Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10797 |
| ensemblid | ENSG00000065911.13 |
| hgncid | 7434 |
| symbol | MTHFD2 |
| name | methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase |
| refseq_nuc | NM_006636.4 |
| refseq_prot | NP_006627.2 |
| ensembl_nuc | ENST00000394053.7 |
| ensembl_prot | ENSP00000377617.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 74198615 |
| end | 74217565 |
| strand | + |
| ver | v1.2 |
| region | chr2:74198615-74217565 |
| region5000 | chr2:74193615-74222565 |
| regionname0 | MTHFD2_chr2_74198615_74217565 |
| regionname5000 | MTHFD2_chr2_74193615_74222565 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 350 | 412 | 93 | 74 | 196 | 10 | 37 | 150 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | MAATS others(345): Show |
chr2 | 74193615 | 74222565 |
| a0002 | 0/0 | 350 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | MAATS others(345): Show |
chr2 | 74193615 | 74222565 |
| a0003 | 0/0 | 350 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | MAATS others(345): Show |
chr2 | 74193615 | 74222565 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1050 | 412 | 93 | 74 | 196 | 10 | 37 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | ATGGC others(1045): Show |
chr2 | 74193615 | 74222565 | ||
| a0002c0003 | 0/0 | 1050 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | ATGGC others(1045): Show |
chr2 | 74193615 | 74222565 | ||
| a0003c0002 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | ATGGC others(1045): Show |
chr2 | 74193615 | 74222565 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4403 | 212 | 15 | 40 | 123 | 6 | 26 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0002 | 0/0 | 4403 | 72 | 13 | 12 | 38 | 4 | 5 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0003 | 0/0 | 4403 | 52 | 8 | 18 | 24 | 0 | 2 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0004 | 0/0 | 4404 | 14 | 14 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4399): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0005 | 0/0 | 4404 | 9 | 6 | 0 | 3 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4399): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0006 | 0/0 | 4403 | 8 | 8 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0007 | 0/0 | 4403 | 7 | 6 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0008 | 0/0 | 4404 | 6 | 6 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4399): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0009 | 0/0 | 4403 | 3 | 0 | 0 | 3 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0010 | 0/0 | 4403 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0011 | 0/0 | 4403 | 3 | 2 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0012 | 0/0 | 4404 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4399): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0013 | 0/0 | 4403 | 2 | 1 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0014 | 0/0 | 4403 | 2 | 1 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0015 | 0/0 | 4403 | 2 | 0 | 0 | 0 | 0 | 2 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0016 | 0/0 | 4403 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0017 | 0/0 | 4404 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4399): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0018 | 0/0 | 4403 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0019 | 0/0 | 4403 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0020 | 0/0 | 4403 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0021 | 0/0 | 4403 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0022 | 0/0 | 4403 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0023 | 0/0 | 4403 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0024 | 0/0 | 4403 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0025 | 0/0 | 4403 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0026 | 0/0 | 4403 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0027 | 0/0 | 4403 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0028 | 0/0 | 4403 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0001c0001t0029 | 0/0 | 4404 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4399): Show |
chr2 | 74193615 | 74222565 |
| a0002c0003t0001 | 0/0 | 4403 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4398): Show |
chr2 | 74193615 | 74222565 |
| a0003c0002t0004 | 0/0 | 4404 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | CTCCC others(4399): Show |
chr2 | 74193615 | 74222565 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 24 | 0 | 5 | 15 | 0 | 3 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0003 | 1/0 | 17 | 1 | 6 | 5 | 1 | 3 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0007 | 0/0 | 7 | 1 | 2 | 4 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0008 | 0/0 | 6 | 3 | 0 | 3 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0022 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0002 | 0/0 | 21 | 1 | 1 | 19 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0004 | 0/0 | 13 | 3 | 6 | 0 | 2 | 2 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0006 | 0/0 | 7 | 1 | 3 | 0 | 2 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0009 | 0/0 | 6 | 2 | 4 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0004g0005 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0005g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0006g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0007g0050 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0008g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0008g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0008g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0008g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0009g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0009g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0009g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0010g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0010g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0010g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0011g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0011g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0012g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0013g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0013g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0014g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0014g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0015g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0015g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0016g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0017g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0018g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0019g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0020g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0021g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0022g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0023g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0024g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0025g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0026g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0027g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0028g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0001c0001t0029g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0002c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| a0003c0002t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | FIN | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0127 | EAS | CHS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | CHS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | CHS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | CHS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00609 | hp2 | a0001 | c0001 | t0009 | g0041 | EAS | CHS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00735 | hp1 | a0001 | c0001 | t0014 | g0227 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01099 | hp2 | a0001 | c0001 | t0011 | g0098 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0050 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0116 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01243 | hp1 | a0001 | c0001 | t0013 | g0228 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01884 | hp1 | a0001 | c0001 | t0023 | g0231 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0036 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0117 | AMR | PEL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0049 | AMR | PEL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0049 | AMR | PEL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02071 | hp1 | a0001 | c0001 | t0009 | g0003 | EAS | KHV | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | KHV | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | KHV | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | KHV | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0222 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0104 | AMR | PEL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02155 | hp1 | a0001 | c0001 | t0019 | g0038 | EAS | CDX | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CDX | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | CDX | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02257 | hp1 | a0001 | c0001 | t0010 | g0223 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02257 | hp2 | a0001 | c0001 | t0017 | g0005 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02258 | hp1 | a0001 | c0001 | t0013 | g0230 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0050 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02451 | hp1 | a0001 | c0001 | t0012 | g0025 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0201 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | KHV | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0197 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0110 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0112 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0229 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0200 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02818 | hp1 | a0001 | c0001 | t0008 | g0219 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0181 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02886 | hp2 | a0001 | c0001 | t0016 | g0052 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0054 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0054 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0206 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02922 | hp2 | a0001 | c0001 | t0011 | g0006 | AFR | ESN | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | ESN | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0208 | AFR | ESN | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0179 | AFR | ESN | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | ESN | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03041 | hp2 | a0001 | c0001 | t0027 | g0236 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0053 | AFR | MSL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03098 | hp2 | a0001 | c0001 | t0020 | g0085 | AFR | MSL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0232 | AFR | ESN | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03139 | hp1 | a0001 | c0001 | t0016 | g0052 | AFR | ESN | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ESN | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | ESN | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03209 | hp2 | a0001 | c0001 | t0010 | g0225 | AFR | MSL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03225 | hp1 | a0001 | c0001 | t0010 | g0224 | AFR | MSL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03225 | hp2 | a0001 | c0001 | t0029 | g0218 | AFR | MSL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03453 | hp1 | a0001 | c0001 | t0014 | g0100 | AFR | MSL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0180 | AFR | MSL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0202 | AFR | MSL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0053 | AFR | MSL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03490 | hp1 | a0001 | c0001 | t0015 | g0011 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0198 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03491 | hp1 | a0001 | c0001 | t0015 | g0095 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | MSL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | MSL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | STU | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03831 | hp1 | a0002 | c0003 | t0001 | g0178 | SAS | BEB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03927 | hp2 | a0001 | c0001 | t0025 | g0137 | SAS | BEB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | STU | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | STU | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG04228 | hp1 | a0001 | c0001 | t0022 | g0003 | SAS | STU | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | STU | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0036 | AFR | YRI | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18522 | hp2 | a0001 | c0001 | t0012 | g0025 | AFR | YRI | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | CHB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | CHB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | YRI | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | YRI | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18948 | hp1 | a0001 | c0001 | t0005 | g0133 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18951 | hp1 | a0001 | c0001 | t0009 | g0169 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18976 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18976 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18977 | hp2 | a0001 | c0001 | t0018 | g0067 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18978 | hp1 | a0001 | c0001 | t0028 | g0094 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19004 | hp2 | a0001 | c0001 | t0024 | g0184 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19007 | hp2 | a0001 | c0001 | t0021 | g0056 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0233 | AFR | LWK | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0235 | AFR | LWK | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | LWK | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0114 | AFR | YRI | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0113 | AFR | YRI | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ASW | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0234 | AFR | ASW | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | TSI | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | TSI | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | TSI | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0221 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0207 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | MSL | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | USA | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| HG06807 | hp2 | a0001 | c0001 | t0011 | g0006 | AFR | USA | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | USA | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA20300 | hp2 | a0003 | c0002 | t0004 | g0005 | AFR | USA | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA21309 | hp1 | a0001 | c0001 | t0026 | g0220 | AFR | LWK | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0003 | REF | REF | MTHFD2_chr2_74193615_74222565 | MTHFD2 | chr2 | 74193615 | 74222565 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:74208650 | G | A | 1 | a0003 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.491G>A | p.Arg164Gln | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 4/8 | 518/4403 | 491/1053 | 164/350 | chr2 | 74208650 | |||
| chr2:74214186 | A | G | 1 | a0002 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.997A>G | p.Arg333Gly | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 1024/4403 | 997/1053 | 333/350 | chr2 | 74214186 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:74198638 | G | A | 1 | a0001c0001t0017 | 1 | HG02257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-4G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/8 | 4 | chr2 | 74198638 | ||||||
| chr2:74214477 | T | G | 1 | a0001c0001t0012 | 2 | HG02451.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*235T>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 235 | chr2 | 74214477 | ||||||
| chr2:74214583 | A | G | 1 | a0001c0001t0029 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*341A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 341 | chr2 | 74214583 | ||||||
| chr2:74214599 | A | G | 1 | a0001c0001t0028 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*357A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 357 | chr2 | 74214599 | ||||||
| chr2:74214672 | A | G | 9 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(6): Show |
97 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*430A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 430 | chr2 | 74214672 | ||||||
| chr2:74214776 | C | T | 3 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0027 |
11 | HG00735.hp1 HG02615.hp2 HG02965.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*534C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 534 | chr2 | 74214776 | ||||||
| chr2:74214951 | T | C | 1 | a0001c0001t0008 | 6 | HG02717.hp2 HG02818.hp1 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*709T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 709 | chr2 | 74214951 | ||||||
| chr2:74215226 | G | C | 1 | a0001c0001t0015 | 2 | HG03490.hp1 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*984G>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 984 | chr2 | 74215226 | ||||||
| chr2:74215280 | A | G | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(19): Show |
184 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*1038A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 1038 | chr2 | 74215280 | ||||||
| chr2:74215304 | T | G | 18 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(15): Show |
168 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*1062T>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 1062 | chr2 | 74215304 | ||||||
| chr2:74215423 | A | AT | 7 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0008 others(4): Show |
34 | HG00408.hp1 HG01891.hp1 HG02055.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1198dupT | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 1199 | INFO_REALIGN_3_PRIME | chr2 | 74215423 | |||||
| chr2:74215544 | C | T | 1 | a0001c0001t0012 | 2 | HG02451.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1302C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 1302 | chr2 | 74215544 | ||||||
| chr2:74215610 | C | G | 1 | a0001c0001t0022 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1368C>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 1368 | chr2 | 74215610 | ||||||
| chr2:74215625 | T | A | 1 | a0001c0001t0023 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1383T>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 1383 | chr2 | 74215625 | ||||||
| chr2:74215671 | T | C | 1 | a0001c0001t0026 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1429T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 1429 | chr2 | 74215671 | ||||||
| chr2:74215738 | A | G | 1 | a0001c0001t0021 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1496A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 1496 | chr2 | 74215738 | ||||||
| chr2:74215753 | T | A | 1 | a0001c0001t0011 | 3 | HG01099.hp2 HG02922.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1511T>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 1511 | chr2 | 74215753 | ||||||
| chr2:74215783 | G | A | 2 | a0001c0001t0003 a0001c0001t0024 |
53 | HG00558.hp2 HG00597.hp2 HG00741.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1541G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 1541 | chr2 | 74215783 | ||||||
| chr2:74215884 | C | T | 1 | a0001c0001t0020 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1642C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 1642 | chr2 | 74215884 | ||||||
| chr2:74215924 | T | C | 3 | a0001c0001t0003 a0001c0001t0024 a0001c0001t0025 |
54 | HG00558.hp2 HG00597.hp2 HG00741.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1682T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 1682 | chr2 | 74215924 | ||||||
| chr2:74215997 | T | G | 1 | a0001c0001t0024 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1755T>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 1755 | chr2 | 74215997 | ||||||
| chr2:74216151 | G | C | 1 | a0001c0001t0027 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1909G>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 1909 | chr2 | 74216151 | ||||||
| chr2:74216307 | A | G | 4 | a0001c0001t0004 a0001c0001t0017 a0001c0001t0029 others(1): Show |
17 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2065A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 2065 | chr2 | 74216307 | ||||||
| chr2:74216341 | T | C | 1 | a0001c0001t0018 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2099T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 2099 | chr2 | 74216341 | ||||||
| chr2:74216342 | G | A | 1 | a0001c0001t0014 | 2 | HG00735.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2100G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 2100 | chr2 | 74216342 | ||||||
| chr2:74216415 | C | T | 1 | a0001c0001t0015 | 2 | HG03490.hp1 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2173C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 2173 | chr2 | 74216415 | ||||||
| chr2:74216483 | A | G | 4 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0023 others(1): Show |
7 | HG00735.hp1 HG01884.hp1 HG02257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2241A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 2241 | chr2 | 74216483 | ||||||
| chr2:74216508 | G | A | 1 | a0001c0001t0009 | 3 | HG00609.hp2 HG02071.hp1 NA18951.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2266G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 2266 | chr2 | 74216508 | ||||||
| chr2:74216603 | T | A | 1 | a0001c0001t0019 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2361T>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 2361 | chr2 | 74216603 | ||||||
| chr2:74216634 | G | A | 1 | a0001c0001t0012 | 2 | HG02451.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2392G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 2392 | chr2 | 74216634 | ||||||
| chr2:74216856 | C | T | 1 | a0001c0001t0007 | 7 | HG01109.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2614C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 2614 | chr2 | 74216856 | ||||||
| chr2:74217102 | C | T | 1 | a0001c0001t0008 | 6 | HG02717.hp2 HG02818.hp1 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2860C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 2860 | chr2 | 74217102 | ||||||
| chr2:74217174 | T | G | 4 | a0001c0001t0004 a0001c0001t0017 a0001c0001t0029 others(1): Show |
17 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2932T>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 2932 | chr2 | 74217174 | ||||||
| chr2:74217304 | A | T | 4 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0015 others(1): Show |
78 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*3062A>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 8/8 | 3062 | chr2 | 74217304 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:74198805 | G | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(41): Show |
88 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.101+63G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74198805 | |||||||
| chr2:74198820 | G | T | 5 | a0001c0001t0001g0055 a0001c0001t0001g0237 a0001c0001t0001g0238 others(2): Show |
6 | HG01099.hp1 HG01168.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.101+78G>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74198820 | |||||||
| chr2:74198882 | G | A | 1 | a0001c0001t0021g0056 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.101+140G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74198882 | |||||||
| chr2:74198911 | G | A | 28 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0006 others(25): Show |
77 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.101+169G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74198911 | |||||||
| chr2:74198973 | A | C | 1 | a0001c0001t0027g0236 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.101+231A>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74198973 | |||||||
| chr2:74198995 | C | G | 1 | a0001c0001t0002g0103 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.101+253C>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74198995 | |||||||
| chr2:74199170 | T | C | 1 | a0001c0001t0027g0236 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.101+428T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74199170 | |||||||
| chr2:74199352 | A | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(41): Show |
87 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.101+610A>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74199352 | |||||||
| chr2:74199707 | C | CA | 12 | a0001c0001t0001g0033 a0001c0001t0001g0105 a0001c0001t0001g0106 others(9): Show |
13 | HG00544.hp1 HG00735.hp2 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+987dupA | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74199707 | ||||||
| chr2:74199707 | CA | C | 9 | a0001c0001t0001g0051 a0001c0001t0001g0210 a0001c0001t0001g0211 others(6): Show |
10 | HG02523.hp1 HG03017.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.101+987delA | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74199707 | ||||||
| chr2:74199707 | CAA | C | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(6): Show |
10 | HG01175.hp1 HG01433.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.101+986_101+987del others(2): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74199707 | ||||||
| chr2:74199707 | CAAA | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(75): Show |
178 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.101+985_101+987del others(3): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74199707 | ||||||
| chr2:74199707 | CAAAA | C | 8 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0006g0015 others(5): Show |
11 | HG01884.hp1 HG02615.hp2 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.101+984_101+987del others(4): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74199707 | ||||||
| chr2:74199871 | A | G | 1 | a0001c0001t0003g0209 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.101+1129A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74199871 | |||||||
| chr2:74199918 | T | C | 12 | a0001c0001t0004g0005 a0001c0001t0004g0221 a0001c0001t0004g0222 others(9): Show |
20 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.101+1176T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74199918 | |||||||
| chr2:74199932 | C | T | 1 | a0001c0001t0027g0236 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.101+1190C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74199932 | |||||||
| chr2:74199997 | A | G | 1 | a0001c0001t0027g0236 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.101+1255A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74199997 | |||||||
| chr2:74200127 | G | A | 7 | a0001c0001t0004g0005 a0001c0001t0004g0221 a0001c0001t0004g0222 others(4): Show |
15 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.101+1385G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74200127 | |||||||
| chr2:74200200 | C | T | 1 | a0001c0001t0027g0236 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.101+1458C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74200200 | |||||||
| chr2:74200216 | T | A | 5 | a0001c0001t0003g0034 a0001c0001t0003g0104 a0001c0001t0003g0115 others(2): Show |
6 | HG01070.hp1 HG01175.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+1474T>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74200216 | |||||||
| chr2:74200343 | TCTTTTCA | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0086 |
4 | NA18970.hp1 NA18981.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.101+1604_101+1610d others(9): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74200343 | ||||||
| chr2:74200396 | GCAATCCA others(16): Show |
G | 1 | a0001c0001t0001g0086 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.101+1657_101+1679d others(25): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74200396 | ||||||
| chr2:74200441 | A | G | 1 | a0001c0001t0012g0025 | 2 | HG02451.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.101+1699A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74200441 | |||||||
| chr2:74200491 | A | AAATACTG others(318): Show |
1 | a0001c0001t0002g0101 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.101+1765_101+1766i others(327): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74200491 | ||||||
| chr2:74200491 | A | AAATACTG others(335): Show |
1 | a0001c0001t0002g0102 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.101+1765_101+1766i others(344): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74200491 | ||||||
| chr2:74200589 | C | T | 1 | a0001c0001t0020g0085 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.101+1847C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74200589 | |||||||
| chr2:74200719 | G | A | 1 | a0001c0001t0004g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.101+1977G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74200719 | |||||||
| chr2:74200888 | T | C | 47 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0006 others(44): Show |
107 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.101+2146T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74200888 | |||||||
| chr2:74200926 | G | GTAC | 3 | a0001c0001t0006g0232 a0001c0001t0006g0233 a0001c0001t0006g0234 |
3 | HG03130.hp2 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.101+2186_101+2188d others(5): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74200926 | ||||||
| chr2:74200967 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.101+2225C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74200967 | |||||||
| chr2:74201132 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.101+2390C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74201132 | |||||||
| chr2:74201203 | G | T | 12 | a0001c0001t0007g0050 a0001c0001t0007g0113 a0001c0001t0007g0114 others(9): Show |
15 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.101+2461G>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74201203 | |||||||
| chr2:74201523 | A | AT | 37 | a0001c0001t0001g0082 a0001c0001t0002g0002 a0001c0001t0002g0004 others(34): Show |
87 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.101+2795dupT | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74201523 | ||||||
| chr2:74201523 | AT | A | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0105 others(4): Show |
7 | HG01070.hp2 HG02015.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+2795delT | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74201523 | ||||||
| chr2:74201567 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.101+2825G>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74201567 | |||||||
| chr2:74201573 | C | T | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | NA18951.hp2 NA18954.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.101+2831C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74201573 | |||||||
| chr2:74201779 | T | C | 4 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0219 others(1): Show |
6 | HG02717.hp2 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+3037T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74201779 | |||||||
| chr2:74201781 | C | G | 1 | a0001c0001t0026g0220 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.101+3039C>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74201781 | |||||||
| chr2:74201912 | C | T | 1 | a0001c0001t0027g0236 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.101+3170C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74201912 | |||||||
| chr2:74201958 | C | CT | 37 | a0001c0001t0003g0009 a0001c0001t0003g0014 a0001c0001t0003g0044 others(34): Show |
51 | HG00558.hp2 HG00597.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.101+3229dupT | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74201958 | ||||||
| chr2:74201958 | CT | C | 7 | a0001c0001t0001g0066 a0001c0001t0001g0120 a0001c0001t0001g0121 others(4): Show |
7 | HG01257.hp1 HG02735.hp2 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+3229delT | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74201958 | ||||||
| chr2:74202051 | T | C | 1 | a0001c0001t0006g0235 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.101+3309T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74202051 | |||||||
| chr2:74202065 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(134): Show |
256 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(253): Show |
intron_variant | MODIFIER | c.101+3323C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74202065 | |||||||
| chr2:74202269 | T | C | 1 | a0001c0001t0012g0025 | 2 | HG02451.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.102-3436T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74202269 | |||||||
| chr2:74202342 | T | C | 1 | a0001c0001t0002g0090 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.102-3363T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74202342 | |||||||
| chr2:74202353 | A | G | 4 | a0001c0001t0005g0110 a0001c0001t0005g0179 a0001c0001t0005g0180 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.102-3352A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74202353 | |||||||
| chr2:74202413 | G | C | 33 | a0001c0001t0003g0009 a0001c0001t0003g0014 a0001c0001t0003g0044 others(30): Show |
47 | HG00558.hp2 HG00597.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.102-3292G>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74202413 | |||||||
| chr2:74202419 | T | C | 1 | a0001c0001t0018g0067 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.102-3286T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74202419 | |||||||
| chr2:74202743 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.102-2962G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74202743 | |||||||
| chr2:74202813 | A | T | 1 | a0001c0001t0003g0199 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.102-2892A>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74202813 | |||||||
| chr2:74202933 | A | T | 4 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0219 others(1): Show |
6 | HG02717.hp2 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-2772A>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74202933 | |||||||
| chr2:74203013 | T | C | 1 | a0001c0001t0003g0183 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.102-2692T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74203013 | |||||||
| chr2:74203099 | C | T | 1 | a0001c0001t0002g0032 | 2 | NA18948.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.102-2606C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74203099 | |||||||
| chr2:74203259 | G | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(38): Show |
83 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.102-2446G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74203259 | |||||||
| chr2:74203451 | G | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0081 a0001c0001t0018g0067 |
6 | NA18949.hp1 NA18960.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-2254G>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74203451 | |||||||
| chr2:74203843 | C | CTAGTT | 7 | a0001c0001t0001g0023 a0001c0001t0001g0145 a0001c0001t0001g0146 others(4): Show |
9 | HG00621.hp2 HG00741.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.102-1801_102-1797d others(7): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTAGTTTA others(3): Show |
2 | a0001c0001t0001g0040 a0001c0001t0001g0124 |
3 | HG02738.hp2 NA18946.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.102-1806_102-1797d others(12): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTAGTTTA others(8): Show |
3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0005g0110 |
3 | HG01346.hp2 HG01358.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.102-1811_102-1797d others(17): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTAGTTTA others(13): Show |
1 | a0001c0001t0001g0153 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.102-1816_102-1797d others(22): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTAGTTTA others(23): Show |
1 | a0001c0001t0001g0154 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.102-1826_102-1797d others(32): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTAGTTTA others(28): Show |
1 | a0001c0001t0001g0213 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.102-1831_102-1797d others(37): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTAGTTTA others(33): Show |
1 | a0001c0001t0001g0155 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.102-1836_102-1797d others(42): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTAGTTTA others(38): Show |
3 | a0001c0001t0001g0041 a0001c0001t0001g0156 a0001c0001t0009g0041 |
3 | HG00609.hp2 NA18965.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.102-1841_102-1797d others(47): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTAGTTTA others(43): Show |
4 | a0001c0001t0001g0122 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | HG01256.hp1 HG03239.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.102-1846_102-1797d others(52): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTAGTTTA others(48): Show |
3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0003g0034 |
4 | HG01257.hp2 HG01258.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-1851_102-1797d others(57): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTAGTTTA others(53): Show |
1 | a0001c0001t0001g0024 | 2 | NA18976.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.102-1856_102-1797d others(62): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTAGTTTA others(58): Show |
4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG00733.hp1 HG02132.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-1861_102-1797d others(67): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTAGTTTA others(63): Show |
5 | a0001c0001t0001g0033 a0001c0001t0001g0109 a0001c0001t0001g0164 others(2): Show |
6 | HG00408.hp2 HG00735.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-1797_102-1796i others(72): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTAGTTTA others(68): Show |
2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | NA18957.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.102-1797_102-1796i others(77): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTAGTTTA others(73): Show |
1 | a0001c0001t0001g0167 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.102-1797_102-1796i others(82): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTAGTTTA others(78): Show |
4 | a0001c0001t0001g0042 a0001c0001t0001g0168 a0001c0001t0001g0170 others(1): Show |
5 | HG02148.hp1 NA18951.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.102-1797_102-1796i others(87): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTAGTTTA others(83): Show |
5 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0171 others(2): Show |
7 | HG00438.hp2 HG04115.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.102-1797_102-1796i others(92): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTAGTTTA others(88): Show |
5 | a0001c0001t0001g0105 a0001c0001t0001g0123 a0001c0001t0001g0173 others(2): Show |
5 | HG02040.hp2 HG02300.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.102-1797_102-1796i others(97): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTAGTTTA others(93): Show |
1 | a0001c0001t0001g0215 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.102-1797_102-1796i others(102): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTAGTTTA others(98): Show |
2 | a0001c0001t0001g0106 a0001c0001t0001g0176 |
2 | NA18949.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.102-1797_102-1796i others(107): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTAGTTTA others(103): Show |
1 | a0001c0001t0001g0177 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.102-1797_102-1796i others(112): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTATTTTA others(3): Show |
11 | a0001c0001t0001g0068 a0001c0001t0003g0057 a0001c0001t0004g0221 others(8): Show |
13 | HG00642.hp2 HG00735.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.102-1860_102-1859i others(12): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTATTTTA others(8): Show |
76 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(73): Show |
133 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.102-1860_102-1859i others(17): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTATTTTA others(13): Show |
5 | a0001c0001t0003g0009 a0001c0001t0003g0045 a0001c0001t0003g0182 others(2): Show |
11 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.102-1860_102-1859i others(22): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | C | CTATTTTA others(13): Show |
15 | a0001c0001t0003g0014 a0001c0001t0003g0048 a0001c0001t0003g0049 others(12): Show |
20 | HG01081.hp2 HG01952.hp2 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.102-1860_102-1859i others(22): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | CTAGTT | C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0037 others(5): Show |
14 | HG00280.hp1 HG00738.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.102-1801_102-1797d others(7): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | CTAGTTTA others(3): Show |
C | 8 | a0001c0001t0001g0020 a0001c0001t0001g0107 a0001c0001t0001g0120 others(5): Show |
11 | HG00544.hp1 HG01081.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.102-1806_102-1797d others(12): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203843 | CTAGTTTA others(8): Show |
C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0126 a0001c0001t0005g0127 |
4 | HG00408.hp1 HG02647.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-1811_102-1797d others(17): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203843 | ||||||
| chr2:74203846 | G | T | 31 | a0001c0001t0001g0086 a0001c0001t0002g0002 a0001c0001t0002g0004 others(28): Show |
81 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.102-1859G>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74203846 | |||||||
| chr2:74203851 | G | T | 30 | a0001c0001t0001g0086 a0001c0001t0002g0002 a0001c0001t0002g0004 others(27): Show |
79 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.102-1854G>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74203851 | |||||||
| chr2:74203854 | T | TAGTTGAG others(3): Show |
1 | a0001c0001t0001g0125 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.102-1847_102-1846i others(12): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203854 | ||||||
| chr2:74203854 | T | TAGTTTAG others(63): Show |
1 | a0001c0001t0001g0144 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.102-1797_102-1796i others(72): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203854 | ||||||
| chr2:74203856 | G | GTTTAGTT others(10): Show |
1 | a0002c0003t0001g0178 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.102-1847_102-1831d others(19): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203856 | ||||||
| chr2:74203856 | G | T | 2 | a0001c0001t0001g0086 a0001c0001t0002g0089 |
2 | HG02976.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.102-1849G>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74203856 | |||||||
| chr2:74203857 | TTTAGTTT others(42): Show |
T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(34): Show |
76 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.102-1825_102-1777d others(51): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203857 | ||||||
| chr2:74203862 | TTTAGTTT others(37): Show |
T | 22 | a0001c0001t0001g0010 a0001c0001t0001g0058 a0001c0001t0001g0059 others(19): Show |
31 | HG01069.hp1 HG01109.hp1 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.102-1820_102-1777d others(46): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203862 | ||||||
| chr2:74203867 | TTTAGTTT others(32): Show |
T | 10 | a0001c0001t0001g0068 a0001c0001t0003g0047 a0001c0001t0003g0193 others(7): Show |
12 | HG00642.hp2 HG00735.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.102-1815_102-1777d others(41): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203867 | ||||||
| chr2:74203872 | TTTAGTTT others(27): Show |
T | 4 | a0001c0001t0001g0086 a0001c0001t0003g0194 a0001c0001t0003g0195 others(1): Show |
4 | HG02451.hp1 NA18941.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.102-1810_102-1777d others(36): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203872 | ||||||
| chr2:74203877 | TTTAGTTT others(22): Show |
T | 22 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(19): Show |
29 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.102-1805_102-1777d others(31): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203877 | ||||||
| chr2:74203882 | TTTAGTTT others(17): Show |
T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0006 others(38): Show |
85 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.102-1800_102-1777d others(26): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203882 | ||||||
| chr2:74203886 | GTTTAGTT others(4): Show |
G | 1 | a0001c0001t0001g0008 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.102-1816_102-1806d others(13): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203886 | ||||||
| chr2:74203887 | TTTAGTTT others(12): Show |
T | 6 | a0001c0001t0002g0006 a0001c0001t0003g0009 a0001c0001t0003g0045 others(3): Show |
11 | HG00558.hp2 HG00741.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.102-1796_102-1778d others(21): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203887 | ||||||
| chr2:74203891 | GTTTAGTT others(13): Show |
G | 2 | a0001c0001t0001g0003 a0001c0001t0025g0137 |
2 | HG01433.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.102-1811_102-1792d others(22): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203891 | ||||||
| chr2:74203892 | TTTAGTTT others(7): Show |
T | 5 | a0001c0001t0002g0088 a0001c0001t0003g0014 a0001c0001t0003g0049 others(2): Show |
6 | HG01243.hp1 HG01243.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-1796_102-1783d others(16): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203892 | ||||||
| chr2:74203896 | GT | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0139 |
4 | HG02486.hp2 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-1806delT | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203896 | ||||||
| chr2:74203896 | GTTTAGTT others(8): Show |
G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0118 |
4 | HG01070.hp2 HG03688.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.102-1806_102-1792d others(17): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203896 | ||||||
| chr2:74203901 | GTTTAGTT others(3): Show |
G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0138 |
4 | HG01069.hp2 HG02135.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.102-1801_102-1792d others(12): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203901 | ||||||
| chr2:74203902 | TTTAG | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0139 others(1): Show |
7 | HG02004.hp2 HG02273.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.102-1796_102-1793d others(6): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203902 | ||||||
| chr2:74203904 | T | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0039 |
4 | HG04228.hp2 NA18953.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.102-1801T>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74203904 | |||||||
| chr2:74203905 | A | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0039 |
4 | HG04228.hp2 NA18953.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.102-1800A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74203905 | |||||||
| chr2:74203906 | G | GT | 10 | a0001c0001t0001g0038 a0001c0001t0001g0132 a0001c0001t0001g0134 others(7): Show |
10 | HG02155.hp1 HG03831.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.102-1797dupT | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203906 | ||||||
| chr2:74203906 | G | GTTAGT | 3 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0039 |
3 | HG01517.hp1 HG04204.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.102-1781_102-1777d others(7): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203906 | ||||||
| chr2:74203906 | G | GTTTAGTT others(4): Show |
1 | a0001c0001t0001g0008 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.102-1797_102-1796i others(13): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203906 | ||||||
| chr2:74203906 | G | GTTTAGTT others(8): Show |
3 | a0001c0001t0001g0140 a0001c0001t0003g0115 a0001c0001t0003g0116 |
3 | HG01070.hp1 HG01175.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.102-1797_102-1796i others(17): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203906 | ||||||
| chr2:74203906 | G | GTTTAGTT others(23): Show |
1 | a0001c0001t0001g0136 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.102-1797_102-1796i others(32): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203906 | ||||||
| chr2:74203906 | G | GTTTAGTT others(43): Show |
1 | a0001c0001t0001g0022 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.102-1797_102-1796i others(52): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203906 | ||||||
| chr2:74203906 | G | GTTTAGTT others(53): Show |
2 | a0001c0001t0001g0003 a0001c0001t0009g0003 |
2 | HG02071.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.102-1797_102-1796i others(62): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203906 | ||||||
| chr2:74203906 | G | GTTTAGTT others(54): Show |
1 | a0001c0001t0001g0003 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.102-1797_102-1796i others(63): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203906 | ||||||
| chr2:74203906 | G | GTTTAGTT others(139): Show |
1 | a0001c0001t0003g0044 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.102-1797_102-1796i others(148): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203906 | ||||||
| chr2:74203906 | G | GTTTAGTT others(164): Show |
1 | a0001c0001t0003g0044 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102-1797_102-1796i others(173): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203906 | ||||||
| chr2:74203906 | G | GTTTAGTT others(174): Show |
1 | a0001c0001t0001g0003 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.102-1797_102-1796i others(183): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203906 | ||||||
| chr2:74203906 | G | GTTTAGTT others(189): Show |
1 | a0001c0001t0001g0121 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.102-1797_102-1796i others(198): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203906 | ||||||
| chr2:74203906 | G | GTTTAGTT others(214): Show |
1 | a0001c0001t0001g0003 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.102-1797_102-1796i others(223): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203906 | ||||||
| chr2:74203906 | G | GTTTAGTT others(234): Show |
1 | a0001c0001t0001g0003 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.102-1797_102-1796i others(243): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203906 | ||||||
| chr2:74203906 | G | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0039 |
4 | HG04228.hp2 NA18953.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.102-1799G>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74203906 | |||||||
| chr2:74203909 | A | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | NA18950.hp2 NA18955.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.102-1796A>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74203909 | |||||||
| chr2:74203910 | G | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | NA18950.hp2 NA18955.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.102-1795G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74203910 | |||||||
| chr2:74203911 | T | G | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | NA18950.hp2 NA18955.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.102-1794T>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74203911 | |||||||
| chr2:74203911 | T | TTTAGTTT others(37): Show |
3 | a0001c0001t0001g0038 a0001c0001t0001g0203 a0001c0001t0019g0038 |
3 | HG02155.hp1 NA18954.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.102-1777_102-1776i others(46): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203911 | ||||||
| chr2:74203911 | T | TTTAGTTT others(42): Show |
1 | a0001c0001t0001g0132 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.102-1777_102-1776i others(51): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203911 | ||||||
| chr2:74203911 | T | TTTAGTTT others(47): Show |
1 | a0001c0001t0005g0133 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.102-1777_102-1776i others(56): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203911 | ||||||
| chr2:74203911 | T | TTTAGTTT others(57): Show |
1 | a0001c0001t0001g0134 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.102-1777_102-1776i others(66): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203911 | ||||||
| chr2:74203911 | T | TTTAGTTT others(67): Show |
2 | a0001c0001t0001g0135 a0001c0001t0001g0204 |
2 | NA19074.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.102-1777_102-1776i others(76): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203911 | ||||||
| chr2:74203911 | T | TTTAGTTT others(77): Show |
1 | a0001c0001t0001g0205 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.102-1777_102-1776i others(86): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74203911 | ||||||
| chr2:74204244 | A | G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0130 a0001c0001t0001g0142 others(3): Show |
8 | HG02027.hp2 HG02074.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-1461A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74204244 | |||||||
| chr2:74204349 | C | T | 1 | a0001c0001t0026g0220 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.102-1356C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74204349 | |||||||
| chr2:74204588 | C | T | 35 | a0001c0001t0003g0009 a0001c0001t0003g0014 a0001c0001t0003g0044 others(32): Show |
49 | HG00558.hp2 HG00597.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.102-1117C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74204588 | |||||||
| chr2:74204766 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.102-939C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74204766 | |||||||
| chr2:74204789 | G | A | 46 | a0001c0001t0003g0009 a0001c0001t0003g0014 a0001c0001t0003g0044 others(43): Show |
64 | HG00558.hp2 HG00597.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.102-916G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74204789 | |||||||
| chr2:74204819 | GTTGT | G | 13 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0028 others(10): Show |
40 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.102-871_102-868del others(4): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 74204819 | ||||||
| chr2:74204902 | C | T | 1 | a0001c0001t0027g0236 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.102-803C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74204902 | |||||||
| chr2:74204947 | A | G | 12 | a0001c0001t0004g0005 a0001c0001t0004g0112 a0001c0001t0004g0200 others(9): Show |
21 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.102-758A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74204947 | |||||||
| chr2:74204957 | C | G | 1 | a0001c0001t0002g0099 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.102-748C>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74204957 | |||||||
| chr2:74204977 | C | T | 1 | a0001c0001t0013g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.102-728C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74204977 | |||||||
| chr2:74204989 | C | T | 4 | a0001c0001t0001g0106 a0001c0001t0001g0147 a0001c0001t0001g0174 others(1): Show |
4 | HG02040.hp2 HG02165.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.102-716C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74204989 | |||||||
| chr2:74204999 | T | A | 1 | a0001c0001t0006g0015 | 4 | HG02615.hp2 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-706T>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74204999 | |||||||
| chr2:74205002 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.102-703T>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74205002 | |||||||
| chr2:74205045 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.102-660G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74205045 | |||||||
| chr2:74205058 | T | C | 2 | a0001c0001t0012g0025 a0001c0001t0027g0236 |
3 | HG02451.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.102-647T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74205058 | |||||||
| chr2:74205127 | T | C | 21 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0048 others(18): Show |
24 | HG00558.hp2 HG00597.hp2 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.102-578T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74205127 | |||||||
| chr2:74205193 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.102-512G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74205193 | |||||||
| chr2:74205322 | A | G | 67 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0006 others(64): Show |
130 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.102-383A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74205322 | |||||||
| chr2:74205328 | G | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(37): Show |
82 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.102-377G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74205328 | |||||||
| chr2:74205507 | C | T | 1 | a0001c0001t0007g0208 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.102-198C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74205507 | |||||||
| chr2:74205511 | T | C | 11 | a0001c0001t0004g0005 a0001c0001t0004g0112 a0001c0001t0004g0200 others(8): Show |
19 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.102-194T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74205511 | |||||||
| chr2:74205549 | G | T | 7 | a0001c0001t0007g0050 a0001c0001t0007g0113 a0001c0001t0007g0114 others(4): Show |
8 | HG01109.hp1 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.102-156G>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74205549 | |||||||
| chr2:74205670 | G | C | 4 | a0001c0001t0001g0136 a0001c0001t0001g0152 a0001c0001t0001g0168 others(1): Show |
4 | HG01346.hp2 HG01358.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-35G>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 1/7 | chr2 | 74205670 | |||||||
| chr2:74206094 | T | C | 1 | a0001c0001t0012g0025 | 2 | HG02451.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.286+205T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 2/7 | chr2 | 74206094 | |||||||
| chr2:74206216 | G | A | 1 | a0001c0001t0013g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.286+327G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 2/7 | chr2 | 74206216 | |||||||
| chr2:74206372 | G | A | 35 | a0001c0001t0003g0009 a0001c0001t0003g0014 a0001c0001t0003g0044 others(32): Show |
49 | HG00558.hp2 HG00597.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.286+483G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 2/7 | chr2 | 74206372 | |||||||
| chr2:74206470 | C | T | 1 | a0001c0001t0003g0198 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.286+581C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 2/7 | chr2 | 74206470 | |||||||
| chr2:74206560 | C | T | 10 | a0001c0001t0004g0005 a0001c0001t0004g0112 a0001c0001t0004g0200 others(7): Show |
17 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.286+671C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 2/7 | chr2 | 74206560 | |||||||
| chr2:74206709 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.286+820A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 2/7 | chr2 | 74206709 | |||||||
| chr2:74206730 | C | T | 11 | a0001c0001t0007g0050 a0001c0001t0007g0113 a0001c0001t0007g0114 others(8): Show |
14 | HG01109.hp1 HG02280.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.286+841C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 2/7 | chr2 | 74206730 | |||||||
| chr2:74206734 | A | G | 47 | a0001c0001t0003g0009 a0001c0001t0003g0014 a0001c0001t0003g0044 others(44): Show |
69 | HG00558.hp2 HG00597.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.286+845A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 2/7 | chr2 | 74206734 | |||||||
| chr2:74206770 | G | A | 1 | a0001c0001t0003g0190 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.286+881G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 2/7 | chr2 | 74206770 | |||||||
| chr2:74206825 | C | T | 22 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0006 others(19): Show |
68 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.287-879C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 2/7 | chr2 | 74206825 | |||||||
| chr2:74206873 | G | A | 4 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0219 others(1): Show |
6 | HG02717.hp2 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-831G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 2/7 | chr2 | 74206873 | |||||||
| chr2:74207031 | C | T | 6 | a0001c0001t0007g0050 a0001c0001t0007g0113 a0001c0001t0007g0114 others(3): Show |
7 | HG01109.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-673C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 2/7 | chr2 | 74207031 | |||||||
| chr2:74207118 | G | C | 1 | a0001c0001t0027g0236 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.287-586G>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 2/7 | chr2 | 74207118 | |||||||
| chr2:74207189 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.287-515T>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 2/7 | chr2 | 74207189 | |||||||
| chr2:74207191 | C | T | 1 | a0001c0001t0006g0015 | 4 | HG02615.hp2 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-513C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 2/7 | chr2 | 74207191 | |||||||
| chr2:74207269 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.287-435C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 2/7 | chr2 | 74207269 | |||||||
| chr2:74207364 | G | A | 1 | a0001c0001t0003g0191 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.287-340G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 2/7 | chr2 | 74207364 | |||||||
| chr2:74207543 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.287-161A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 2/7 | chr2 | 74207543 | |||||||
| chr2:74207617 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.287-87C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 2/7 | chr2 | 74207617 | |||||||
| chr2:74207864 | T | C | 1 | a0001c0001t0003g0197 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.409+38T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 3/7 | chr2 | 74207864 | |||||||
| chr2:74208031 | C | G | 5 | a0001c0001t0005g0036 a0001c0001t0005g0110 a0001c0001t0005g0179 others(2): Show |
6 | HG01891.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.409+205C>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 3/7 | chr2 | 74208031 | |||||||
| chr2:74208205 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(45): Show |
90 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.410-364A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 3/7 | chr2 | 74208205 | |||||||
| chr2:74208355 | C | A | 4 | a0001c0001t0010g0223 a0001c0001t0010g0224 a0001c0001t0010g0225 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.410-214C>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 3/7 | chr2 | 74208355 | |||||||
| chr2:74208492 | G | A | 1 | a0001c0001t0026g0220 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.410-77G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 3/7 | chr2 | 74208492 | |||||||
| chr2:74208499 | A | G | 18 | a0001c0001t0001g0042 a0001c0001t0001g0105 a0001c0001t0001g0120 others(15): Show |
19 | HG00408.hp1 HG00621.hp2 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.410-70A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 3/7 | chr2 | 74208499 | |||||||
| chr2:74208934 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.562+213C>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 4/7 | chr2 | 74208934 | |||||||
| chr2:74209098 | AG | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(174): Show |
311 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(308): Show |
intron_variant | MODIFIER | c.562+379delG | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 74209098 | ||||||
| chr2:74209100 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(174): Show |
311 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(308): Show |
intron_variant | MODIFIER | c.562+379G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 4/7 | chr2 | 74209100 | |||||||
| chr2:74209133 | G | C | 1 | a0001c0001t0001g0071 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.562+412G>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 4/7 | chr2 | 74209133 | |||||||
| chr2:74209169 | C | G | 1 | a0001c0001t0001g0076 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.562+448C>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 4/7 | chr2 | 74209169 | |||||||
| chr2:74209176 | G | T | 5 | a0001c0001t0006g0015 a0001c0001t0006g0232 a0001c0001t0006g0233 others(2): Show |
8 | HG02615.hp2 HG02965.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.562+455G>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 4/7 | chr2 | 74209176 | |||||||
| chr2:74209286 | A | G | 3 | a0001c0001t0006g0232 a0001c0001t0006g0233 a0001c0001t0006g0234 |
3 | HG03130.hp2 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.562+565A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 4/7 | chr2 | 74209286 | |||||||
| chr2:74209303 | C | T | 4 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0219 others(1): Show |
6 | HG02717.hp2 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.562+582C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 4/7 | chr2 | 74209303 | |||||||
| chr2:74209545 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.563-397G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 4/7 | chr2 | 74209545 | |||||||
| chr2:74209594 | A | G | 91 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0006 others(88): Show |
167 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.563-348A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 4/7 | chr2 | 74209594 | |||||||
| chr2:74210200 | A | G | 1 | a0001c0001t0001g0039 | 2 | HG04204.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.670+151A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | chr2 | 74210200 | |||||||
| chr2:74210427 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.670+378G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | chr2 | 74210427 | |||||||
| chr2:74210452 | A | C | 2 | a0001c0001t0003g0044 a0001c0001t0012g0025 |
4 | HG02451.hp1 HG02630.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.670+403A>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | chr2 | 74210452 | |||||||
| chr2:74210460 | C | G | 1 | a0001c0001t0027g0236 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.670+411C>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | chr2 | 74210460 | |||||||
| chr2:74210473 | T | C | 6 | a0001c0001t0007g0050 a0001c0001t0007g0113 a0001c0001t0007g0114 others(3): Show |
7 | HG01109.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.670+424T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | chr2 | 74210473 | |||||||
| chr2:74210546 | T | C | 2 | a0001c0001t0003g0044 a0001c0001t0012g0025 |
4 | HG02451.hp1 HG02630.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.670+497T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | chr2 | 74210546 | |||||||
| chr2:74210649 | T | C | 13 | a0001c0001t0007g0050 a0001c0001t0007g0113 a0001c0001t0007g0114 others(10): Show |
14 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.671-550T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | chr2 | 74210649 | |||||||
| chr2:74210673 | A | T | 1 | a0001c0001t0027g0236 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.671-526A>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | chr2 | 74210673 | |||||||
| chr2:74210785 | G | GT | 17 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0022 others(14): Show |
24 | HG01106.hp2 HG01109.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.671-397dupT | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 74210785 | ||||||
| chr2:74210785 | G | GTT | 45 | a0001c0001t0001g0210 a0001c0001t0002g0002 a0001c0001t0002g0004 others(42): Show |
103 | HG00280.hp2 HG00438.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.671-398_671-397dup others(2): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 74210785 | ||||||
| chr2:74210785 | G | GTTT | 11 | a0001c0001t0002g0028 a0001c0001t0002g0031 a0001c0001t0002g0093 others(8): Show |
16 | HG00423.hp2 HG01099.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.671-399_671-397dup others(3): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 74210785 | ||||||
| chr2:74210785 | G | GTTTTTTT others(6): Show |
1 | a0001c0001t0003g0192 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.671-404_671-403ins others(13): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 74210785 | ||||||
| chr2:74210785 | G | GTTTTTTT others(5): Show |
4 | a0001c0001t0001g0026 a0001c0001t0003g0199 a0001c0001t0010g0223 others(1): Show |
5 | HG02257.hp1 HG03195.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.671-408_671-397dup others(12): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 74210785 | ||||||
| chr2:74210785 | G | GTTTTTTT others(6): Show |
46 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(43): Show |
85 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.671-409_671-397dup others(13): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 74210785 | ||||||
| chr2:74210785 | G | GTTTTTTT others(7): Show |
27 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0059 others(24): Show |
39 | HG00597.hp1 HG00642.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.671-410_671-397dup others(14): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 74210785 | ||||||
| chr2:74210785 | G | GTTTTTTT others(8): Show |
2 | a0001c0001t0003g0047 a0001c0001t0003g0188 |
3 | HG00597.hp2 NA19002.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.671-411_671-397dup others(15): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 74210785 | ||||||
| chr2:74210785 | G | GTTTTTTT others(10): Show |
1 | a0001c0001t0013g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.671-413_671-397dup others(17): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 74210785 | ||||||
| chr2:74210868 | C | A | 3 | a0001c0001t0004g0112 a0001c0001t0004g0200 a0001c0001t0004g0202 |
3 | HG02622.hp2 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.671-331C>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | chr2 | 74210868 | |||||||
| chr2:74210872 | C | T | 1 | a0001c0001t0006g0235 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.671-327C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | chr2 | 74210872 | |||||||
| chr2:74210957 | T | C | 1 | a0001c0001t0002g0089 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.671-242T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | chr2 | 74210957 | |||||||
| chr2:74210994 | C | T | 1 | a0001c0001t0012g0025 | 2 | HG02451.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.671-205C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | chr2 | 74210994 | |||||||
| chr2:74211036 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.671-163C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | chr2 | 74211036 | |||||||
| chr2:74211052 | T | G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0130 a0001c0001t0001g0142 others(3): Show |
8 | HG02027.hp2 HG02074.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.671-147T>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | chr2 | 74211052 | |||||||
| chr2:74211189 | T | C | 4 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0219 others(1): Show |
6 | HG02717.hp2 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.671-10T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 5/7 | chr2 | 74211189 | |||||||
| chr2:74211647 | G | T | 5 | a0001c0001t0006g0015 a0001c0001t0006g0232 a0001c0001t0006g0233 others(2): Show |
8 | HG02615.hp2 HG02965.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.764-94G>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 6/7 | chr2 | 74211647 | |||||||
| chr2:74211944 | C | CT | 28 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0001g0075 others(25): Show |
38 | HG00621.hp2 HG01175.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.889+100dupT | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 74211944 | ||||||
| chr2:74211944 | C | CTT | 23 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0006 others(20): Show |
70 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.889+99_889+100dupT others(1): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 74211944 | ||||||
| chr2:74211944 | CT | C | 6 | a0001c0001t0001g0086 a0001c0001t0001g0128 a0001c0001t0001g0148 others(3): Show |
6 | HG03195.hp2 HG03669.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.889+100delT | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 74211944 | ||||||
| chr2:74212052 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.889+186C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74212052 | |||||||
| chr2:74212053 | T | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(146): Show |
271 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(268): Show |
intron_variant | MODIFIER | c.889+187T>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74212053 | |||||||
| chr2:74212147 | CCCT | C | 6 | a0001c0001t0007g0050 a0001c0001t0007g0113 a0001c0001t0007g0114 others(3): Show |
7 | HG01109.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.889+283_889+285del others(3): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 74212147 | ||||||
| chr2:74212182 | T | TTCCC | 88 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0006 others(85): Show |
164 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.889+320_889+323dup others(4): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 74212182 | ||||||
| chr2:74212246 | T | G | 1 | a0001c0001t0023g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.889+380T>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74212246 | |||||||
| chr2:74212253 | G | A | 1 | a0001c0001t0020g0085 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.889+387G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74212253 | |||||||
| chr2:74212263 | C | CT | 94 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(91): Show |
155 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.889+419dupT | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 74212263 | ||||||
| chr2:74212263 | C | CTT | 5 | a0001c0001t0001g0018 a0001c0001t0001g0087 a0001c0001t0003g0072 others(2): Show |
7 | HG02572.hp1 HG03831.hp2 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.889+418_889+419dup others(2): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 74212263 | ||||||
| chr2:74212263 | C | CTTT | 10 | a0001c0001t0004g0005 a0001c0001t0004g0112 a0001c0001t0004g0200 others(7): Show |
17 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.889+417_889+419dup others(3): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 74212263 | ||||||
| chr2:74212263 | C | T | 1 | a0001c0001t0012g0025 | 2 | HG02451.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.889+397C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74212263 | |||||||
| chr2:74212263 | CT | C | 31 | a0001c0001t0001g0138 a0001c0001t0001g0173 a0001c0001t0001g0238 others(28): Show |
81 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.889+419delT | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 74212263 | ||||||
| chr2:74212344 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.889+478C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74212344 | |||||||
| chr2:74212423 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.889+557C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74212423 | |||||||
| chr2:74212645 | A | G | 1 | a0001c0001t0001g0150 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.889+779A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74212645 | |||||||
| chr2:74212702 | T | C | 1 | a0001c0001t0002g0092 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.889+836T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74212702 | |||||||
| chr2:74212824 | C | T | 1 | a0001c0001t0012g0025 | 2 | HG02451.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.889+958C>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74212824 | |||||||
| chr2:74212895 | C | A | 1 | a0001c0001t0013g0228 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.889+1029C>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74212895 | |||||||
| chr2:74212909 | G | GT | 52 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0006 others(49): Show |
112 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.889+1054dupT | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 74212909 | ||||||
| chr2:74213176 | T | C | 1 | a0001c0001t0003g0044 | 2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.890-903T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74213176 | |||||||
| chr2:74213191 | A | C | 3 | a0001c0001t0004g0112 a0001c0001t0004g0200 a0001c0001t0004g0202 |
3 | HG02622.hp2 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.890-888A>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74213191 | |||||||
| chr2:74213200 | G | A | 1 | a0001c0001t0026g0220 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.890-879G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74213200 | |||||||
| chr2:74213270 | C | CT | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(55): Show |
67 | HG00558.hp2 HG00597.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.890-785dupT | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 74213270 | ||||||
| chr2:74213270 | C | CTT | 47 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0006 others(44): Show |
99 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.890-786_890-785dup others(2): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 74213270 | ||||||
| chr2:74213270 | C | CTTT | 15 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0029 others(12): Show |
17 | HG00423.hp2 HG00735.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.890-787_890-785dup others(3): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 74213270 | ||||||
| chr2:74213270 | C | CTTTT | 4 | a0001c0001t0003g0009 a0001c0001t0003g0045 a0001c0001t0003g0182 others(1): Show |
9 | HG00741.hp2 HG01169.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.890-788_890-785dup others(4): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 74213270 | ||||||
| chr2:74213299 | C | G | 10 | a0001c0001t0004g0005 a0001c0001t0004g0112 a0001c0001t0004g0200 others(7): Show |
17 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.890-780C>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74213299 | |||||||
| chr2:74213313 | G | C | 1 | a0001c0001t0026g0220 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.890-766G>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74213313 | |||||||
| chr2:74213339 | G | C | 92 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0006 others(89): Show |
168 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.890-740G>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74213339 | |||||||
| chr2:74213592 | T | C | 1 | a0001c0001t0008g0053 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.890-487T>C | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74213592 | |||||||
| chr2:74213619 | G | A | 1 | a0001c0001t0002g0030 | 2 | NA19009.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.890-460G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74213619 | |||||||
| chr2:74213745 | A | T | 1 | a0001c0001t0025g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.890-334A>T | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74213745 | |||||||
| chr2:74213752 | A | G | 4 | a0001c0001t0002g0004 a0001c0001t0002g0088 a0001c0001t0002g0097 others(1): Show |
16 | HG00280.hp2 HG00733.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.890-327A>G | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74213752 | |||||||
| chr2:74214000 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.890-79G>A | MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | chr2 | 74214000 | |||||||
| chr2:74214001 | CTTGT | C | 3 | a0001c0001t0014g0100 a0001c0001t0014g0227 a0001c0001t0027g0236 |
3 | HG00735.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.890-75_890-72delGT others(2): Show |
MTHFD2 | ENSG00000065911.13 | transcript | ENST00000394053.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 74214001 |