.hp2 others(6): Show |
missense_variant | MODERATE | c.902A>G | p.Lys301Arg | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 9/9 | 957/2170 | 902/1017 | 301/338 | chr7 | 76066295 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:76054901 | C | T | 1 | a0001c0004 | 4 | HG01433.hp1 HG02630.hp2 HG02970.hp2 others(1): Show |
synonymous_variant | LOW | c.138C>T | p.Asn46Asn | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/9 | 193/2170 | 138/1017 | 46/338 | chr7 | 76054901 | |||
| chr7:76054955 | G | A | 1 | a0002c0005 | 2 | HG02257.hp2 HG03486.hp1 |
synonymous_variant | LOW | c.192G>A | p.Val64Val | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/9 | 247/2170 | 192/1017 | 64/338 | chr7 | 76054955 | |||
| chr7:76058078 | G | A | 1 | a0001c0008 | 1 | HG02273.hp2 | splice_region_variant&synonymous_variant | LOW | c.429G>A | p.Pro143Pro | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/9 | 484/2170 | 429/1017 | 143/338 | chr7 | 76058078 | |||
| chr7:76060498 | G | A | 1 | a0002c0006 | 2 | HG02622.hp1 HG02630.hp1 |
splice_region_variant&synonymous_variant | LOW | c.555G>A | p.Lys185Lys | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/9 | 610/2170 | 555/1017 | 185/338 | chr7 | 76060498 | |||
| chr7:76066392 | C | T | 1 | a0001c0010 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.999C>T | p.Phe333Phe | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 9/9 | 1054/2170 | 999/1017 | 333/338 | chr7 | 76066392 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:76048112 | C | G | 17 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(14): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
5_prime_UTR_variant | MODIFIER | c.-49C>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/9 | 49 | chr7 | 76048112 | ||||||
| chr7:76066590 | A | G | 3 | a0001c0001t0003 a0001c0010t0003 a0002c0002t0003 |
73 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*180A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 9/9 | 180 | chr7 | 76066590 | ||||||
| chr7:76066671 | C | T | 3 | a0002c0002t0004 a0002c0002t0006 a0002c0006t0006 |
9 | HG02258.hp2 HG02486.hp1 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*261C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 9/9 | 261 | chr7 | 76066671 | ||||||
| chr7:76066786 | C | T | 1 | a0001c0001t0005 | 5 | HG02559.hp2 HG02976.hp1 HG03195.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*376C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 9/9 | 376 | chr7 | 76066786 | ||||||
| chr7:76066828 | G | A | 2 | a0001c0001t0005 a0001c0001t0007 |
7 | HG02559.hp2 HG02970.hp1 HG02976.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*418G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 9/9 | 418 | chr7 | 76066828 | ||||||
| chr7:76066870 | T | G | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(12): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
3_prime_UTR_variant | MODIFIER | c.*460T>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 9/9 | 460 | chr7 | 76066870 | ||||||
| chr7:76066882 | C | T | 1 | a0001c0001t0009 | 2 | HG02922.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*472C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 9/9 | 472 | chr7 | 76066882 | ||||||
| chr7:76067102 | A | G | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(12): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*692A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 9/9 | 692 | chr7 | 76067102 | ||||||
| chr7:76067281 | T | C | 1 | a0002c0002t0004 | 6 | HG02258.hp2 HG02486.hp1 HG02895.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*871T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 9/9 | 871 | chr7 | 76067281 | ||||||
| chr7:76067288 | G | C | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(12): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*878G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 9/9 | 878 | chr7 | 76067288 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:76048260 | G | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(31): Show |
86 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.66+34G>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76048260 | |||||||
| chr7:76048261 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.66+35C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76048261 | |||||||
| chr7:76048421 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(31): Show |
86 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.66+195G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76048421 | |||||||
| chr7:76048486 | T | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(184): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.66+260T>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76048486 | |||||||
| chr7:76048537 | G | A | 2 | a0001c0001t0001g0168 a0002c0002t0002g0055 |
2 | HG01255.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.66+311G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76048537 | |||||||
| chr7:76048624 | T | C | 1 | a0002c0002t0002g0056 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.66+398T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76048624 | |||||||
| chr7:76048710 | A | C | 4 | a0001c0001t0001g0051 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
5 | HG04199.hp1 HG04204.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+484A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76048710 | |||||||
| chr7:76048981 | CGGGGGG | C | 32 | a0001c0001t0002g0190 a0001c0001t0003g0017 a0001c0001t0003g0144 others(29): Show |
64 | HG00099.hp2 HG00423.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.66+767_66+772delGG others(4): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 76048981 | ||||||
| chr7:76048981 | CGGGGGGG | C | 22 | a0001c0001t0001g0163 a0002c0002t0002g0001 a0002c0002t0002g0018 others(19): Show |
64 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.66+766_66+772delGG others(5): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 76048981 | ||||||
| chr7:76048981 | CGGGGGGG others(4): Show |
C | 1 | a0001c0001t0001g0160 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.66+762_66+772delGG others(9): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 76048981 | ||||||
| chr7:76048983 | G | GGGGGT | 28 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(25): Show |
43 | HG00140.hp1 HG01975.hp1 HG02080.hp1 others(40): Show |
intron_variant | MODIFIER | c.66+761_66+762insTG others(3): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 76048983 | ||||||
| chr7:76048983 | G | GGGGGTGG others(6): Show |
1 | a0001c0001t0001g0161 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.66+761_66+762insTG others(11): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 76048983 | ||||||
| chr7:76048984 | G | GGGGT | 28 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(25): Show |
51 | HG00280.hp1 HG00609.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.66+761_66+762insTG others(2): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 76048984 | ||||||
| chr7:76048984 | G | GGGGTGGG others(6): Show |
1 | a0001c0001t0001g0051 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.66+761_66+762insTG others(11): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 76048984 | ||||||
| chr7:76048985 | G | GGGT | 17 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(14): Show |
25 | HG00323.hp2 HG00423.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.66+761_66+762insTG others(1): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 76048985 | ||||||
| chr7:76048985 | G | GGGTGGGG others(4): Show |
2 | a0001c0001t0001g0051 a0001c0001t0001g0162 |
2 | HG04199.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.66+761_66+762insTG others(9): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 76048985 | ||||||
| chr7:76048990 | G | T | 1 | a0001c0001t0003g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.66+764G>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76048990 | |||||||
| chr7:76049034 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.66+808A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76049034 | |||||||
| chr7:76049325 | T | C | 1 | a0001c0001t0001g0028 | 2 | NA18992.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.66+1099T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76049325 | |||||||
| chr7:76049326 | G | A | 70 | a0001c0001t0002g0190 a0002c0002t0002g0001 a0002c0002t0002g0004 others(67): Show |
154 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.66+1100G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76049326 | |||||||
| chr7:76049417 | G | A | 68 | a0001c0001t0002g0190 a0002c0002t0002g0001 a0002c0002t0002g0004 others(65): Show |
151 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.66+1191G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76049417 | |||||||
| chr7:76049611 | A | T | 2 | a0002c0002t0006g0068 a0002c0006t0006g0032 |
3 | HG02622.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.66+1385A>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76049611 | |||||||
| chr7:76049684 | G | T | 2 | a0001c0001t0003g0121 a0001c0001t0003g0122 |
2 | HG03654.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.66+1458G>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76049684 | |||||||
| chr7:76049781 | A | G | 17 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0043 others(14): Show |
25 | HG00099.hp1 HG00140.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.66+1555A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76049781 | |||||||
| chr7:76049863 | C | T | 1 | a0002c0002t0002g0067 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.66+1637C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76049863 | |||||||
| chr7:76049944 | G | A | 1 | a0002c0002t0002g0057 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.66+1718G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76049944 | |||||||
| chr7:76049978 | C | T | 2 | a0001c0001t0005g0015 a0001c0001t0005g0107 |
5 | HG02559.hp2 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.66+1752C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76049978 | |||||||
| chr7:76050050 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.66+1824C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76050050 | |||||||
| chr7:76050066 | CTG | C | 7 | a0001c0001t0005g0015 a0001c0001t0005g0107 a0001c0001t0007g0103 others(4): Show |
11 | HG01433.hp1 HG02559.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.66+1842_66+1843del others(2): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 76050066 | ||||||
| chr7:76050088 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.66+1862G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76050088 | |||||||
| chr7:76050174 | C | G | 2 | a0002c0002t0002g0142 a0002c0002t0002g0143 |
2 | HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.66+1948C>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76050174 | |||||||
| chr7:76050184 | G | A | 2 | a0001c0001t0003g0070 a0002c0002t0006g0068 |
2 | HG03225.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.66+1958G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76050184 | |||||||
| chr7:76050413 | A | C | 1 | a0002c0002t0002g0066 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.66+2187A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76050413 | |||||||
| chr7:76050508 | A | T | 1 | a0002c0002t0002g0067 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.66+2282A>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76050508 | |||||||
| chr7:76050708 | G | A | 68 | a0001c0001t0002g0190 a0002c0002t0002g0001 a0002c0002t0002g0004 others(65): Show |
151 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.66+2482G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76050708 | |||||||
| chr7:76050843 | T | C | 1 | a0002c0006t0006g0032 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.66+2617T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76050843 | |||||||
| chr7:76050913 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0071 |
5 | HG00609.hp2 HG02129.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+2687G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76050913 | |||||||
| chr7:76050942 | C | T | 2 | a0002c0002t0006g0068 a0002c0006t0006g0032 |
3 | HG02622.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.66+2716C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76050942 | |||||||
| chr7:76050951 | G | A | 1 | a0001c0001t0003g0072 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.66+2725G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76050951 | |||||||
| chr7:76050967 | C | G | 1 | a0001c0008t0001g0189 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.66+2741C>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76050967 | |||||||
| chr7:76051083 | C | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
5 | HG04199.hp1 HG04204.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+2857C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76051083 | |||||||
| chr7:76051154 | G | C | 1 | a0001c0001t0001g0073 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.66+2928G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76051154 | |||||||
| chr7:76051181 | G | A | 2 | a0002c0002t0006g0068 a0002c0006t0006g0032 |
3 | HG02622.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.66+2955G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76051181 | |||||||
| chr7:76051200 | C | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(184): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.66+2974C>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76051200 | |||||||
| chr7:76051224 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.66+2998T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76051224 | |||||||
| chr7:76051237 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0119 |
3 | HG00099.hp1 HG01358.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.66+3011C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76051237 | |||||||
| chr7:76051318 | A | AT | 43 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(40): Show |
72 | HG00609.hp2 HG00621.hp1 HG01106.hp1 others(69): Show |
intron_variant | MODIFIER | c.66+3112dupT | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 76051318 | ||||||
| chr7:76051318 | AT | A | 38 | a0001c0001t0001g0170 a0001c0001t0003g0005 a0001c0001t0003g0007 others(35): Show |
73 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.66+3112delT | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 76051318 | ||||||
| chr7:76051332 | T | TTTTTTTG others(85): Show |
1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.66+3107_66+3198dup others(92): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 76051332 | ||||||
| chr7:76051351 | C | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(29): Show |
83 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.66+3125C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76051351 | |||||||
| chr7:76051357 | T | C | 32 | a0002c0002t0002g0001 a0002c0002t0002g0008 a0002c0002t0002g0018 others(29): Show |
82 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.66+3131T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76051357 | |||||||
| chr7:76051385 | G | A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(29): Show |
83 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.66+3159G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76051385 | |||||||
| chr7:76051447 | G | A | 1 | a0001c0001t0003g0074 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.66+3221G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76051447 | |||||||
| chr7:76051503 | T | G | 1 | a0002c0002t0002g0126 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.66+3277T>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76051503 | |||||||
| chr7:76051564 | G | A | 2 | a0002c0005t0008g0058 a0002c0005t0008g0059 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.67-3266G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76051564 | |||||||
| chr7:76051589 | A | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(183): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.67-3241A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76051589 | |||||||
| chr7:76051598 | C | T | 58 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0028 others(55): Show |
112 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.67-3232C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76051598 | |||||||
| chr7:76051647 | C | A | 1 | a0002c0002t0002g0044 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.67-3183C>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76051647 | |||||||
| chr7:76051681 | T | C | 1 | a0001c0001t0003g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.67-3149T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76051681 | |||||||
| chr7:76051749 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.67-3081C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76051749 | |||||||
| chr7:76051776 | G | A | 66 | a0001c0001t0002g0190 a0002c0002t0002g0001 a0002c0002t0002g0004 others(63): Show |
149 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.67-3054G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76051776 | |||||||
| chr7:76051888 | A | G | 4 | a0001c0001t0001g0051 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
5 | HG04199.hp1 HG04204.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-2942A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76051888 | |||||||
| chr7:76052111 | G | A | 1 | a0002c0002t0006g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.67-2719G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76052111 | |||||||
| chr7:76052111 | G | T | 1 | a0002c0002t0002g0125 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.67-2719G>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76052111 | |||||||
| chr7:76052132 | C | G | 73 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(70): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.67-2698C>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76052132 | |||||||
| chr7:76052193 | T | G | 3 | a0001c0001t0003g0007 a0001c0001t0003g0076 a0001c0001t0003g0077 |
11 | HG00639.hp1 HG01192.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.67-2637T>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76052193 | |||||||
| chr7:76052354 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.67-2476C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76052354 | |||||||
| chr7:76052430 | C | CA | 64 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(61): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.67-2379dupA | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 76052430 | ||||||
| chr7:76052430 | C | CAA | 41 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0028 others(38): Show |
69 | HG00140.hp2 HG00609.hp2 HG01175.hp2 others(66): Show |
intron_variant | MODIFIER | c.67-2380_67-2379dup others(2): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 76052430 | ||||||
| chr7:76052430 | C | CAAA | 6 | a0001c0001t0001g0039 a0001c0001t0001g0089 a0001c0001t0001g0101 others(3): Show |
7 | HG01433.hp1 HG01934.hp2 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.67-2381_67-2379dup others(3): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 76052430 | ||||||
| chr7:76052430 | CAAAAAAA others(1): Show |
C | 66 | a0001c0001t0002g0190 a0002c0002t0002g0001 a0002c0002t0002g0004 others(63): Show |
149 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.67-2386_67-2379del others(8): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 76052430 | ||||||
| chr7:76052470 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.67-2360G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76052470 | |||||||
| chr7:76052480 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0169 |
3 | HG03209.hp2 NA18992.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.67-2350C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76052480 | |||||||
| chr7:76052562 | A | AT | 22 | a0001c0001t0001g0054 a0001c0001t0001g0091 a0001c0001t0001g0099 others(19): Show |
30 | HG00621.hp2 HG00673.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.67-2249dupT | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 76052562 | ||||||
| chr7:76052562 | AT | A | 11 | a0001c0001t0003g0034 a0001c0001t0003g0088 a0001c0001t0003g0092 others(8): Show |
14 | HG00423.hp1 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-2249delT | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 76052562 | ||||||
| chr7:76052823 | T | A | 1 | a0002c0002t0002g0030 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.67-2007T>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76052823 | |||||||
| chr7:76052918 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.67-1912C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76052918 | |||||||
| chr7:76052988 | C | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(81): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.67-1842C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76052988 | |||||||
| chr7:76053012 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0184 a0001c0001t0007g0106 |
7 | NA18747.hp2 NA18945.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-1818C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76053012 | |||||||
| chr7:76053075 | C | G | 1 | a0002c0002t0004g0166 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.67-1755C>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76053075 | |||||||
| chr7:76053189 | A | T | 1 | a0002c0002t0002g0139 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.67-1641A>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76053189 | |||||||
| chr7:76053288 | C | A | 4 | a0002c0002t0004g0024 a0002c0002t0004g0164 a0002c0002t0004g0166 others(1): Show |
6 | HG02258.hp2 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-1542C>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76053288 | |||||||
| chr7:76053313 | A | G | 1 | a0001c0001t0003g0086 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.67-1517A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76053313 | |||||||
| chr7:76053508 | T | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0028 others(55): Show |
112 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.67-1322T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76053508 | |||||||
| chr7:76053565 | C | T | 62 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0028 others(59): Show |
118 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.67-1265C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76053565 | |||||||
| chr7:76053591 | G | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(78): Show |
146 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.67-1239G>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76053591 | |||||||
| chr7:76053670 | G | C | 8 | a0001c0001t0003g0007 a0001c0001t0003g0021 a0001c0001t0003g0034 others(5): Show |
19 | HG00639.hp1 HG01192.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.67-1160G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76053670 | |||||||
| chr7:76053671 | C | T | 8 | a0001c0001t0003g0007 a0001c0001t0003g0021 a0001c0001t0003g0034 others(5): Show |
19 | HG00639.hp1 HG01192.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.67-1159C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76053671 | |||||||
| chr7:76053689 | G | A | 4 | a0001c0001t0001g0051 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
5 | HG04199.hp1 HG04204.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-1141G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76053689 | |||||||
| chr7:76053742 | G | GCTGCCTG others(1): Show |
3 | a0001c0001t0003g0085 a0001c0001t0003g0093 a0001c0010t0003g0084 |
3 | HG02809.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.67-1074_67-1067dup others(8): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 76053742 | ||||||
| chr7:76053763 | C | T | 3 | a0001c0004t0001g0041 a0001c0004t0001g0104 a0001c0004t0001g0105 |
4 | HG01433.hp1 HG02630.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-1067C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76053763 | |||||||
| chr7:76053813 | C | T | 1 | a0001c0008t0001g0189 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.67-1017C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76053813 | |||||||
| chr7:76053862 | G | C | 1 | a0001c0001t0003g0080 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.67-968G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76053862 | |||||||
| chr7:76054084 | G | A | 3 | a0002c0002t0002g0016 a0002c0002t0002g0029 a0002c0002t0002g0044 |
8 | HG01257.hp1 HG01258.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.67-746G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76054084 | |||||||
| chr7:76054179 | C | G | 4 | a0002c0002t0004g0024 a0002c0002t0004g0164 a0002c0002t0004g0166 others(1): Show |
6 | HG02258.hp2 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-651C>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76054179 | |||||||
| chr7:76054225 | C | T | 4 | a0002c0002t0004g0024 a0002c0002t0004g0164 a0002c0002t0004g0166 others(1): Show |
6 | HG02258.hp2 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-605C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76054225 | |||||||
| chr7:76054230 | G | A | 3 | a0001c0004t0001g0041 a0001c0004t0001g0104 a0001c0004t0001g0105 |
4 | HG01433.hp1 HG02630.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-600G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76054230 | |||||||
| chr7:76054246 | CTT | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(29): Show |
83 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.67-583_67-582delTT | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76054246 | |||||||
| chr7:76054263 | T | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(116): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.67-567T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76054263 | |||||||
| chr7:76054551 | C | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0028 others(16): Show |
38 | HG00609.hp2 HG01934.hp2 HG01943.hp1 others(35): Show |
intron_variant | MODIFIER | c.67-279C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76054551 | |||||||
| chr7:76054618 | A | C | 2 | a0002c0002t0006g0068 a0002c0006t0006g0032 |
3 | HG02622.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.67-212A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76054618 | |||||||
| chr7:76054705 | C | A | 1 | a0001c0001t0003g0121 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-125C>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76054705 | |||||||
| chr7:76054707 | A | G | 1 | a0002c0002t0002g0031 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.67-123A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76054707 | |||||||
| chr7:76054803 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.67-27G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 1/8 | chr7 | 76054803 | |||||||
| chr7:76055007 | C | T | 1 | a0001c0001t0003g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.235+9C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055007 | |||||||
| chr7:76055008 | G | A | 17 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0043 others(14): Show |
25 | HG00099.hp1 HG00140.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.235+10G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055008 | |||||||
| chr7:76055028 | C | T | 4 | a0002c0002t0004g0024 a0002c0002t0004g0164 a0002c0002t0004g0166 others(1): Show |
6 | HG02258.hp2 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+30C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055028 | |||||||
| chr7:76055059 | T | C | 2 | a0002c0005t0008g0058 a0002c0005t0008g0059 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.235+61T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055059 | |||||||
| chr7:76055081 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+83A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055081 | |||||||
| chr7:76055082 | A | T | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+84A>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055082 | |||||||
| chr7:76055083 | C | T | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+85C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055083 | |||||||
| chr7:76055085 | A | T | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+87A>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055085 | |||||||
| chr7:76055088 | T | A | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+90T>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055088 | |||||||
| chr7:76055096 | G | A | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+98G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055096 | |||||||
| chr7:76055097 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+99A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055097 | |||||||
| chr7:76055098 | C | G | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+100C>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055098 | |||||||
| chr7:76055116 | A | G | 1 | a0001c0001t0003g0036 | 2 | HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.235+118A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055116 | |||||||
| chr7:76055176 | A | T | 1 | a0002c0002t0002g0155 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.235+178A>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055176 | |||||||
| chr7:76055389 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+391A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055389 | |||||||
| chr7:76055530 | G | C | 4 | a0001c0001t0001g0051 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
5 | HG04199.hp1 HG04204.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.235+532G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055530 | |||||||
| chr7:76055589 | T | C | 6 | a0002c0002t0004g0024 a0002c0002t0004g0164 a0002c0002t0004g0166 others(3): Show |
9 | HG02258.hp2 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.235+591T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055589 | |||||||
| chr7:76055604 | G | C | 1 | a0002c0002t0002g0128 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.235+606G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055604 | |||||||
| chr7:76055628 | T | G | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+630T>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055628 | |||||||
| chr7:76055729 | A | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(122): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.235+731A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055729 | |||||||
| chr7:76055737 | C | CA | 19 | a0001c0001t0001g0025 a0001c0001t0001g0095 a0001c0001t0001g0115 others(16): Show |
23 | HG01106.hp1 HG01106.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.235+756dupA | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 76055737 | ||||||
| chr7:76055737 | CAAA | C | 6 | a0002c0002t0004g0024 a0002c0002t0004g0164 a0002c0002t0004g0166 others(3): Show |
9 | HG02258.hp2 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.235+754_235+756del others(3): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 76055737 | ||||||
| chr7:76055754 | A | T | 1 | a0002c0002t0002g0138 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.235+756A>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055754 | |||||||
| chr7:76055822 | GTCACCAA others(17): Show |
G | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+825_235+848del others(24): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055822 | |||||||
| chr7:76055830 | A | AT | 93 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(90): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.235+848dupT | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 76055830 | ||||||
| chr7:76055830 | A | ATT | 29 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(26): Show |
46 | HG00609.hp2 HG01106.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.235+847_235+848dup others(2): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 76055830 | ||||||
| chr7:76055847 | G | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+849G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055847 | |||||||
| chr7:76055860 | C | T | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+862C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055860 | |||||||
| chr7:76055900 | T | A | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+902T>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055900 | |||||||
| chr7:76055961 | G | A | 1 | a0002c0002t0004g0164 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.235+963G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76055961 | |||||||
| chr7:76056003 | T | G | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1005T>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056003 | |||||||
| chr7:76056007 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1009T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056007 | |||||||
| chr7:76056009 | G | A | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1011G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056009 | |||||||
| chr7:76056010 | T | G | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1012T>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056010 | |||||||
| chr7:76056012 | G | T | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1014G>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056012 | |||||||
| chr7:76056020 | G | T | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1022G>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056020 | |||||||
| chr7:76056022 | T | TCCCCCCC others(37): Show |
1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1024_235+1025i others(46): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056022 | |||||||
| chr7:76056052 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1054T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056052 | |||||||
| chr7:76056055 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1057T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056055 | |||||||
| chr7:76056056 | G | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1058G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056056 | |||||||
| chr7:76056057 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1059A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056057 | |||||||
| chr7:76056060 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1062T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056060 | |||||||
| chr7:76056062 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1064A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056062 | |||||||
| chr7:76056063 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1065A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056063 | |||||||
| chr7:76056064 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1066A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056064 | |||||||
| chr7:76056065 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1067T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056065 | |||||||
| chr7:76056066 | G | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1068G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056066 | |||||||
| chr7:76056067 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1069A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056067 | |||||||
| chr7:76056068 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1070T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056068 | |||||||
| chr7:76056071 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1073A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056071 | |||||||
| chr7:76056074 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1076T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056074 | |||||||
| chr7:76056075 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1077A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056075 | |||||||
| chr7:76056078 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1080T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056078 | |||||||
| chr7:76056080 | G | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1082G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056080 | |||||||
| chr7:76056081 | G | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1083G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056081 | |||||||
| chr7:76056083 | C | T | 4 | a0002c0002t0004g0024 a0002c0002t0004g0164 a0002c0002t0004g0166 others(1): Show |
6 | HG02258.hp2 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+1085C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056083 | |||||||
| chr7:76056084 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1086T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056084 | |||||||
| chr7:76056087 | CAAAGTGC others(6): Show |
C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1090_235+1102d others(15): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056087 | |||||||
| chr7:76056101 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1103T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056101 | |||||||
| chr7:76056102 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1104A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056102 | |||||||
| chr7:76056104 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1106A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056104 | |||||||
| chr7:76056105 | G | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1107G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056105 | |||||||
| chr7:76056106 | G | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1108G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056106 | |||||||
| chr7:76056108 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1110A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056108 | |||||||
| chr7:76056109 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1111T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056109 | |||||||
| chr7:76056110 | G | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1112G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056110 | |||||||
| chr7:76056111 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1113A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056111 | |||||||
| chr7:76056112 | G | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1114G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056112 | |||||||
| chr7:76056114 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1116A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056114 | |||||||
| chr7:76056115 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1117A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056115 | |||||||
| chr7:76056117 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1119T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056117 | |||||||
| chr7:76056118 | G | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1120G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056118 | |||||||
| chr7:76056120 | G | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1122G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056120 | |||||||
| chr7:76056124 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1126A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056124 | |||||||
| chr7:76056125 | G | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1127G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056125 | |||||||
| chr7:76056135 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1137T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056135 | |||||||
| chr7:76056140 | A | T | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1142A>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056140 | |||||||
| chr7:76056143 | A | T | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1145A>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056143 | |||||||
| chr7:76056148 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1150T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056148 | |||||||
| chr7:76056152 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1154A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056152 | |||||||
| chr7:76056157 | TGTAATTT others(82): Show |
T | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.235+1163_236-1161d others(91): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 76056157 | ||||||
| chr7:76056250 | C | T | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(114): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.236-1160C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056250 | |||||||
| chr7:76056275 | G | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(120): Show |
245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.236-1135G>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056275 | |||||||
| chr7:76056387 | C | G | 1 | a0002c0002t0002g0154 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.236-1023C>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056387 | |||||||
| chr7:76056398 | A | T | 24 | a0001c0001t0002g0190 a0002c0002t0002g0004 a0002c0002t0002g0006 others(21): Show |
46 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.236-1012A>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056398 | |||||||
| chr7:76056508 | C | T | 1 | a0002c0002t0002g0154 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.236-902C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056508 | |||||||
| chr7:76056535 | G | T | 1 | a0001c0001t0011g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.236-875G>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056535 | |||||||
| chr7:76056689 | G | A | 28 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(25): Show |
77 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.236-721G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056689 | |||||||
| chr7:76056779 | A | AACTC | 17 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0043 others(14): Show |
25 | HG00099.hp1 HG00140.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.236-630_236-629ins others(4): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 76056779 | ||||||
| chr7:76056781 | G | A | 17 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0043 others(14): Show |
25 | HG00099.hp1 HG00140.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.236-629G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76056781 | |||||||
| chr7:76057012 | CA | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(178): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.236-384delA | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 76057012 | ||||||
| chr7:76057143 | C | T | 1 | a0002c0002t0002g0066 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.236-267C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76057143 | |||||||
| chr7:76057292 | C | T | 2 | a0002c0002t0002g0050 a0002c0002t0002g0132 |
3 | HG02040.hp2 HG02135.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.236-118C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76057292 | |||||||
| chr7:76057316 | G | C | 1 | a0001c0001t0003g0081 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.236-94G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 2/8 | chr7 | 76057316 | |||||||
| chr7:76057576 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.319+83A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 3/8 | chr7 | 76057576 | |||||||
| chr7:76057658 | A | G | 6 | a0002c0002t0004g0024 a0002c0002t0004g0164 a0002c0002t0004g0166 others(3): Show |
9 | HG02258.hp2 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.319+165A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 3/8 | chr7 | 76057658 | |||||||
| chr7:76057667 | G | A | 1 | a0002c0002t0002g0063 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.319+174G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 3/8 | chr7 | 76057667 | |||||||
| chr7:76057704 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.319+211C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 3/8 | chr7 | 76057704 | |||||||
| chr7:76058225 | C | T | 1 | a0002c0002t0002g0031 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.429+147C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76058225 | |||||||
| chr7:76058396 | T | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG02129.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.429+318T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76058396 | |||||||
| chr7:76058397 | G | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0028 others(16): Show |
38 | HG00609.hp2 HG01934.hp2 HG01943.hp1 others(35): Show |
intron_variant | MODIFIER | c.429+319G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76058397 | |||||||
| chr7:76058407 | C | G | 17 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0043 others(14): Show |
25 | HG00099.hp1 HG00140.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.429+329C>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76058407 | |||||||
| chr7:76058483 | CCTGAACC others(20): Show |
C | 1 | a0001c0001t0001g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.429+430_429+456del others(27): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 76058483 | ||||||
| chr7:76058484 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0073 |
6 | HG01943.hp1 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+406C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76058484 | |||||||
| chr7:76058752 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.429+674G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76058752 | |||||||
| chr7:76058796 | GCAT | G | 15 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
23 | HG00099.hp1 HG00140.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.429+722_429+724del others(3): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 76058796 | ||||||
| chr7:76058812 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.429+734A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76058812 | |||||||
| chr7:76058906 | G | C | 1 | a0001c0001t0001g0176 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.429+828G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76058906 | |||||||
| chr7:76058909 | G | A | 4 | a0001c0001t0001g0051 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
5 | HG04199.hp1 HG04204.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.429+831G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76058909 | |||||||
| chr7:76059088 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.429+1010T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76059088 | |||||||
| chr7:76059096 | A | G | 4 | a0002c0002t0004g0024 a0002c0002t0004g0164 a0002c0002t0004g0166 others(1): Show |
6 | HG02258.hp2 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+1018A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76059096 | |||||||
| chr7:76059278 | C | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(120): Show |
245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.430-1095C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76059278 | |||||||
| chr7:76059305 | C | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(120): Show |
245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.430-1068C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76059305 | |||||||
| chr7:76059354 | G | A | 28 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(25): Show |
77 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.430-1019G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76059354 | |||||||
| chr7:76059442 | A | G | 1 | a0002c0002t0002g0137 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.430-931A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76059442 | |||||||
| chr7:76059636 | A | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(120): Show |
245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.430-737A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76059636 | |||||||
| chr7:76059705 | G | A | 2 | a0002c0002t0006g0068 a0002c0006t0006g0032 |
3 | HG02622.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.430-668G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76059705 | |||||||
| chr7:76060077 | C | T | 2 | a0001c0001t0005g0015 a0001c0001t0005g0107 |
5 | HG02559.hp2 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-296C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76060077 | |||||||
| chr7:76060118 | T | G | 1 | a0001c0001t0001g0108 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.430-255T>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76060118 | |||||||
| chr7:76060192 | C | T | 2 | a0001c0001t0001g0172 a0006c0011t0001g0182 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.430-181C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76060192 | |||||||
| chr7:76060291 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.430-82G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 4/8 | chr7 | 76060291 | |||||||
| chr7:76060746 | G | A | 5 | a0001c0001t0003g0017 a0001c0001t0003g0033 a0001c0001t0003g0070 others(2): Show |
9 | NA18948.hp1 NA18959.hp2 NA18977.hp2 others(6): Show |
intron_variant | MODIFIER | c.555+248G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76060746 | |||||||
| chr7:76060920 | G | C | 1 | a0001c0001t0001g0168 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.555+422G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76060920 | |||||||
| chr7:76060990 | C | T | 2 | a0001c0001t0003g0085 a0001c0001t0003g0093 |
2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.555+492C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76060990 | |||||||
| chr7:76061045 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.555+547G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76061045 | |||||||
| chr7:76061284 | T | C | 1 | a0001c0001t0007g0106 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.555+786T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76061284 | |||||||
| chr7:76061304 | G | A | 3 | a0002c0002t0002g0049 a0002c0002t0002g0146 a0002c0002t0002g0149 |
4 | NA18945.hp1 NA18986.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+806G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76061304 | |||||||
| chr7:76061342 | C | G | 1 | a0002c0002t0002g0148 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.555+844C>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76061342 | |||||||
| chr7:76061415 | CAG | C | 6 | a0002c0002t0004g0024 a0002c0002t0004g0164 a0002c0002t0004g0166 others(3): Show |
9 | HG02258.hp2 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.555+920_555+921del others(2): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 76061415 | ||||||
| chr7:76061513 | G | A | 1 | a0001c0001t0003g0074 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.555+1015G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76061513 | |||||||
| chr7:76061642 | T | TA | 17 | a0001c0001t0001g0026 a0001c0001t0001g0071 a0001c0001t0001g0095 others(14): Show |
24 | HG01175.hp2 HG01243.hp2 HG02559.hp2 others(21): Show |
intron_variant | MODIFIER | c.555+1160dupA | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 76061642 | ||||||
| chr7:76061668 | T | C | 1 | a0002c0002t0002g0130 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.555+1170T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76061668 | |||||||
| chr7:76061670 | A | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(29): Show |
83 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.555+1172A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76061670 | |||||||
| chr7:76061743 | A | ATCCCACC | 2 | a0002c0002t0006g0068 a0002c0006t0006g0032 |
3 | HG02622.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.555+1256_555+1262d others(9): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 76061743 | ||||||
| chr7:76061856 | A | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0171 a0001c0001t0001g0176 others(2): Show |
11 | HG00609.hp1 HG01496.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.555+1358A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76061856 | |||||||
| chr7:76061940 | T | C | 1 | a0002c0002t0002g0064 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.555+1442T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76061940 | |||||||
| chr7:76062103 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.556-1412G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76062103 | |||||||
| chr7:76062156 | C | T | 1 | a0002c0002t0002g0153 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.556-1359C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76062156 | |||||||
| chr7:76062196 | C | A | 6 | a0002c0002t0004g0024 a0002c0002t0004g0164 a0002c0002t0004g0166 others(3): Show |
9 | HG02258.hp2 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.556-1319C>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76062196 | |||||||
| chr7:76062402 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG01934.hp2 HG02040.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.556-1113G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76062402 | |||||||
| chr7:76062483 | C | T | 4 | a0002c0002t0004g0024 a0002c0002t0004g0164 a0002c0002t0004g0166 others(1): Show |
6 | HG02258.hp2 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-1032C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76062483 | |||||||
| chr7:76062524 | C | G | 1 | a0001c0001t0001g0040 | 2 | NA18952.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.556-991C>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76062524 | |||||||
| chr7:76062566 | A | C | 2 | a0001c0001t0003g0035 a0001c0001t0003g0075 |
3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.556-949A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76062566 | |||||||
| chr7:76062732 | T | C | 4 | a0002c0002t0004g0024 a0002c0002t0004g0164 a0002c0002t0004g0166 others(1): Show |
6 | HG02258.hp2 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-783T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76062732 | |||||||
| chr7:76062761 | A | G | 1 | a0002c0002t0002g0136 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.556-754A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76062761 | |||||||
| chr7:76062798 | G | A | 4 | a0001c0001t0001g0051 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
5 | HG04199.hp1 HG04204.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.556-717G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76062798 | |||||||
| chr7:76062941 | G | A | 7 | a0002c0002t0002g0022 a0002c0002t0002g0049 a0002c0002t0002g0126 others(4): Show |
10 | HG02074.hp2 NA18945.hp1 NA18966.hp1 others(7): Show |
intron_variant | MODIFIER | c.556-574G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76062941 | |||||||
| chr7:76062972 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.556-543C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76062972 | |||||||
| chr7:76063088 | T | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0172 a0001c0001t0001g0173 others(1): Show |
6 | HG02109.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.556-427T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76063088 | |||||||
| chr7:76063150 | A | G | 4 | a0002c0002t0004g0024 a0002c0002t0004g0164 a0002c0002t0004g0166 others(1): Show |
6 | HG02258.hp2 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-365A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76063150 | |||||||
| chr7:76063191 | C | T | 4 | a0001c0001t0005g0015 a0001c0001t0005g0107 a0001c0001t0007g0103 others(1): Show |
7 | HG02559.hp2 HG02970.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-324C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76063191 | |||||||
| chr7:76063192 | G | A | 4 | a0002c0002t0004g0024 a0002c0002t0004g0164 a0002c0002t0004g0166 others(1): Show |
6 | HG02258.hp2 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-323G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76063192 | |||||||
| chr7:76063347 | G | A | 1 | a0005c0009t0001g0180 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.556-168G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76063347 | |||||||
| chr7:76063494 | G | T | 6 | a0002c0002t0004g0024 a0002c0002t0004g0164 a0002c0002t0004g0166 others(3): Show |
9 | HG02258.hp2 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.556-21G>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 5/8 | chr7 | 76063494 | |||||||
| chr7:76063609 | C | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(121): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.633+17C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 6/8 | chr7 | 76063609 | |||||||
| chr7:76063647 | C | G | 6 | a0002c0002t0004g0024 a0002c0002t0004g0164 a0002c0002t0004g0166 others(3): Show |
9 | HG02258.hp2 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.633+55C>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 6/8 | chr7 | 76063647 | |||||||
| chr7:76063691 | C | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(121): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.633+99C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 6/8 | chr7 | 76063691 | |||||||
| chr7:76063719 | G | C | 1 | a0002c0002t0002g0066 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.633+127G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 6/8 | chr7 | 76063719 | |||||||
| chr7:76064064 | C | A | 1 | a0002c0006t0006g0032 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.634-275C>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 6/8 | chr7 | 76064064 | |||||||
| chr7:76064073 | T | G | 4 | a0001c0001t0001g0051 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
5 | HG04199.hp1 HG04204.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.634-266T>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 6/8 | chr7 | 76064073 | |||||||
| chr7:76064075 | G | A | 1 | a0002c0006t0006g0032 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.634-264G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 6/8 | chr7 | 76064075 | |||||||
| chr7:76064088 | C | T | 1 | a0001c0010t0003g0084 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.634-251C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 6/8 | chr7 | 76064088 | |||||||
| chr7:76064187 | A | G | 4 | a0001c0001t0001g0051 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
5 | HG04199.hp1 HG04204.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.634-152A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 6/8 | chr7 | 76064187 | |||||||
| chr7:76064306 | A | G | 2 | a0002c0002t0002g0061 a0002c0002t0002g0065 |
2 | HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.634-33A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 6/8 | chr7 | 76064306 | |||||||
| chr7:76064644 | C | T | 1 | a0002c0002t0002g0143 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.734-158C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 7/8 | chr7 | 76064644 | |||||||
| chr7:76064645 | T | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(121): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.734-157T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 7/8 | chr7 | 76064645 | |||||||
| chr7:76064761 | T | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(121): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.734-41T>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 7/8 | chr7 | 76064761 | |||||||
| chr7:76064967 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.885+14C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76064967 | |||||||
| chr7:76065027 | TC | T | 67 | a0001c0001t0002g0190 a0002c0002t0002g0001 a0002c0002t0002g0004 others(64): Show |
150 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.885+77delC | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 76065027 | ||||||
| chr7:76065054 | T | C | 2 | a0002c0002t0006g0068 a0002c0006t0006g0032 |
3 | HG02622.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.885+101T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065054 | |||||||
| chr7:76065260 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.885+307C>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065260 | |||||||
| chr7:76065280 | G | C | 1 | a0001c0008t0001g0189 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.885+327G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065280 | |||||||
| chr7:76065358 | CCTGAGTC others(26): Show |
C | 1 | a0002c0002t0002g0065 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.885+406_885+438del others(33): Show |
MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065358 | |||||||
| chr7:76065763 | G | A | 40 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(37): Show |
96 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.886-516G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065763 | |||||||
| chr7:76065784 | G | C | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-495G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065784 | |||||||
| chr7:76065788 | A | G | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-491A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065788 | |||||||
| chr7:76065790 | G | A | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-489G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065790 | |||||||
| chr7:76065791 | T | A | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-488T>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065791 | |||||||
| chr7:76065794 | G | T | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-485G>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065794 | |||||||
| chr7:76065801 | A | G | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-478A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065801 | |||||||
| chr7:76065802 | C | T | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-477C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065802 | |||||||
| chr7:76065804 | T | C | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-475T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065804 | |||||||
| chr7:76065805 | A | C | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-474A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065805 | |||||||
| chr7:76065807 | T | G | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-472T>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065807 | |||||||
| chr7:76065815 | A | T | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-464A>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065815 | |||||||
| chr7:76065816 | C | T | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-463C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065816 | |||||||
| chr7:76065817 | C | G | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-462C>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065817 | |||||||
| chr7:76065819 | G | A | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-460G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065819 | |||||||
| chr7:76065822 | T | A | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-457T>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065822 | |||||||
| chr7:76065826 | G | A | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-453G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065826 | |||||||
| chr7:76065830 | C | A | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-449C>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065830 | |||||||
| chr7:76065832 | G | C | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-447G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065832 | |||||||
| chr7:76065833 | T | A | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-446T>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065833 | |||||||
| chr7:76065834 | G | C | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-445G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065834 | |||||||
| chr7:76065835 | A | C | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-444A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065835 | |||||||
| chr7:76065843 | T | A | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-436T>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065843 | |||||||
| chr7:76065850 | C | T | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-429C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065850 | |||||||
| chr7:76065854 | A | G | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-425A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065854 | |||||||
| chr7:76065856 | C | T | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-423C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065856 | |||||||
| chr7:76065864 | G | A | 1 | a0001c0001t0003g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.886-415G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065864 | |||||||
| chr7:76065865 | G | A | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-414G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065865 | |||||||
| chr7:76065867 | G | C | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-412G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065867 | |||||||
| chr7:76065871 | G | T | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-408G>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065871 | |||||||
| chr7:76065873 | C | T | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-406C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065873 | |||||||
| chr7:76065875 | A | T | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-404A>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065875 | |||||||
| chr7:76065878 | A | T | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-401A>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065878 | |||||||
| chr7:76065882 | A | T | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-397A>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065882 | |||||||
| chr7:76065884 | A | C | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-395A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065884 | |||||||
| chr7:76065885 | A | C | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-394A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065885 | |||||||
| chr7:76065886 | A | T | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-393A>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065886 | |||||||
| chr7:76065888 | A | C | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-391A>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065888 | |||||||
| chr7:76065889 | G | T | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-390G>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065889 | |||||||
| chr7:76065892 | T | C | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-387T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065892 | |||||||
| chr7:76065893 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0112 |
2 | HG03831.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.886-386C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065893 | |||||||
| chr7:76065894 | T | A | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-385T>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065894 | |||||||
| chr7:76065895 | G | C | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-384G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065895 | |||||||
| chr7:76065896 | T | C | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-383T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065896 | |||||||
| chr7:76065898 | G | C | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-381G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065898 | |||||||
| chr7:76065899 | G | A | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-380G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065899 | |||||||
| chr7:76065901 | G | C | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-378G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065901 | |||||||
| chr7:76065903 | G | A | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-376G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065903 | |||||||
| chr7:76065904 | A | T | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-375A>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065904 | |||||||
| chr7:76065905 | A | T | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-374A>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065905 | |||||||
| chr7:76065907 | A | G | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-372A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065907 | |||||||
| chr7:76065909 | G | T | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-370G>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065909 | |||||||
| chr7:76065914 | A | G | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-365A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065914 | |||||||
| chr7:76065916 | T | C | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-363T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065916 | |||||||
| chr7:76065917 | G | A | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-362G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065917 | |||||||
| chr7:76065918 | T | G | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-361T>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065918 | |||||||
| chr7:76065924 | A | T | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-355A>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065924 | |||||||
| chr7:76065930 | G | T | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-349G>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065930 | |||||||
| chr7:76065931 | A | G | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-348A>G | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065931 | |||||||
| chr7:76065932 | G | C | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-347G>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065932 | |||||||
| chr7:76065934 | T | C | 1 | a0002c0002t0002g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.886-345T>C | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065934 | |||||||
| chr7:76065966 | C | T | 1 | a0001c0010t0003g0084 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.886-313C>T | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76065966 | |||||||
| chr7:76066209 | G | A | 1 | a0002c0006t0006g0032 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.886-70G>A | MDH2 | ENSG00000146701.12 | transcript | ENST00000315758.10 | protein_coding | 8/8 | chr7 | 76066209 |